Clinical experience with acute overdose of Indaferil is limited. The administration of doses up to 48 mg of zoledronic acid in error has been reported. Patients who have received doses higher than those recommended should be carefully monitored, since renal function impairment (including renal failure) and serum electrolyte (including calcium, phosphorus and magnesium) abnormalities have been observed. In the event of hypocalcaemia, calcium gluconate infusions should be administered as clinically indicated.
Clinical experience with acute overdose of Indaferil is limited. The administration of doses up to 48 mg of Indaferil in error has been reported. Patients who have received doses higher than those recommended should be carefully monitored, since renal function impairment (including renal failure) and serum electrolyte (including calcium, phosphorus and magnesium) abnormalities have been observed. In the event of hypocalcaemia, calcium gluconate infusions should be administered as clinically indicated.
-
- Breast-feeding
This medicinal product must not be allowed to come into contact with any calcium-containing solutions and it must not be mixed or given intravenously with any other medicinal product in the same infusion line.
To avoid potential incompatibilities, Indaferil concentrate is to be diluted with 0.9% w/v sodium chloride solution or 5% w/v glucose solution.
The medicinal product must not be mixed with calcium or other divalent cation-containing infusion solutions such as lactated Ringer's solution, and should be administered as a single intravenous solution in a separate infusion line.
Summary of the safety profile
Within three days after Indaferil administration, an acute phase reaction has commonly been reported, with symptoms including bone pain, fever, fatigue, arthralgia, myalgia, rigors and arthritis with subsequent joint swelling; these symptoms usually resolve within a few days (see description of selected adverse reactions).
The following are the important identified risks with Indaferil in the approved indications:
Renal function impairment, osteonecrosis of the jaw, acute phase reaction, hypocalcaemia, atrial fibrillation, anaphylaxis, interstitial lung disease. The frequencies for each of these identified risks are shown in Table 2.
Tabulated list of adverse reactions
The following adverse reactions, listed in Table 2, have been accumulated from clinical studies and post-marketing reports following predominantly chronic treatment with 4 mg zoledronic acid:
Table 2
Adverse reactions are ranked under headings of frequency, the most frequent first, using the following convention: Very common (>1/10), common (>1/100 to <1/10), uncommon (>1/1,000 to <1/100), rare (>1/10,000 to <1/1,000), very rare (<1/10,000), not known (cannot be estimated from the available data).
| Blood and lymphatic system disorders | |
| Common: | Anaemia |
| Uncommon: | Thrombocytopenia, leukopenia |
| Rare: | Pancytopenia |
| Immune system disorders | |
| Uncommon: | Hypersensitivity reaction |
| Rare: | Angioneurotic oedema |
| Psychiatric disorders | |
| Uncommon: | Anxiety, sleep disturbance |
| Rare: | Confusion |
| Nervous system disorders | |
| Common: | Headache |
| Uncommon: | Dizziness, paraesthesia, dysgeusia, hypoaesthesia, hyperaesthesia, tremor, somnolence |
| Very rare: | Convulsions, hypoaesthesia and tetany (secondary to hypocalcaemia) |
| Eye disorders | |
| Common: | Conjunctivitis |
| Uncommon: | Blurred vision, scleritis and orbital inflammation |
| Rare: | Uveitis |
| Very rare: | Episcleritis |
| Cardiac disorders | |
| Uncommon: | Hypertension, hypotension, atrial fibrillation, hypotension leading to syncope or circulatory collapse |
| Rare: | Bradycardia, cardiac arrhythmia (secondary to hypocalcaemia) |
| Respiratory, thoracic and mediastinal disorders | |
| Uncommon: | Dyspnoea, cough, bronchoconstriction |
| Rare: | Interstitial lung disease |
| Gastrointestinal disorders | |
| Common: | Nausea, vomiting, decreased appetite |
| Uncommon: | Diarrhoea, constipation, abdominal pain, dyspepsia, stomatitis, dry mouth |
| Skin and subcutaneous tissue disorders | |
| Uncommon: | Pruritus, rash (including erythematous and macular rash), increased sweating |
| Musculoskeletal and connective tissue disorders | |
| Common: | Bone pain, myalgia, arthralgia, generalised pain |
| Uncommon: | Muscle spasms, osteonecrosis of the jaw |
| Very rare: | Osteonecrosis of the external auditory canal (bisphosphonate class adverse reaction) and other anatomical sites including femur and hip |
| Renal and urinary disorders | |
| Common: | Renal impairment |
| Uncommon: Rare: | Acute renal failure, haematuria, proteinuria Acquired Fanconi syndrome |
| General disorders and administration site conditions | |
| Common: | Fever, flu-like syndrome (including fatigue, rigors, malaise and flushing) |
| Uncommon: | Asthenia, peripheral oedema, injection site reactions (including pain, irritation, swelling, induration), chest pain, weight increase, anaphylactic reaction/shock, urticaria |
| Rare: | Arthritis and joint swelling as a symptom of acute phase reaction |
| Investigations | |
| Very common: | Hypophosphataemia |
| Common: | Blood creatinine and blood urea increased, hypocalcaemia |
| Uncommon: | Hypomagnesaemia, hypokalaemia |
| Rare: | Hyperkalaemia, hypernatraemia |
Description of selected adverse reactions
Renal function impairment
Indaferil has been associated with reports of renal dysfunction. In a pooled analysis of safety data from Indaferil registration trials for the prevention of skeletal-related events in patients with advanced malignancies involving bone, the frequency of renal impairment adverse events suspected to be related to Indaferil (adverse reactions) was as follows: multiple myeloma (3.2%), prostate cancer (3.1%), breast cancer (4.3%), lung and other solid tumours (3.2%). Factors that may increase the potential for deterioration in renal function include dehydration, pre-existing renal impairment, multiple cycles of Indaferil or other bisphosphonates, as well as concomitant use of nephrotoxic medicinal products or using a shorter infusion time than currently recommended. Renal deterioration, progression to renal failure and dialysis have been reported in patients after the initial dose or a single dose of 4 mg zoledronic acid.
Osteonecrosis of the jaw
Cases of osteonecrosis of the jaw have been reported, predominantly in cancer patients treated with medicinal products that inhibit bone resorption, such as Indaferil. Many of these patients were also receiving chemotherapy and corticosteroids and had signs of local infection including osteomyelitis. The majority of the reports refer to cancer patients following tooth extractions or other dental surgeries.
Atrial fibrillation
In one 3-year, randomised, double-blind controlled trial that evaluated the efficacy and safety of zoledronic acid 5 mg once yearly vs. placebo in the treatment of postmenopausal osteoporosis (PMO), the overall incidence of atrial fibrillation was 2.5% (96 out of 3,862) and 1.9% (75 out of 3,852) in patients receiving zoledronic acid 5 mg and placebo, respectively. The rate of atrial fibrillation serious adverse events was 1.3% (51 out of 3,862) and 0.6% (22 out of 3,852) in patients receiving zoledronic acid 5 mg and placebo, respectively. The imbalance observed in this trial has not been observed in other trials with zoledronic acid, including those with Indaferil (zoledronic acid) 4 mg every 3-4 weeks in oncology patients. The mechanism behind the increased incidence of atrial fibrillation in this single clinical trial is unknown.
Acute phase reaction
This adverse drug reaction consists of a constellation of symptoms that includes fever, myalgia, headache, extremity pain, nausea, vomiting, diarrhoea arthralgia and arthritis with subsequent joint swelling. The onset time is ≤ 3 days post-Indaferil infusion, and the reaction is also referred to using the terms “flu-like†or “post-dose†symptoms.
Atypical fractures of the femur
During post-marketing experience the following reactions have been reported (frequency rare):
Atypical subtrochanteric and diaphyseal femoral fractures (bisphopsphonate class adverse reaction).
Hypocalcaemia-related ADRs
Hypocalcaemia is an important identified risk with Indaferil in the approved indications. Based on the review of both clinical trial and post-marketing cases, there is sufficient evidence to support an association between Indaferil therapy, the reported event of hypocalcaemia, and the secondary development of cardiac arrhythmia. Furthermore, there is evidence of an association between hypocalcaemia and secondary neurological events reported in these cases including; convulsions, hypoaesthesia and tetany.
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.
Summary of the safety profile
Within three days after Indaferil administration, an acute phase reaction has commonly been reported, with symptoms including bone pain, fever, fatigue, arthralgia, myalgia, rigors and arthritis with subsequent joint swelling; these symptoms usually resolve within a few days (see description of selected adverse reactions).
The following are the important identified risks with Indaferil in the approved indications:
Renal function impairment, osteonecrosis of the jaw, acute phase reaction, hypocalcaemia, atrial fibrillation, anaphylaxis, interstitial lung disease. The frequencies for each of these identified risks are shown in Table 1.
