Generic Name: caspofungin acetate
Dosage Form: injection, powder, lyophilized, for solution
Indications and Usage for Cancidas
Empirical Therapy for Presumed Fungal Infections in Febrile, Neutropenic Patients
Treatment of Candidemia and Other Candida Infections
Cancidas is indicated for the treatment of candidemia and the following candida infections: intra-abdominal abscesses, peritonitis, and pleural space infections in adult and pediatric patients (3 months of age and older) [see Clinical Studies (14.2, 14.5)].
Limitation of Use: Cancidas has not been studied in endocarditis, osteomyelitis, and meningitis due to Candida.
Treatment of Esophageal Candidiasis
Limitation of Use: Cancidas has not been approved for the treatment of oropharyngeal candidiasis (OPC). In the study that evaluated the efficacy of caspofungin in the treatment of esophageal candidiasis, patients with concomitant OPC had higher relapse rate of the OPC [see Clinical Studies (14.3)].
Treatment of Invasive Aspergillosis in Patients Who Are Refractory to or Intolerant of Other Therapies
Cancidas is indicated for the treatment of invasive aspergillosis in adult and pediatric patients (3 months of age and older) who are refractory to or intolerant of other therapies [see Clinical Studies (14.4, 14.5)].
Limitation of Use: Cancidas has not been studied as initial therapy for invasive aspergillosis.
Cancidas Dosage and Administration
Important Administration Instructions for Use in All Patients
Administer Cancidas by slow intravenous (IV) infusion over approximately 1 hour. Do not administer Cancidas by IV bolus administration.
Recommended Dosage in Adult Patients [18 years of age and older]
The dosage and duration of Cancidas treatment for each indication are as follows:
Empirical Therapy for Presumed Fungal Infections in Febrile Neutropenic Patients
Administer a single 70-mg loading dose on Day 1, followed by 50 mg once daily thereafter. Duration of treatment should be based on the patient's clinical response. Continue empirical therapy until resolution of neutropenia. In general, treat patients found to have a fungal infection for a minimum of 14 days after the last positive culture and continue treatment for at least 7 days after both neutropenia and clinical symptoms are resolved. If the 50-mg dose is well tolerated but does not provide an adequate clinical response, the daily dose can be increased to 70 mg.
Candidemia and Other Candida Infections
Administer a single 70-mg loading dose on Day 1, followed by 50 mg once daily thereafter. Duration of treatment should be dictated by the patient's clinical and microbiological response. In general, continue antifungal therapy for at least 14 days after the last positive culture. Patients with neutropenia who remain persistently neutropenic may warrant a longer course of therapy pending resolution of the neutropenia.
The dose is 50 mg once daily for 7 to 14 days after symptom resolution. A 70-mg loading dose has not been studied for this indication. Because of the risk of relapse of oropharyngeal candidiasis in patients with HIV infections, suppressive oral therapy could be considered [see Clinical Studies (14.3)].
Administer a single 70-mg loading dose on Day 1, followed by 50 mg once daily thereafter. Duration of treatment should be based upon the severity of the patient's underlying disease, recovery from immunosuppression, and clinical response.
Recommended Dosing in Pediatric Patients [3 months to 17 years of age]
For all indications, administer a single 70 mg/m2 loading dose on Day 1, followed by 50 mg/m2 once daily thereafter. The maximum loading dose and the daily maintenance dose should not exceed 70 mg, regardless of the patient's calculated dose. Dosing in pediatric patients (3 months to 17 years of age) should be based on the patient's body surface area (BSA) as calculated by the Mosteller Formula [see References (15)]:
Following calculation of the patient's BSA, the loading dose in milligrams should be calculated as BSA (m2) × 70 mg/m2. The maintenance dose in milligrams should be calculated as BSA (m2) × 50 mg/m2.
Duration of treatment should be individualized to the indication, as described for each indication in adults [see Dosage and Administration (2.2)]. If the 50-mg/m2 daily dose is well tolerated but does not provide an adequate clinical response, the daily dose can be increased to 70 mg/m2 daily (not to exceed 70 mg).