Tabulated list of adverse reactions
The following adverse reactions, listed in Table 1, have been accumulated from clinical studies and post-marketing reports following predominantly chronic treatment with 4 mg Indaferil:
Table 1
Adverse reactions are ranked under headings of frequency, the most frequent first, using the following convention: Very common (>1/10), common (>1/100, <1/10), uncommon (>1/1,000, <1/100), rare (>1/10,000, <1/1,000), very rare (<1/10,000), not known (cannot be estimated from the available data).
| Blood and lymphatic system disorders |
|
| Common: | Anaemia |
| Uncommon: | Thrombocytopenia, leukopenia |
| Rare: | Pancytopenia |
| Immune system disorders |
|
| Uncommon: | Hypersensitivity reaction |
| Rare: | Angioneurotic oedema |
| Psychiatric disorders |
|
| Uncommon: | Anxiety, sleep disturbance |
| Rare: | Confusion |
| Nervous system disorders |
|
| Common: | Headache |
| Uncommon: | Dizziness, paraesthesia, dysgeusia, hypoaesthesia, hyperaesthesia, tremor, somnolence |
| Very rare: | Convulsions, hypoaesthesia and tetany (secondary to hypocalcaemia) |
| Eye disorders |
|
| Common: | Conjunctivitis |
| Uncommon: | Blurred vision, scleritis and orbital inflammation |
| Rare | Uveitis |
| Very rare: | Episcleritis |
| Cardiac disorders | |
| Uncommon: | Hypertension, hypotension, atrial fibrillation, hypotension leading to syncope or circulatory collapse |
| Rare: | Bradycardia, cardiac arrhythmia (secondary to hypocalcaemia) |
| Respiratory, thoracic and mediastinal disorders | |
| Uncommon: | Dyspnoea, cough, bronchoconstriction |
| Rare: | Interstitial lung disease |
| Gastrointestinal disorders | |
| Common: | Nausea, vomiting, decreased appetite |
| Uncommon: | Diarrhoea, constipation, abdominal pain, dyspepsia, stomatitis, dry mouth |
| Skin and subcutaneous tissue disorders | |
| Uncommon: | Pruritus, rash (including erythematous and macular rash), increased sweating |
| Musculoskeletal and connective tissue disorders | |
| Common: | Bone pain, myalgia, arthralgia, generalized pain |
| Uncommon: | Muscle spasms, osteonecrosis of the jaw |
| Very rare: | Osteonecrosis of the external auditory canal (bisphosphonate class adverse reaction) and other anatomical sites including femur and hip |
| Renal and urinary disorders |
|
| Common: | Renal impairment |
| Uncommon: | Acute renal failure, haematuria, proteinuria |
| Rare: | Acquired Fanconi syndrome |
| General disorders and administration site conditions |
|
| Common: | Fever, flu-like syndrome (including fatigue, rigors, malaise and flushing) |
| Uncommon: | Asthenia, peripheral oedema, injection site reactions (including pain, irritation, swelling, induration), chest pain, weight increase, anaphylactic reaction/shock, urticaria |
| Rare: | Arthritis and joint swelling as a symptom of acute phase reaction |
| Investigations |
|
| Very common: | Hypophosphataemia |
| Common: | Blood creatinine and blood urea increased, hypocalcaemia |
| Uncommon: | Hypomagnesaemia, hypokalaemia |
| Rare: | Hyperkalaemia, hypernatraemia |
Description of selected adverse reactions
Renal function impairment
Indaferil has been associated with reports of renal dysfunction. In a pooled analysis of safety data from Indaferil registration trials for the prevention of skeletal-related events in patients with advanced malignancies involving bone, the frequency of renal impairment adverse events suspected to be related to Indaferil (adverse reactions) was as follows: multiple myeloma (3.2%), prostate cancer (3.1%), breast cancer (4.3%), lung and other solid tumours (3.2%). Factors that may increase the potential for deterioration in renal function include dehydration, pre-existing renal impairment, multiple cycles of Indaferil or other bisphosphonates, as well as concomitant use of nephrotoxic medicinal products or using a shorter infusion time than currently recommended. Renal deterioration, progression to renal failure and dialysis have been reported in patients after the initial dose or a single dose of 4 mg Indaferil.
Osteonecrosis of the jaw
Cases of osteonecrosis of the jaw have been reported, predominantly in cancer patients treated with medicinal products that inhibit bone resorption, such as Indaferil. Many of these patients were also receiving chemotherapy and corticosteroids and had signs of local infection including osteomyelitis. The majority of the reports refer to cancer patients following tooth extractions or other dental surgeries.
Atrial fibrillation
In one 3-year, randomised, double-blind controlled trial that evaluated the efficacy and safety of Indaferil 5 mg once yearly vs. placebo in the treatment of postmenopausal osteoporosis (PMO), the overall incidence of atrial fibrillation was 2.5% (96 out of 3,862) and 1.9% (75 out of 3,852) in patients receiving Indaferil 5 mg and placebo, respectively. The rate of atrial fibrillation serious adverse events was 1.3% (51 out of 3,862) and 0.6% (22 out of 3,852) in patients receiving Indaferil 5 mg and placebo, respectively. The imbalance observed in this trial has not been observed in other trials with Indaferil, including those with Indaferil 4 mg every 3-4 weeks in oncology patients. The mechanism behind the increased incidence of atrial fibrillation in this single clinical trial is unknown.
Acute phase reaction
This adverse drug reaction consists of a constellation of symptoms that includes fever, myalgia, headache, extremity pain, nausea, vomiting, diarrhoea, arthralgia and arthritis with subsequent joint swelling. The onset time is ≤ 3 days post-Indaferil infusion, and the reaction is also referred to using the terms “flu-like†or “post-dose†symptoms.
Atypical fractures of the femur
During post-marketing experience the following reactions have been reported (frequency rare): Atypical subtrochanteric and diaphyseal femoral fractures (bisphosphonate class adverse reaction).
Hypocalcaemia-related ADRs
Hypocalcaemia is an important identified risk with Indaferil in the approved indications. Based on the review of both clinical trial and post-marketing cases, there is sufficient evidence to support an association between Indaferil therapy, the reported event of hypocalcaemia, and the secondary development of cardiac arrhythmia. Furthermore, there is evidence of an association between hypocalcaemia and secondary neurological events reported in these cases including; convulsions, hypoaesthesia and tetany.
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard.
Acute toxicity
The highest non-lethal single intravenous dose was 10 mg/kg bodyweight in mice and 0.6 mg/kg in rats.
Subchronic and chronic toxicity
Zoledronic acid was well tolerated when administered subcutaneously to rats and intravenously to dogs at doses up to 0.02 mg/kg daily for 4 weeks. Administration of 0.001 mg/kg/day subcutaneously in rats and 0.005 mg/kg intravenously once every 2-3 days in dogs for up to 52 weeks was also well tolerated.
The most frequent finding in repeat-dose studies consisted of increased primary spongiosa in the metaphyses of long bones in growing animals at nearly all doses, a finding that reflected the compound's pharmacological antiresorptive activity.
The safety margins relative to renal effects were narrow in the long-term repeat-dose parenteral animal studies but the cumulative no adverse event levels (NOAELs) in the single dose (1.6 mg/kg) and multiple dose studies of up to one month (0.06-0.6 mg/kg/day) did not indicate renal effects at doses equivalent to or exceeding the highest intended human therapeutic dose. Longer-term repeat administration at doses bracketing the highest intended human therapeutic dose of zoledronic acid produced toxicological effects in other organs, including the gastrointestinal tract, liver, spleen and lungs, and at intravenous injection sites.
Reproduction toxicity
Zoledronic acid was teratogenic in the rat at subcutaneous doses > 0.2 mg/kg. Although no teratogenicity or foetotoxicity was observed in the rabbit, maternal toxicity was found. Dystocia was observed at the lowest dose (0.01 mg/kg bodyweight) tested in the rat.
Mutagenicity and carcinogenic potential
Zoledronic acid was not mutagenic in the mutagenicity tests performed and carcinogenicity testing did not provide any evidence of carcinogenic potential.
Acute toxicity
The highest non-lethal single intravenous dose was 10 mg/kg bodyweight in mice and 0.6 mg/kg in rats.
Subchronic and chronic toxicity
Indaferil was well tolerated when administered subcutaneously to rats and intravenously to dogs at doses up to 0.02 mg/kg daily for 4 weeks. Administration of 0.001 mg/kg/day subcutaneously in rats and 0.005 mg/kg intravenously once every 2-3 days in dogs for up to 52 weeks was also well tolerated.
The most frequent finding in repeat-dose studies consisted of increased primary spongiosa in the metaphyses of long bones in growing animals at nearly all doses, a finding that reflected the compound's pharmacological antiresorptive activity.
The safety margins relative to renal effects were narrow in the long-term repeat-dose parenteral animal studies but the cumulative no adverse event levels (NOAELs) in the single dose (1.6 mg/kg) and multiple dose studies of up to one month (0.06-0.6 mg/kg/day) did not indicate renal effects at doses equivalent to or exceeding the highest intended human therapeutic dose. Longer-term repeat administration at doses bracketing the highest intended human therapeutic dose of Indaferil produced toxicological effects in other organs, including the gastrointestinal tract, liver, spleen and lungs, and at intravenous injection sites.
Reproduction toxicity
Indaferil was teratogenic in the rat at subcutaneous doses > 0.2 mg/kg. Although no teratogenicity or foetotoxicity was observed in the rabbit, maternal toxicity was found. Dystocia was observed at the lowest dose (0.01 mg/kg bodyweight) tested in the rat.
Mutagenicity and carcinogenic potential
Indaferil was not mutagenic in the mutagenicity tests performed and carcinogenicity testing did not provide any evidence of carcinogenic potential.
- Prevention of skeletal related events (pathological fractures, spinal compression, radiation or surgery to bone, or tumour-induced hypercalcaemia) in adult patients with advanced malignancies involving bone.
- Treatment of adult patients with tumour-induced hypercalcaemia (TIH).
- Prevention of skeletal related events (pathological fractures, spinal compression, radiation or surgery to bone, or tumour-induced hypercalcaemia) in adult patients with advanced malignancies involving bone.
- Treatment of adult patients with tumour-induced hypercalcaemia (TIH).
Pharmacotherapeutic group: Drugs for treatment of bone diseases, bisphosphonates, ATC code: M05BA08
Zoledronic acid belongs to the class of bisphosphonates and acts primarily on bone. It is an inhibitor of osteoclastic bone resorption.
The selective action of bisphosphonates on bone is based on their high affinity for mineralised bone, but the precise molecular mechanism leading to the inhibition of osteoclastic activity is still unclear. In long-term animal studies, zoledronic acid inhibits bone resorption without adversely affecting the formation, mineralisation or mechanical properties of bone.
In addition to being a potent inhibitor of bone resorption, zoledronic acid also possesses several anti-tumour properties that could contribute to its overall efficacy in the treatment of metastatic bone disease. The following properties have been demonstrated in preclinical studies:
- In vivo: Inhibition of osteoclastic bone resorption, which alters the bone marrow microenvironment, making it less conducive to tumour cell growth, anti-angiogenic activity and anti-pain activity.
- In vitro: Inhibition of osteoblast proliferation, direct cytostatic and pro-apoptotic activity on tumour cells, synergistic cytostatic effect with other anti-cancer drugs, anti-adhesion/invasion activity.
Clinical trial results in the prevention of skeletal related events in patients with advanced malignancies involving bone
The first randomised, double-blind, placebo-controlled study compared zoledronic acid 4 mg to placebo for the prevention of skeletal related events (SREs) in prostate cancer patients. Zoledronic acid 4 mg significantly reduced the proportion of patients experiencing at least one skeletal related event (SRE), delayed the median time to first SRE by > 5 months, and reduced the annual incidence of events per patient - skeletal morbidity rate. Multiple event analysis showed a 36% risk reduction in developing SREs in the zoledronic acid 4 mg group compared with placebo. Patients receiving zoledronic acid 4 mg reported less increase in pain than those receiving placebo, and the difference reached significance at months 3, 9, 21 and 24. Fewer zoledronic acid 4 mg patients suffered pathological fractures. The treatment effects were less pronounced in patients with blastic lesions. Efficacy results are provided in Table 3.
In a second study including solid tumours other than breast or prostate cancer, zoledronic acid 4 mg significantly reduced the proportion of patients with an SRE, delayed the median time to first SRE by > 2 months, and reduced the skeletal morbidity rate. Multiple event analysis showed 30.7% risk reduction in developing SREs in the zoledronic acid 4 mg group compared with placebo. Efficacy results are provided in Table 4.
| Table 3: Efficacy results (prostate cancer patients receiving hormonal therapy) | ||||||
| Any SRE (+TIH) | Fractures* | Radiation therapy to bone | ||||
| zoledronic acid 4 mg | Placebo | zoledronic acid 4 mg | Placebo | zoledronic acid 4 mg | Placebo | |
| N | 214 | 208 | 214 | 208 | 214 | 208 |
| Proportion of patients with SREs (%) | 38 | 49 | 17 | 25 | 26 | 33 |
| p-value | 0.028 | 0.052 | 0.119 | |||
| Median time to SRE (days) | 488 | 321 | NR | NR | NR | 640 |
| p-value | 0.009 | 0.020 | 0.055 | |||
| Skeletal morbidity rate | 0.77 | 1.47 | 0.20 | 0.45 | 0.42 | 0.89 |
| p-value | 0.005 | 0.023 | 0.060 | |||
| Risk reduction of suffering from multiple events** (%) | 36 | - | NA | NA | NA | NA |
| p-value | 0.002 | NA | NA | |||
* Includes vertebral and non-vertebral fractures
** Accounts for all skeletal events, the total number as well as time to each event during the trial
NR Not Reached
NA Not Applicable
| Table 4: Efficacy results (solid tumours other than breast or prostate cancer) | |||||||||
| Any SRE (+TIH) | Fractures* | Radiation therapy to bone | |||||||
| zoledronic acid 4 mg | Placebo | zoledronic acid 4 mg | Placebo | zoledronic acid 4 mg | Placebo | ||||
| N | 257 | 250 | 257 | 250 | 257 | 250 | |||
| Proportion of patients with SREs (%) | 39 | 48 | 16 | 22 | 29 | 34 | |||
| p-value | 0.039 | 0.064 | 0.173 | ||||||
| Median time to SRE (days) | 236 | 155 | NR | NR | 424 | 307 | |||
| p-value | 0.009 | 0.020 | 0.079 | ||||||
| Skeletal morbidity rate | 1.74 | 2.71 | 0.39 | 0.63 | 1.24 | 1.89 | |||
| p-value | 0.012 | 0.066 | 0.099 | ||||||
| Risk reduction of suffering from multiple events** (%) | 30.7 | - | NA | NA | NA | NA | |||
| p-value | 0.003 | NA | NA | ||||||
* Includes vertebral and non-vertebral fractures
** Accounts for all skeletal events, the total number as well as time to each event during the trial
NR Not Reached
NA Not Applicable
In a third phase III randomised, double-blind trial, zoledronic acid 4 mg or 90 mg pamidronate every 3 to 4 weeks were compared in patients with multiple myeloma or breast cancer with at least one bone lesion. The results demonstrated that zoledronic acid 4 mg showed comparable efficacy to 90 mg pamidronate in the prevention of SREs. The multiple event analysis revealed a significant risk reduction of 16% in patients treated with zoledronic acid 4 mg in comparison with patients receiving pamidronate. Efficacy results are provided in Table 5.
| Table 5: Efficacy results (breast cancer and multiple myeloma patients) | ||||||
| Any SRE (+TIH) | Fractures* | Radiation therapy to bone | ||||
| zoledronic acid 4 mg | Pam 90 mg | zoledronic acid 4 mg | Pam 90 mg | zoledronic acid 4 mg | Pam 90 mg | |
| N | 561 | 555 | 561 | 555 | 561 | 555 |
| Proportion of patients with SREs (%) | 48 | 52 | 37 | 39 | 19 | 24 |
| p-value | 0.198 | 0.653 | 0.037 | |||
| Median time to SRE (days) | 376 | 356 | NR | 714 | NR | NR |
| p-value | 0.151 | 0.672 | 0.026 | |||
| Skeletal morbidity rate | 1.04 | 1.39 | 0.53 | 0.60 | 0.47 | 0.71 |
| p-value | 0.084 | 0.614 | 0.015 | |||
| Risk reduction of suffering from multiple events** (%) | 16 | - | NA | NA | NA | NA |
| p-value | 0.030 | NA | NA | |||
* Includes vertebral and non-vertebral fractures
** Accounts for all skeletal events, the total number as well as time to each event during the trial
NR Not Reached
NA Not Applicable
Zoledronic acid 4 mg was also studied in a double-blind, randomised, placebo-controlled trial in 228 patients with documented bone metastases from breast cancer to evaluate the effect of 4 mg zoledronic acid on the skeletal related event (SRE) rate ratio, calculated as the total number of SRE events (excluding hypercalcaemia and adjusted for prior fracture), divided by the total risk period. Patients received either 4 mg zoledronic acid or placebo every four weeks for one year. Patients were evenly distributed between zoledronic acid-treated and placebo groups.
The SRE rate (events/person year) was 0.628 for zoledronic acid and 1.096 for placebo. The proportion of patients with at least one SRE (excluding hypercalcaemia) was 29.8% in the zoledronic acid-treated group versus 49.6% in the placebo group (p=0.003). Median time to onset of the first SRE was not reached in the zoledronic acid-treated arm at the end of the study and was significantly prolonged compared to placebo (p=0.007). Zoledronic acid 4 mg reduced the risk of SREs by 41% in a multiple event analysis (risk ratio=0.59, p=0.019) compared with placebo.
In the zoledronic acid-treated group, statistically significant improvement in pain scores (using the Brief Pain Inventory, BPI) was seen at 4 weeks and at every subsequent time point during the study, when compared to placebo (Figure 1). The pain score for zoledronic acid was consistently below baseline and pain reduction was accompanied by a trend in reduced analgesics score.
Figure 1: Mean changes from baseline in BPI scores. Statistically significant differences are marked (*p<0.05) for between treatment comparisons (4 mg zoledronic acid vs. placebo)
Clinical trial results in the treatment of TIH
Clinical studies in tumour-induced hypercalcaemia (TIH) demonstrated that the effect of zoledronic acid is characterised by decreases in serum calcium and urinary calcium excretion. In Phase I dose finding studies in patients with mild to moderate tumour-induced hypercalcaemia (TIH), effective doses tested were in the range of approximately 1.2-2.5 mg.
To assess the effects of 4 mg zoledronic acid versus pamidronate 90 mg, the results of two pivotal multicentre studies in patients with TIH were combined in a pre-planned analysis. There was faster normalisation of corrected serum calcium at day 4 for 8 mg zoledronic acid and at day 7 for 4 mg and 8 mg zoledronic acid. The following response rates were observed:
Table 6: Proportion of complete responders by day in the combined TIH studies
| Day 4 | Day 7 | Day 10 | |
| Zoledronic acid 4 mg (N=86) | 45.3% (p=0.104) | 82.6% (p=0.005)* | 88.4% (p=0.002)* |
| Zoledronic acid 8 mg (N=90) | 55.6% (p=0.021)* | 83.3% (p=0.010)* | 86.7% (p=0.015)* |
| Pamidronate 90 mg (N=99) | 33.3% | 63.6% | 69.7% |
| *p-values compared to pamidronate. | |||
Median time to normocalcaemia was 4 days. Median time to relapse (re-increase of albumin-corrected serum calcium > 2.9 mmol/l) was 30 to 40 days for patients treated with zoledronic acid versus 17 days for those treated with pamidronate 90 mg (p-values: 0.001 for 4 mg and 0.007 for 8 mg zoledronic acid). There were no statistically significant differences between the two zoledronic acid doses.