Dosage Adjustments in Patients with Hepatic Impairment
Adult patients with mild hepatic impairment (Child-Pugh score 5 to 6) do not need a dosage adjustment. For adult patients with moderate hepatic impairment (Child-Pugh score 7 to 9), Cancidas 35 mg once daily is recommended based upon pharmacokinetic data [see Clinical Pharmacology (12.3)] with a 70-mg loading dose administered on Day 1 where appropriate. There is no clinical experience in adult patients with severe hepatic impairment (Child-Pugh score greater than 9) and in pediatric patients with any degree of hepatic impairment.
Dosage Adjustments in Patients Receiving Concomitant Inducers of Hepatic CYP Enzymes
Adult patients on rifampin should receive 70 mg of Cancidas once daily. When Cancidas is co-administered to adult patients with other inducers of hepatic CYP enzymes such as nevirapine, efavirenz, carbamazepine, dexamethasone, or phenytoin, administration of a daily dose of 70 mg of Cancidas should be considered [see Drug Interactions (7)].
Pediatric patients on rifampin should receive 70 mg/m2 of Cancidas daily (not to exceed an actual daily dose of 70 mg. When Cancidas is co-administered to pediatric patients with other inducers of hepatic CYP enzymes, such as efavirenz, nevirapine, phenytoin, dexamethasone, or carbamazepine, a Cancidas dose of 70 mg/m2 once daily (not to exceed 70 mg) should be considered [see Drug Interactions (7)].
Preparation for Administration
Reconstitution of Cancidas for Intravenous Infusion
- Equilibrate the refrigerated vial of Cancidas to room temperature.
- Aseptically add 10.8 mL of 0.9% Sodium Chloride Injection, Sterile Water for Injection, Bacteriostatic Water for Injection with methylparaben and propylparaben, or Bacteriostatic Water for Injection with 0.9% benzyl alcohol to the vial.
- Each vial of Cancidas contains an intentional overfill of Cancidas. Thus, the drug concentration of the resulting solution is listed in Table 1 below.
Table 1: Information for Preparation of Cancidas Cancidas vial Total Drug Content
Reconstitution Volume to be added Resulting Concentration following Reconstitution 50 mg 54.6 mg 10.8 mL 5 mg/mL 70 mg 75.6 mg 10.8 mL 7 mg/mL
- The white to off-white cake will dissolve completely. Mix gently until a clear solution is obtained. Visually inspect the reconstituted solution for particulate matter or discoloration during reconstitution and prior to infusion. Do not use if the solution is cloudy or has precipitated.
- The reconstituted solution of Cancidas in the vial may be stored for up to one hour at ≤25°C (≤77°F) prior to the preparation of the infusion solution in the intravenous bag or bottle.
- Cancidas vials are for single use only. Discard unused portion.
Dilution of the Reconstituted Solution in the Intravenous Bag for Infusion
- Aseptically transfer the appropriate volume (mL) of reconstituted Cancidas to an intravenous (IV) bag (or bottle) containing 250 mL of 0.9%, 0.45%, or 0.225% Sodium Chloride Injection or Lactated Ringers Injection.
- Alternatively, the volume (mL) of reconstituted Cancidas can be added to a reduced volume of 0.9%, 0.45%, or 0.225% Sodium Chloride Injection or Lactated Ringers Injection, not to exceed a final concentration of 0.5 mg/mL.
- This diluted infusion solution in the intravenous bag or bottle must be used within 24 hours if stored at ≤25°C (≤77°F) or within 48 hours if stored refrigerated at 2 to 8°C (36 to 46°F).
Important Reconstitution and Dilution Instructions for Pediatric Patients 3 Months of Age and Older
Follow the reconstitution procedures described above using either the 70-mg or 50-mg vial to create the reconstituted solution [see Dosage and Administration (2.3)]. From the reconstituted solution in the vial, remove the volume of drug equal to the calculated loading dose or calculated maintenance dose based on a concentration of 7 mg/mL (if reconstituted from the 70-mg vial) or a concentration of 5 mg/mL (if reconstituted from the 50-mg vial).