In clinical trials 69 patients who relapsed or were refractory to initial treatment (zoledronic acid 4 mg, 8 mg or pamidronate 90 mg) were retreated with 8 mg zoledronic acid. The response rate in these patients was about 52%. Since those patients were retreated with the 8 mg dose only, there are no data available allowing comparison with the 4 mg zoledronic acid dose.
In clinical trials performed in patients with tumour-induced hypercalcaemia (TIH), the overall safety profile amongst all three treatment groups (zoledronic acid 4 and 8 mg and pamidronate 90 mg) was similar in types and severity.
Paediatric population
Clinical trial results in the treatment of severe osteogenesis imperfecta in paediatric patients aged 1 to 17 years
The effects of intravenous zoledronic acid in the treatment of paediatric patients (age 1 to 17 years) with severe osteogenesis imperfecta (types I, III and IV) were compared to intravenous pamidronate in one international, multicentre, randomised, open-label study with 74 and 76 patients in each treatment group, respectively. The study treatment period was 12 months preceded by a 4- to 9-week screening period during which vitamin D and elemental calcium supplements were taken for at least 2 weeks. In the clinical programme patients aged 1 to < 3 years received 0.025 mg/kg zoledronic acid (up to a maximum single dose of 0.35 mg) every 3 months and patients aged 3 to 17 years received 0.05 mg/kg zoledronic acid (up to a maximum single dose of 0.83 mg) every 3 months. An extension study was conducted in order to examine the long-term general and renal safety of once yearly or twice yearly zoledronic acid over the 12-month extension treatment period in children who had completed one year of treatment with either zoledronic acid or pamidronate in the core study.
The primary endpoint of the study was the percent change from baseline in lumbar spine bone mineral density (BMD) after 12 months of treatment. Estimated treatment effects on BMD were similar, but the trial design was not sufficiently robust to establish non-inferior efficacy for zoledronic acid. In particular there was no clear evidence of efficacy on incidence of fracture or on pain. Fracture adverse events of long bones in the lower extremities were reported in approximately 24% (femur) and 14% (tibia) of zoledronic acid-treated patients vs 12% and 5% of pamidronate-treated patients with severe osteogenesis imperfecta, regardless of disease type and causality but overall incidence of fractures was comparable for the zoledronic acid and pamidronate-treated patients: 43% (32/74) vs 41% (31/76). Interpretation of the risk of fracture is confounded by the fact that fractures are common events in patients with severe osteogenesis imperfecta as part of the disease process.
The type of adverse reactions observed in this population were similar to those previously seen in adults with advanced malignancies involving the bone. The adverse reactions ranked under headings of frequency, are presented in Table 7. The following conventional classification is used: very common (>1/10), common (>1/100 to <1/10), uncommon (>1/1,000 to <1/100), rare (>1/10,000 to <1/1,000), very rare (<1/10,000), not known (cannot be estimated from the available data).
Table 7: Adverse reactions observed in paediatric patients with severe osteogenesis imperfecta1
| Nervous system disorders | |
| Common: | Headache |
| Cardiac disorders | |
| Common: | Tachycardia |
| Respiratory, thoracic and mediastinal disorders | |
| Common: | Nasopharyngitis |
| Gastrointestinal disorders | |
| Very common: | Vomiting, nausea |
| Common: | Abdominal pain |
| Musculoskeletal and connective tissue disorders | |
| Common: | Pain in extremities, arthralgia, musculoskeletal pain |
| General disorders and administration site conditions | |
| Very common: | Pyrexia, fatigue |
| Common: | Acute phase reaction, pain |
| Investigations | |
| Very common: | Hypocalcaemia |
| Common: | Hypophosphataemia |
1 Adverse events occurring with frequencies < 5% were medically assessed and it was shown that these cases are consistent with the well established safety profile of Indaferil
In paediatric patients with severe osteogenesis imperfecta, zoledronic acid seems to be associated with more pronounced risks for acute phase reaction, hypocalcaemia and unexplained tachycardia, in comparison to pamidronate, but this difference declined after subsequent infusions.
Pharmacotherapeutic group: Drugs for treatment of bone diseases, bisphosphonates, ATC code: M05 BA 08.
Indaferil belongs to the class of bisphosphonates and acts primarily on bone. It is an inhibitor of osteoclastic bone resorption.
The selective action of bisphosphonates on bone is based on their high affinity for mineralised bone, but the precise molecular mechanism leading to the inhibition of osteoclastic activity is still unclear. In long-term animal studies, Indaferil inhibits bone resorption without adversely affecting the formation, mineralisation or mechanical properties of bone.
In addition to being a potent inhibitor of bone resorption, Indaferil also possesses several antitumour properties that could contribute to its overall efficacy in the treatment of metastatic bone disease. The following properties have been demonstrated in preclinical studies:
- In vivo: Inhibition of osteoclastic bone resorption, which alters the bone marrow microenvironment, making it less conducive to tumour cell growth, anti-angiogenic activity and anti-pain activity.
- In vitro: Inhibition of osteoblast proliferation, direct cytostatic and pro-apoptotic activity on tumour cells, synergistic cytostatic effect with other anti-cancer drugs, anti-adhesion/invasion activity.
Clinical trial results in the prevention of skeletal related events in patients with advanced malignancies involving bone
The first randomised, double-blind, placebo-controlled study compared Indaferil 4 mg to placebo for the prevention of skeletal related events (SREs) in prostate cancer patients. Indaferil 4 mg significantly reduced the proportion of patients experiencing at least one skeletal related event (SRE), delayed the median time to first SRE by > 5 months, and reduced the annual incidence of events per patient - skeletal morbidity rate. Multiple event analysis showed a 36% risk reduction in developing SREs in the Indaferil group compared with placebo. Patients receiving Indaferil reported less increase in pain than those receiving placebo, and the difference reached significance at months 3, 9, 21 and 24. Fewer Indaferil patients suffered pathological fractures. The treatment effects were less pronounced in patients with blastic lesions. Efficacy results are provided in Table 2.
In a second study including solid tumours other than breast or prostate cancer, Indaferil 4 mg significantly reduced the proportion of patients with an SRE, delayed the median time to first SRE by > 2 months, and reduced the skeletal morbidity rate. Multiple event analysis showed 30.7% risk reduction in developing SREs in the Indaferil group compared with placebo. Efficacy results are provided in Table 3.
Table 2: Efficacy results (prostate cancer patients receiving hormonal therapy)
|
| Any SRE (+TIH) | Fractures * | Radiation therapy to bone | |||
| Indaferil 4 mg | Placebo | Indaferil 4 mg | Placebo | Indaferil 4 mg | Placebo | |
| N | 214 | 208 | 214 | 208 | 214 | 208 |
| Proportion of patients with SREs (%) | 38 | 49 | 17 | 25 | 26 | 33 |
| p-value | 0.028 | 0.052 | 0.119 | |||
| Median time to SRE (days) | 488 | 321 | NR | NR | NR | 640 |
| p-value | 0.009 | 0.020 | 0.055 | |||
| Skeletal morbidity rate | 0.77 | 1.47 | 0.20 | 0.45 | 0.42 | 0.89 |
| p-value | 0.005 | 0.023 | 0.060 | |||
| Risk reduction of suffering from multiple events **(%) | 36 | - | NA | NA | NA | NA |
| p-value | 0.002 | NA | NA | |||
* Includes vertebral and non-vertebral fractures
** Accounts for all skeletal events, the total number as well as time to each event during the trial
NR Not Reached
NA Not Applicable
Table 3: Efficacy results (solid tumours other than breast or prostate cancer)
|
| Any SRE (+TIH) | Fractures * | Radiation therapy to bone | |||
| Indaferil 4 mg | Placebo | Indaferil 4 mg | Placebo | Indaferil 4 mg | Placebo | |
| N | 257 | 250 | 257 | 250 | 257 | 250 |
| Proportion of patients with SREs (%) | 39 | 48 | 16 | 22 | 29 | 34 |
| p-value | 0.039 | 0.064 | 0.173 | |||
| Median time to SRE (days) | 236 | 155 | NR | NR | 424 | 307 |
| p-value | 0.009 | 0.020 | 0.079 | |||
| Skeletal morbidity rate | 1.74 | 2.71 | 0.39 | 0.63 | 1.24 | 1.89 |
| p-value | 0.012 | 0.066 | 0.099 | |||
| Risk reduction of suffering from multiple events **(%) | 30.7 | - | NA | NA | NA | NA |
| p-value | 0.003 | NA | NA | |||
* Includes vertebral and non-vertebral fractures
** Accounts for all skeletal events, the total number as well as time to each event during the trial
NR Not Reached
NA Not Applicable
In a third phase III randomised, double-blind trial, 4 mg Indaferil or 90 mg pamidronate every 3 to 4 weeks were compared in patients with multiple myeloma or breast cancer with at least one bone lesion. The results demonstrated that Indaferil 4 mg showed comparable efficacy to 90 mg pamidronate in the prevention of SREs. The multiple event analysis revealed a significant risk reduction of 16% in patients treated with Indaferil 4 mg in comparison with patients receiving pamidronate. Efficacy results are provided in Table 4.
Table 4: Efficacy results (breast cancer and multiple myeloma patients)
|
| Any SRE (+TIH) | Fractures * | Radiation therapy to bone | |||
| Indaferil 4 mg | Placebo | Indaferil 4 mg | Placebo | Indaferil 4 mg | Placebo | |
| N | 561 | 555 | 561 | 555 | 561 | 555 |
| Proportion of patients with SREs (%) | 48 | 52 | 37 | 39 | 19 | 24 |
| p-value | 0.198 | 0.653 | 0.037 | |||
| Median time to SRE (days) | 376 | 356 | NR | 714 | NR | NR |
| p-value | 0.151 | 0.672 | 0.026 | |||
| Skeletal morbidity rate | 1.04 | 1.39 | 0.53 | 0.60 | 0.47 | 0.71 |
| p-value | 0.084 | 0.614 | 0.015 | |||
| Risk reduction of suffering from multiple events **(%) | 16 | - | NA | NA | NA | NA |
| p-value | 0.030 | NA | NA | |||
* Includes vertebral and non-vertebral fractures
** Accounts for all skeletal events, the total number as well as time to each event during the trial
NR Not Reached
NA Not Applicable
Indaferil was also studied in a double-blind, randomised, placebo-controlled trial in 228 patients with documented bone metastases from breast cancer to evaluate the effect of Indaferil on the skeletal related event (SRE) rate ratio, calculated as the total number of SRE events (excluding hypercalcaemia and adjusted for prior fracture), divided by the total risk period. Patients received either 4 mg Indaferil or placebo every four weeks for one year. Patients were evenly distributed between Indaferil -treated and placebo groups.
The SRE rate (events/person year) was 0.628 for Indaferil and 1.096 for placebo. The proportion of patients with at least one SRE (excluding hypercalcaemia) was 29.8% in the Indaferil treated group versus 49.6% in the placebo group (p=0.003). Median time to onset of the first SRE was not reached in the Indaferil treated arm at the end of the study and was significantly prolonged compared to placebo (p=0.007). Indaferil reduced the risk of SREs by 41% in a multiple event analysis (risk ratio=0.59, p=0.019) compared with placebo.
In the Indaferil treated group, statistically significant improvement in pain scores (using the Brief Pain Inventory, BPI) was seen at 4 weeks and at every subsequent time point during the study, when compared to placebo (Figure 1). The pain score for Indaferil was consistently below baseline and pain reduction was accompanied by a trend in reduced analgesics score.
Figure 1: Mean changes from baseline in BPI scores. Statistically significant differences are marked.
(*p<0.05) for between treatment comparisons (4 mg Indaferil vs. Placebo)
Clinical trial results in the treatment of TIH
Clinical studies in tumour-induced hypercalcaemia (TIH) demonstrated that the effect of Indaferil is characterised by decreases in serum calcium and urinary calcium excretion. In Phase I dose finding studies in patients with mild to moderate tumour-induced hypercalcaemia (TIH), effective doses tested were in the range of approximately 1.2-2.5 mg.
To assess the effects of 4 mg Indaferil versus pamidronate 90 mg, the results of two pivotal multicentre studies in patients with TIH were combined in a pre-planned analysis. There was faster normalisation of corrected serum calcium at day 4 for Indaferil 8 mg and at day 7 for Indaferil 4 mg and 8 mg. The following response rates were observed:
Table 5: Proportion of complete responders by day in the combined TIH studies
|
| Day 4 | Day 7 | Day 10 |
| Indaferil 4 mg (N=86) | 45.3 % (p=0.104) | 82.6% (p=0.005)* | 88.4% (p=0.002)* |
| Indaferil 8 mg (N=90) | 55.6% (p=0.021)* | 83.3% (p=0.010)* | 86.7% (p=0.015)* |
| Pamidronate 90 mg (N=99) | 33.3 % | 63.6 % | 69.7% |
| *p-values compared to pamidronate | |||
Median time to normocalcaemia was 4 days. Median time to relapse (re-increase of albumin-corrected serum calcium > 2.9 mmol/l) was 30 to 40 days for patients treated with Indaferil versus 17 days for those treated with pamidronate 90 mg (p-values: 0.001 for 4 mg and 0.007 for 8 mg Indaferil). There were no statistically significant differences between the two Indaferil doses.
In clinical trials 69 patients who relapsed or were refractory to initial treatment (Indaferil 4 mg, 8 mg or pamidronate 90 mg) were retreated with Indaferil 8 mg. The response rate in these patients was about 52%. Since those patients were retreated with the 8 mg dose only, there are no data available allowing comparison with the 4 mg Indaferil dose.
In clinical trials performed in patients with tumour-induced hypercalcaemia (TIH), the overall safety profile amongst all three treatment groups (Indaferil 4 and 8 mg and pamidronate 90 mg) was similar in types and severity.
Paediatric population
Clinical trial results in the treatment of severe osteogenesis imperfecta in paediatric patients aged 1 to 17 years
The effects of intravenous Indaferil in the treatment of paediatric patients (age 1 to 17 years) with severe osteogenesis imperfecta (types I, III and IV) were compared to intravenous pamidronate in one international, multicentre, randomised, open-label study with 74 and 76 patients in each treatment group, respectively. The study treatment period was 12 months preceded by a 4- to 9-week screening period during which vitamin D and elemental calcium supplements were taken for at least 2 weeks. In the clinical programme patients aged 1 to < 3 years received 0.025 mg/kg Indaferil (up to a maximum single dose of 0.35 mg) every 3 months and patients aged 3 to 17 years received 0.05 mg/kg Indaferil (up to a maximum single dose of 0.83 mg) every 3 months. An extension study was conducted in order to examine the long-term general and renal safety of once yearly or twice yearly Indaferil over the 12-month extension treatment period in children who had completed one year of treatment with either Indaferil or pamidronate in the core study.
The primary endpoint of the study was the percent change from baseline in lumbar spine bone mineral density (BMD) after 12 months of treatment. Estimated treatment effects on BMD were similar, but the trial design was not sufficiently robust to establish non-inferior efficacy for Indaferil. In particular there was no clear evidence of efficacy on incidence of fracture or on pain. Fracture adverse events of long bones in the lower extremities were reported in approximately 24% (femur) and 14% (tibia) of Indaferil-treated patients vs 12% and 5% of pamidronate-treated patients with severe osteogenesis imperfecta, regardless of disease type and causality but overall incidence of fractures was comparable for the Indaferil and pamidronate-treated patients: 43% (32/74) vs 41% (31/76).
Interpretation of the risk of fracture is confounded by the fact that fractures are common events in patients with severe osteogenesis imperfecta as part of the disease process.
The type of adverse reactions observed in this population were similar to those previously seen in adults with advanced malignancies involving the bone. The adverse reactions ranked under headings of frequency, are presented in Table 6. The following conventional classification is used: very common (>1/10), common (>1/100, <1/10), uncommon (>1/1,000, <1/100), rare (>1/10,000, <1/1,000), very rare (<1/10,000), not known (cannot be estimated from the available data).
Table 6: Adverse reactions observed in paediatric patients with severe osteogenesis imperfecta1
| Nervous system disorders |
|
| Common: | Headache |
| Cardiac disorders |
|
| Common: | Tachycardia |
| Respiratory, thoracic and mediastinal disorders |
|
| Common: | Nasopharyngitis |
| Gastrointestinal disorders |
|
| Very common: | Vomiting, nausea |
| Common: | Abdominal pain |
| Musculoskeletal and connective tissue disorders |
|
| Common: | Pain in extremities, arthralgia, musculoskeletal pain |
| General disorders and administration site conditions | |
| Very common: | Pyrexia, fatigue |
| Common: | Acute phase reaction, pain |
| Investigations |
|
| Very common: | Hypocalcaemia |
| Common: | Hypophosphataemia |
1Adverse events occurring with frequencies < 5% were medically assessed and it was shown that these cases are consistent with the well established safety profile of Indaferil
In paediatric patients with severe osteogenesis imperfecta, Indaferil seems to be associated with more pronounced risks for acute phase reaction, hypocalcaemia and unexplained tachycardia, in comparison to pamidronate, but this difference declined after subsequent infusions.
Single and multiple 5- and 15-minute infusions of 2, 4, 8 and 16 mg zoledronic acid in 64 patients with bone metastases yielded the following pharmacokinetic data, which were found to be dose independent.
After initiating the infusion of zoledronic acid, the plasma concentrations of zoledronic acid rapidly increased, achieving their peak at the end of the infusion period, followed by a rapid decline to < 10% of peak after 4 hours and < 1% of peak after 24 hours, with a subsequent prolonged period of very low concentrations not exceeding 0.1% of peak prior to the second infusion of zoledronic acid on day 28.
Intravenously administered zoledronic acid is eliminated by a triphasic process: rapid biphasic disappearance from the systemic circulation, with half-lives of t½α 0.24 and t½β 1.87 hours, followed by a long elimination phase with a terminal elimination half-life of t½γ 146 hours. There was no accumulation of zoledronic acid in plasma after multiple doses given every 28 days. Zoledronic acid is not metabolised and is excreted unchanged via the kidney. Over the first 24 hours, 39 ± 16% of the administered dose is recovered in the urine, while the remainder is principally bound to bone tissue. From the bone tissue it is released very slowly back into the systemic circulation and eliminated via the kidney. The total body clearance is 5.04 ± 2.5 l/h, independent of dose, and unaffected by gender, age, race, and body weight. Increasing the infusion time from 5 to 15 minutes caused a 30% decrease in zoledronic acid concentration at the end of the infusion, but had no effect on the area under the plasma concentration versus time curve.
The interpatient variability in pharmacokinetic parameters for zoledronic acid was high, as seen with other bisphosphonates.
No pharmacokinetic data for zoledronic acid are available in patients with hypercalcaemia or in patients with hepatic insufficiency. Zoledronic acid does not inhibit human P450 enzymes in vitro, shows no biotransformation and in animal studies < 3% of the administered dose was recovered in the faeces, suggesting no relevant role of liver function in the pharmacokinetics of zoledronic acid.
The renal clearance of zoledronic acid was correlated with creatinine clearance, renal clearance representing 75 ± 33% of the creatinine clearance, which showed a mean of 84 ± 29 ml/min (range 22 to 143 ml/min) in the 64 cancer patients studied. Population analysis showed that for a patient with creatinine clearance of 20 ml/min (severe renal impairment), or 50 ml/min (moderate impairment), the corresponding predicted clearance of zoledronic acid would be 37% or 72%, respectively, of that of a patient showing creatinine clearance of 84 ml/min. Only limited pharmacokinetic data are available in patients with severe renal insufficiency (creatinine clearance < 30 ml/min).
In an in vitro study, zoledronic acid showed low affinity for the cellular components of human blood, with a mean blood to plasma concentration ratio of 0.59 in a concentration range of 30 ng/ml to 5000 ng/ml. The plasma protein binding is low, with the unbound fraction ranging from 60% at 2 ng/ml to 77% at 2000 ng/ml of zoledronic acid.
Special populations
Paediatric patients
Limited pharmacokinetic data in children with severe osteogenesis imperfecta suggest that zoledronic acid pharmacokinetics in children aged 3 to 17 years are similar to those in adults at a similar mg/kg dose level. Age, body weight, gender and creatinine clearance appear to have no effect on zoledronic acid systemic exposure.
Single and multiple 5- and 15-minute infusions of 2, 4, 8 and 16 mg Indaferil in 64 patients with bone metastases yielded the following pharmacokinetic data, which were found to be dose independent.
After initiating the infusion of Indaferil, the plasma concentrations of drug rapidly increased, achieving their peak at the end of the infusion period, followed by a rapid decline to < 10% of peak after 4 hours and < 1% of peak after 24 hours, with a subsequent prolonged period of very low concentrations not exceeding 0.1% of peak prior to the second infusion of drug on day 28.
Intravenously administered Indaferil is eliminated by a triphasic process: rapid biphasic disappearance from the systemic circulation, with half-lives of t½α 0.24 and t½β 1.87 hours, followed by a long elimination phase with a terminal elimination half-life of t½γ 146 hours. There was no accumulation of drug in plasma after multiple doses of the drug given every 28 days. Indaferil is not metabolised and is excreted unchanged via the kidney. Over the first 24 hours, 39 ± 16% of the administered dose is recovered in the urine, while the remainder is principally bound to bone tissue.
From the bone tissue it is released very slowly back into the systemic circulation and eliminated via the kidney. The total body clearance is 5.04 ± 2.5 l/h, independent of dose, and unaffected by gender, age, race, and body weight. Increasing the infusion time from 5 to 15 minutes caused a 30% decrease in Indaferil concentration at the end of the infusion, but had no effect on the area under the plasma concentration versus time curve.
The interpatient variability in pharmacokinetic parameters for Indaferil was high, as seen with other bisphosphonates.
No pharmacokinetic data for Indaferil are available in patients with hypercalcaemia or in patients with hepatic insufficiency. Indaferil does not inhibit human P450 enzymes in vitro, shows no biotransformation and in animal studies < 3% of the administered dose was recovered in the faeces, suggesting no relevant role of liver function in the pharmacokinetics of Indaferil.
The renal clearance of Indaferil was correlated with creatinine clearance, renal clearance representing 75 ± 33% of the creatinine clearance, which showed a mean of 84 ± 29 ml/min (range 22 to 143 ml/min) in the 64 cancer patients studied. Population analysis showed that for a patient with creatinine clearance of 20 ml/min (severe renal impairment), or 50 ml/min (moderate impairment), the corresponding predicted clearance of Indaferil would be 37% or 72%, respectively, of that of a patient showing creatinine clearance of 84 ml/min. Only limited pharmacokinetic data are available in patients with severe renal insufficiency (creatinine clearance < 30 ml/min).
In an in vitro study, Indaferil showed low affinity for the cellular components of human blood, with a mean blood to plasma concentration ratio of 0.59 in a concentration range of 30ng/ml to 5000ng/ml. The plasma protein binding is low, with the unbound fraction ranging from 60% at 2ng/ml to 77% at 2000ng/ml of Indaferil.
Special populations
Paediatric patients
Limited pharmacokinetic data in children with severe osteogenesis imperfecta suggest that Indaferil pharmacokinetics in children aged 3 to 17 years are similar to those in adults at a similar mg/kg dose level. Age, body weight, gender and creatinine clearance appear to have no effect on Indaferil systemic exposure.
General
Patients must be assessed prior to administration of Indaferil to ensure that they are adequately hydrated.
Overhydration should be avoided in patients at risk of cardiac failure.
Standard hypercalcaemia-related metabolic parameters, such as serum levels of calcium, phosphate and magnesium, should be carefully monitored after initiating Indaferil therapy. If hypocalcaemia, hypophosphataemia, or hypomagnesaemia occurs, short-term supplemental therapy may be necessary. Untreated hypercalcaemia patients generally have some degree of renal function impairment, therefore careful renal function monitoring should be considered.
Indaferil contains the same active substance as found in Aclasta (zoledronic acid). Patients being treated with Indaferil should not be treated with Aclasta or any other bisphosphonate concomitantly, since the combined effects of these agents are unknown.
Renal insufficiency
Patients with TIH and evidence of deterioration in renal function should be appropriately evaluated with consideration given as to whether the potential benefit of treatment with Indaferil outweighs the possible risk.
The decision to treat patients with bone metastases for the prevention of skeletal related events should consider that the onset of treatment effect is 2-3 months.
Indaferil has been associated with reports of renal dysfunction. Factors that may increase the potential for deterioration in renal function include dehydration, pre-existing renal impairment, multiple cycles of Indaferil and other bisphosphonates as well as use of other nephrotoxic medicinal products. While the risk is reduced with a dose of 4 mg zoledronic acid administered over 15 minutes, deterioration in renal function may still occur. Renal deterioration, progression to renal failure and dialysis have been reported in patients after the initial dose or a single dose of 4 mg zoledronic acid. Increases in serum creatinine also occur in some patients with chronic administration of Indaferil at recommended doses for prevention of skeletal related events, although less frequently.
Patients should have their serum creatinine levels assessed prior to each dose of Indaferil. Upon initiation of treatment in patients with bone metastases with mild to moderate renal impairment, lower doses of zoledronic acid are recommended. In patients who show evidence of renal deterioration during treatment, Indaferil should be withheld. Indaferil should only be resumed when serum creatinine returns to within 10% of baseline. Indaferil treatment should be resumed at the same dose as that given prior to treatment interruption.
In view of the potential impact of zoledronic acid on renal function, the lack of clinical safety data in patients with severe renal impairment (in clinical trials defined as serum creatinine > 400 µmol/l or > 4.5 mg/dl for patients with TIH and > 265 µmol/l or > 3.0 mg/dl for patients with cancer and bone metastases, respectively) at baseline and only limited pharmacokinetic data in patients with severe renal impairment at baseline (creatinine clearance < 30 ml/min), the use of Indaferil is not recommended in patients with severe renal impairment.
Hepatic insufficiency
As only limited clinical data are available in patients with severe hepatic insufficiency, no specific recommendations can be given for this patient population.
Osteonecrosis
Osteonecrosis of the jaw
Osteonecrosis of the jaw (ONJ) has been reported uncommonly in clinical trials and in the post- marketing setting in patients receiving Indaferil.
The start of treatment or of a new course of treatment should be delayed in patients with unhealed open soft tissue lesions in the mouth, except in medical emergency situations. A dental examination with appropriate preventive dentistry and an individual benefit-risk assessment is recommended prior to treatment with bisphosphonates in patients with concomitant risk factors.
The following risk factors should be considered when evaluating an individual's risk of developing ONJ:
- Potency of the bisphosphonate (higher risk for highly potent compounds), route of administration (higher risk for parenteral administration) and cumulative dose of bisphosphonate.
- Cancer, co-morbid conditions (e.g. anaemia, coagulopathies, infection), smoking.
- Concomitant therapies: chemotherapy, angiogenesis inhibitors , radiotherapy to neck and head, corticosteroids.
- History of dental disease, poor oral hygiene, periodontal disease, invasive dental procedures (e.g. tooth extractions) and poorly fitting dentures.
All patients should be encouraged to maintain good oral hygiene, undergo routine dental check-ups, and immediately report any oral symptoms such as dental mobility, pain or swelling, or non-healing of sores or discharge during treatment with Indaferil.
While on treatment, invasive dental procedures should be performed only after careful consideration and be avoided in close proximity to zoledronic acid administration. For patients who develop osteonecrosis of the jaw while on bisphosphonate therapy, dental surgery may exacerbate the condition. For patients requiring dental procedures, there are no data available to suggest whether discontinuation of bisphosphonate treatment reduces the risk of osteonecrosis of the jaw.
The management plan for patients who develop ONJ should be set up in close collaboration between the treating physician and a dentist or oral surgeon with expertise in ONJ. Temporary interruption of zoledronic acid treatment should be considered until the condition resolves and contributing risk factors are mitigated where possible.
Osteonecrosis of other anatomical sites
Osteonecrosis of the external auditory canal has been reported with bisphosphonates, mainly in association with long-term therapy. Possible risk factors for osteonecrosis of the external auditory canal include steroid use and chemotherapy and/or local risk factors such as infection or trauma. The possibility of osteonecrosis of the external auditory canal should be considered in patients receiving bisphosphonates who present with ear symptoms including chronic ear infections.
Additionally, there have been sporadic reports of osteonecrosis of other sites, including the hip and femur, reported predominantly in adult cancer patients treated with Indaferil.
Musculoskeletal pain
In post-marketing experience, severe and occasionally incapacitating bone, joint, and/or muscle pain have been reported in patients taking Indaferil. However, such reports have been infrequent. The time to onset of symptoms varied from one day to several months after starting treatment. Most patients had relief of symptoms after stopping treatment. A subset had recurrence of symptoms when rechallenged with Indaferil or another bisphosphonate.
Atypical fractures of the femur
Atypical subtrochanteric and diaphyseal femoral fractures have been reported with bisphosphonate therapy, primarily in patients receiving long-term treatment for osteoporosis. These transverse or short oblique fractures can occur anywhere along the femur from just below the lesser trochanter to just above the supracondylar flare. These fractures occur after minimal or no trauma and some patients experience thigh or groin pain, often associated with imaging features of stress fractures, weeks to months before presenting with a completed femoral fracture. Fractures are often bilateral; therefore the contralateral femur should be examined in bisphosphonate-treated patients who have sustained a femoral shaft fracture. Poor healing of these fractures has also been reported. Discontinuation of bisphosphonate therapy in patients suspected to have an atypical femur fracture should be considered pending evaluation of the patient, based on an individual benefit risk assessment.
During bisphosphonate treatment patients should be advised to report any thigh, hip or groin pain and any patient presenting with such symptoms should be evaluated for an incomplete femur fracture.
Hypocalcaemia
Hypocalcaemia has been reported in patients treated with Indaferil. Cardiac arrhythmias and neurologic adverse events (including convulsions, hypoaesthesia and tetany) have been reported secondary to cases of severe hypocalcaemia. Cases of severe hypocalcaemia requiring hospitalisation have been reported. In some instances, the hypocalcaemia may be life-threatening. Caution is advised when Indaferil is administered with medicinal products known to cause hypocalcaemia, as they may have a synergistic effect resulting in severe hypocalcaemia. Serum calcium should be measured and hypocalcaemia must be corrected before initiating Indaferil therapy. Patients should be adequately supplemented with calcium and vitamin D.
General
Patients must be assessed prior to administration of Indaferil to ensure that they are adequately hydrated.
Overhydration should be avoided in patients at risk of cardiac failure.
Standard hypercalcaemia-related metabolic parameters, such as serum levels of calcium, phosphate and magnesium, should be carefully monitored after initiating Indaferil therapy. If hypocalcaemia, hypophosphataemia, or hypomagnesaemia occurs, short-term supplemental therapy may be necessary.
Untreated hypercalcaemia patients generally have some degree of renal function impairment, therefore careful renal function monitoring should be considered.
Indaferil contains the same active substance as found in Zometa and Aclasta (Indaferil). Patients being treated with Indaferil should not be treated with Zometa or Aclasta or any other bisphosphonates concomitantly, since the combined effects of these agents are unknown.
Renal insufficiency
Patients with TIH with evidence of deterioration in renal function should be appropriately evaluated with consideration given as to whether the potential benefit of treatment with Indaferil outweighs the possible risk.
The decision to treat patients with bone metastases for the prevention of skeletal related events should consider that the onset of treatment effect is 2-3 months.
Indaferil has been associated with reports of renal dysfunction. Factors that may increase the potential for deterioration in renal function include dehydration, pre-existing renal impairment, multiple cycles of Indaferil and other bisphosphonates as well as use of other nephrotoxic medicinal products. While the risk is reduced with a dose of 4 mg Indaferil administered over 15 minutes, deterioration in renal function may still occur. Renal deterioration, progression to renal failure and dialysis have been reported in patients after the initial dose or a single dose of 4 mg Indaferil.
Increases in serum creatinine also occur in some patients with chronic administration of Indaferil at recommended doses for prevention of skeletal related events, although less frequently.
Patients should have their serum creatinine levels assessed prior to each dose of Indaferil. Upon initiation of treatment in patients with bone metastases with mild to moderate renal impairment, lower doses of Indaferil are recommended. In patients who show evidence of renal deterioration during treatment, Indaferil should be withheld. Indaferil should only be resumed when serum creatinine returns to within 10% of baseline. Indaferil treatment should be resumed at the same dose as that given prior to treatment interruption.
In view of the potential impact of Indaferil on renal function, the lack of clinical safety data in patients with severe renal impairment (in clinical trials defined as serum creatinine > 400 μmol/l or > 4.5 mg/dl for patients with TIH and > 265 μmol/l or > 3.0 mg/dl for patients with cancer and bone metastases, respectively) at baseline and only limited pharmacokinetic data in patients with severe renal impairment at baseline (creatinine clearance < 30 ml/min), the use of Indaferil is not recommended in patients with severe renal impairment.
Hepatic insufficiency
As only limited clinical data are available in patients with severe hepatic insufficiency, no specific recommendations can be given for this patient population.
Osteonecrosis
Osteonecrosis of the jaw
Osteonecrosis of the jaw (ONJ) has been reported uncommonly in clinical trials and in the post marketing setting in patients receiving Indaferil.
The start of treatment or of a new course of treatment should be delayed in patients with unhealed open soft tissue lesions in the mouth, except in medical emergency situations. A dental examination with appropriate preventive dentistry and an individual benefit-risk assessment is recommended prior to treatment with bisphosphonates in patients with concomitant risk factors.
The following risk factors should be considered when evaluating an individual's risk of developing ONJ:
- Potency of the bisphosphonate (higher risk for highly potent compounds), route of administration (higher risk for parenteral administration) and cumulative dose of bisphosphonates.
- Cancer, co-morbid conditions (e.g. anaemia, coagulopathies, infection), smoking.
- Concomitant therapies: chemotherapy, angiogenesis inhibitors , radiotherapy to neck and head, corticosteroids.
- History of dental disease, poor oral hygiene, periodontal disease, invasive dental procedures (e.g. tooth extractions) and poorly fitting dentures
All patients should be encouraged to maintain good oral hygiene, undergo routine dental check-ups, and immediately report any oral symptoms such as dental mobility, pain or swelling, or non-healing of sores or discharge during treatment with Indaferil.
While on treatment, invasive dental procedures should be performed only after careful consideration and be avoided in close proximity to Indaferil administration. For patients who develop osteonecrosis of the jaw while on bisphosphonate therapy, dental surgery may exacerbate the condition. For patients requiring dental procedures, there are no data available to suggest whether discontinuation of bisphosphonate treatment reduces the risk of osteonecrosis of the jaw.
The management plan for patients who develop ONJ should be set up in close collaboration between the treating physician and a dentist or oral surgeon with expertise in ONJ. Temporary interruption of Indaferil treatment should be considered until the condition resolves and contributing risk factors are mitigated where possible.
Osteonecrosis of other anatomical sites
Osteonecrosis of the external auditory canal has been reported with bisphosphonates, mainly in association with long-term therapy. Possible risk factors for osteonecrosis of the external auditory canal include steroid use and chemotherapy and/or local risk factors such as infection or trauma. The possibility of osteonecrosis of the external auditory canal should be considered in patients receiving bisphosphonates who present with ear symptoms including chronic ear infections.
Additionally, there have been sporadic reports of osteonecrosis of other sites, including the hip and femur, reported predominantly in adult cancer patients treated with Indaferil.
Musculoskeletal pain
In post-marketing experience, severe and occasionally incapacitating bone, joint, and/or muscle pain have been reported in patients taking Indaferil. However, such reports have been infrequent.
The time to onset of symptoms varied from one day to several months after starting treatment. Most patients had relief of symptoms after stopping treatment. A subset had recurrence of symptoms when rechallenged with Indaferil or another bisphosphonate.
Atypical fractures of the femur
Atypical subtrochanteric and diaphyseal femoral fractures have been reported with bisphosphonate therapy, primarily in patients receiving long-term treatment for osteoporosis. These transverse or short oblique fractures can occur anywhere along the femur from just below the lesser trochanter to just above the supracondylar flare. These fractures occur after minimal or no trauma and some patients experience thigh or groin pain, often associated with imaging features of stress fractures, weeks to months before presenting with a completed femoral fracture. Fractures are often bilateral; therefore the contralateral femur should be examined in bisphosphonate-treated patients who have sustained a femoral shaft fracture. Poor healing of these fractures has also been reported. Discontinuation of bisphosphonate therapy in patients suspected to have an atypical femur fracture should be considered pending evaluation of the patient, based on an individual benefit risk assessment.
During bisphosphonate treatment patients should be advised to report any thigh, hip or groin pain and any patient presenting with such symptoms should be evaluated for an incomplete femur fracture.
Hypocalcaemia
Hypocalcaemia has been reported in patients treated with Indaferil. Cardiac arrhythmias and neurologic adverse events (including convulsions, hypoaesthesia and tetany) have been reported secondary to cases of severe hypocalcaemia. Cases of severe hypocalcaemia requiring hospitalisation have been reported. In some instances, the hypocalcaemia may be life-threatening. Caution is advised when Indaferil is administered with medicinal products known to cause hypocalcaemia, as they may have a synergistic effect resulting in severe hypocalcaemia. Serum calcium should be measured and hypocalcaemia must be corrected before initiating therapy with Indaferil. Patients should be adequately supplemented with calcium and vitamin D.
Adverse reactions, such as dizziness and somnolence, may have influence on the ability to drive or use machines, therefore caution should be exercised with the use of Indaferil along with driving and operating of machinery.
Indaferil must only be prescribed and administered to patients by healthcare professionals experienced in the administration of intravenous bisphosphonates. Patients treated with Indaferil should be given the package leaflet and the patient reminder card.
Posology
Prevention of skeletal related events in patients with advanced malignancies involving bone
Adults and older people
The recommended dose in the prevention of skeletal related events in patients with advanced malignancies involving bone is 4 mg zoledronic acid every 3 to 4 weeks.
Patients should also be administered an oral calcium supplement of 500 mg and 400 IU vitamin D daily.
The decision to treat patients with bone metastases for the prevention of skeletal related events should consider that the onset of treatment effect is 2-3 months.
Treatment of TIH
Adults and older people
The recommended dose in hypercalcaemia (albumin-corrected serum calcium > 12.0 mg/dl or 3.0 mmol/l) is a single dose of 4 mg zoledronic acid.
Renal impairment
TIH:
Indaferil treatment in TIH patients who also have severe renal impairment should be considered only after evaluating the risks and benefits of treatment. In the clinical studies, patients with serum creatinine > 400 µmol/l or > 4.5 mg/dl were excluded. No dose adjustment is necessary in TIH patients with serum creatinine < 400 µmol/l or < 4.5 mg/dl.
Prevention of skeletal related events in patients with advanced malignancies involving bone:
When initiating treatment with Indaferil in patients with multiple myeloma or metastatic bone lesions from solid tumours, serum creatinine and creatinine clearance (CLcr) should be determined. CLcr is calculated from serum creatinine using the Cockcroft-Gault formula. Indaferil is not recommended for patients presenting with severe renal impairment prior to initiation of therapy, which is defined for this population as CLcr < 30 ml/min. In clinical trials with Indaferil, patients with serum creatinine > 265 µmol/l or > 3.0 mg/dl were excluded.
For patients with normal renal function (defined as CLcr > 60 ml/min), zoledronic acid 4 mg/100 ml solution for infusion may be administered directly without any further preparation.).
| Baseline creatinine clearance (ml/min) | Indaferil recommended dose* |
| > 60 | 4.0 mg zoledronic acid |
| 50-60 | 3.5 mg* zoledronic acid |
| 40-49 | 3.3 mg* zoledronic acid |
| 30-39 | 3.0 mg* zoledronic acid |
* Doses have been calculated assuming target AUC of 0.66 (mg-hr/l) (CLcr = 75 ml/min). The reduced doses for patients with renal impairment are expected to achieve the same AUC as that seen in patients with creatinine clearance of 75 ml/min.
Following initiation of therapy, serum creatinine should be measured prior to each dose of Indaferil and treatment should be withheld if renal function has deteriorated. In the clinical trials, renal deterioration was defined as follows:
- For patients with normal baseline serum creatinine (< 1.4 mg/dl or < 124 µmol/l), an increase of 0.5 mg/dl or 44 µmol/l;
- For patients with abnormal baseline creatinine (> 1.4 mg/dl or > 124 µmol/l), an increase of 1.0 mg/dl or 88 µmol/l.
In the clinical studies, Indaferil treatment was resumed only when the creatinine level returned to within 10% of the baseline value. Indaferil treatment should be resumed at the same dose as that given prior to treatment interruption.
Paediatric population
The safety and efficacy of zoledronic acid in children aged 1 year to 17 years have not been established. Currently available data are described in section and 5.1 but no recommendation on a posology can be made.
Method of administration
Intravenous use.
Indaferil 4 mg/100 ml solution for infusion should be given as a single intravenous infusion in no less than 15 minutes.
In patients with normal renal function, defined as CLcr > 60 ml/min, zoledronic acid 4 mg/100 ml solution for infusion must not be further diluted.
To prepare reduced doses for patients with baseline CLcr ≤ 60 ml/min, refer to Table 1 below. Remove the volume of Indaferil solution indicated from the bottle and replace with an equal volume of sterile sodium chloride 9 mg/ml (0,9%) solution for injection, or 5% glucose solution for injection.
Table 1: Preparation of reduced doses of Indaferil 4 mg/100 ml solution for infusion
| Baseline creatinine clearance (ml/min) | Remove the following amount of Indaferil solution for infusion (ml) | Replace with the following volume of sterile sodium chloride 9 mg/ml (0,9%), or 5% glucose solution for injection (ml) | Adjusted dose (mg zoledronic acid in 100 ml) |
| 50-60 | 12.0 | 12.0 | 3.5 |
| 40-49 | 18.0 | 18.0 | 3.3 |
| 30-39 | 25.0 | 25.0 | 3.0 |
Indaferil 4 mg/100 ml solution for infusion must not be mixed with other infusion solutions and should be administered as a single intravenous solution in a separate infusion line.
Patients must be maintained well hydrated prior to and following administration of Indaferil.
Indaferil must only be prescribed and administered to patients by healthcare professionals experienced in the administration of intravenous bisphosphonates. Patients treated with Indaferil should be given the package leaflet and the patient reminder card.
Posology
Prevention of skeletal related events in patients with advanced malignancies involving bone
Adults and older people
The recommended dose in the prevention of skeletal related events in patients with advanced malignancies involving bone is 4 mg Indaferil every 3 to 4 weeks.
Patients should also be administered an oral calcium supplement of 500 mg and 400 IU vitamin D daily.
The decision to treat patients with bone metastases for the prevention of skeletal related events should consider that the onset of treatment effect is 2-3 months.
Treatment of TIH
Adults and older people
The recommended dose in hypercalcaemia (albumin-corrected serum calcium > 12.0 mg/dl or 3.0 mmol/l) is a single dose of 4 mg Indaferil.
Renal impairment
TIH:
Indaferil treatment in TIH patients who also have severe renal impairment should be considered only after evaluating the risks and benefits of treatment. In the clinical studies, patients with serum creatinine > 400 μmol/l or > 4.5 mg/dl were excluded. No dose adjustment is necessary in TIH patients with serum creatinine < 400 μmol/l or < 4.5 mg/dl.
Prevention of skeletal related events in patients with advanced malignancies involving bone:
When initiating treatment with Indaferil in patients with multiple myeloma or metastatic bone lesions from solid tumours, serum creatinine and creatinine clearance (CLcr) should be determined. CLcr is calculated from serum creatinine using the Cockcroft-Gault formula. Indaferil is not recommended for patients presenting with severe renal impairment prior to initiation of therapy, which is defined for this population as CLcr < 30 ml/min. In clinical trials with Indaferil, patients with serum creatinine > 265 μmol/l or > 3.0 mg/dl were excluded.
| Baseline Creatinine Clearance (ml/min) | Indaferil Recommended Dose* |
| > 60 50-60 40-49 30-39 | 4.0 mg Indaferil 3.5 mg* Indaferil 3.3 mg* Indaferil 3.0 mg* Indaferil |
*Doses have been calculated assuming target AUC of 0.66 (mg-hr/l) (CLcr=75 ml/min). The reduced doses for patients with renal impairment are expected to achieve the same AUC as that seen in patients with creatinine clearance of 75 ml/min.
Following initiation of therapy, serum creatinine should be measured prior to each dose of Indaferil and treatment should be withheld if renal function has deteriorated. In the clinical trials, renal deterioration was defined as follows:
▪ For patients with normal baseline serum creatinine (< 1.4 mg/dl or < 124 μmol/l), an increase of 0.5 mg/dl or 44 μmol/l;
▪ For patients with an abnormal baseline creatinine (> 1.4 mg/dl or > 124 μmol/l), an increase of 1.0 mg/dl or 88 μmol/l.
In the clinical studies, Indaferil treatment was resumed only when the creatinine level returned to within 10% of the baseline value. Indaferil treatment should be resumed at the same dose as that given prior to treatment interruption.
Paediatric population
The safety and efficacy of Indaferil in children aged 1 year to 17 years have not been established.1 but no recommendation on a posology can be made.
Method of administration
Intravenous use.
Indaferil 4 mg/5 ml concentrate for solution for infusion, further diluted in 100 ml , should be given as a single intravenous infusion in no less than 15 minutes.
Instructions for preparing reduced doses of Indaferil
Withdraw an appropriate volume of the concentrate needed, as follows:
- 4.4 ml for 3.5 mg dose
- 4.1 ml for 3.3 mg dose
- 3.8 ml for 3.0 mg dose
The withdrawn amount of concentrate must be further diluted in 100 ml of sterile 0.9% w/v sodium chloride solution or 5% w/v glucose solution. The dose must be given as a single intravenous infusion over no less than 15 minutes.Indaferil concentrate must not be mixed with calcium or other divalent cation-containing infusion solutions such as lactated Ringer's solution, and should be administered as a single intravenous solution in a separate infusion line.
Patients must be maintained well hydrated prior to and following administration of Indaferil.
Aseptic techniques must be followed during the preparation of the infusion. For single use only.
Only clear solution free from particles and discolouration should be used.
Healthcare professionals are advised not to dispose of unused Indaferil via the domestic sewage system.
Any unused medicinal product or waste material should be disposed of in accordance with local requirements.
Prior to administration, 5.0 ml concentrate from one vial or the volume of the concentrate withdrawn as required must be further diluted with 100 ml of calcium-free infusion solution (0.9% w/v sodium chloride solution or 5% w/v glucose solution).
Aseptic techniques must be followed during the preparation of the infusion.
For single use only.
Only clear solution free from particles and discolouration should be used.
Healthcare professionals are advised not to dispose of unused Indaferil via the domestic sewage system.
Any unused medicinal product or waste material should be disposed of in accordance with local requirements.