The choice of vial should be based on total milligram dose of drug to be administered to the pediatric patient. To help ensure accurate dosing, it is recommended for pediatric doses less than 50 mg that 50-mg vials (with a concentration of 5 mg/mL) be used if available. The 70-mg vial should be reserved for pediatric patients requiring doses greater than 50 mg.
The maximum loading dose and the daily maintenance dose should not exceed 70 mg, regardless of the patient's calculated dose.
Do not mix or co-infuse Cancidas with other medications, as there are no data available on the compatibility of Cancidas with other intravenous substances, additives, or medications.
Do not use diluents containing dextrose (α-D-glucose), as Cancidas is not stable in diluents containing dextrose.
Dosage Forms and Strengths
Cancidas 50 mg is a white to off-white lyophilized cake or powder for reconstitution in a single-dose glass vial with a red aluminum band and a plastic cap. Cancidas 50-mg vial contains 54.6 mg of caspofungin.
Cancidas 70 mg is a white to off-white lyophilized cake or powder for reconstitution in a single-dose glass vial with a yellow/orange aluminum band and a plastic cap. Cancidas 70-mg vial contains 75.6 mg of caspofungin.
Cancidas is contraindicated in patients with known hypersensitivity (e.g., anaphylaxis) to any component of this product [see Adverse Reactions (6)].
Warnings and Precautions
Anaphylaxis and other hypersensitivity reactions have been reported during administration of Cancidas.
Possible histamine-mediated adverse reactions, including rash, facial swelling, angioedema, pruritus, sensation of warmth or bronchospasm have been reported.
Cases of Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN), some with a fatal outcome, have been reported with use of Cancidas [see Adverse Reactions (6.2)].
Discontinue Cancidas at the first sign or symptom of a hypersensitivity reaction and administer appropriate treatment.
Laboratory abnormalities in liver function tests have been seen in healthy volunteers and in adult and pediatric patients treated with Cancidas. In some adult and pediatric patients with serious underlying conditions who were receiving multiple concomitant medications with Cancidas, isolated cases of clinically significant hepatic dysfunction, hepatitis, and hepatic failure have been reported; a causal relationship to Cancidas has not been established. Monitor patients who develop abnormal liver function tests during Cancidas therapy for evidence of worsening hepatic function and evaluated for risk/benefit of continuing Cancidas therapy.
Elevated Liver Enzymes During Concomitant Use With Cyclosporine
Elevated liver enzymes have occurred in patients receiving Cancidas and cyclosporine concomitantly. Only use Cancidas and cyclosporine in those patients for whom the potential benefit outweighs the potential risk. Patients who develop abnormal liver enzymes during concomitant therapy should be monitored and the risk/benefit of continuing therapy should be evaluated.
The following serious adverse reactions are discussed in detail in another section of the labeling:
- Hypersensitivity [see Warnings and Precautions (5.1)]
- Hepatic Effects [see Warnings and Precautions (5.2)]
- Elevated Liver Enzymes During Concomitant Use With Cyclosporine [see Warnings and Precautions (5.3)]
Clinical Trials Experience
Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in clinical trials of Cancidas cannot be directly compared to rates in clinical trials of another drug and may not reflect the rates observed in practice.
Clinical Trials Experience in Adults
The overall safety of Cancidas was assessed in 1865 adult individuals who received single or multiple doses of Cancidas: 564 febrile, neutropenic patients (empirical therapy study); 382 patients with candidemia and/or intra-abdominal abscesses, peritonitis, or pleural space infections (including 4 patients with chronic disseminated candidiasis); 297 patients with esophageal and/or oropharyngeal candidiasis; 228 patients with invasive aspergillosis; and 394 individuals in phase I studies. In the empirical therapy study patients had undergone hematopoietic stem-cell transplantation or chemotherapy. In the studies involving patients with documented Candida infections, the majority of the patients had serious underlying medical conditions (e.g., hematologic or other malignancy, recent major surgery, HIV) requiring multiple concomitant medications. Patients in the noncomparative Aspergillus studies often had serious predisposing medical conditions (e.g., bone marrow or peripheral stem cell transplants, hematologic malignancy, solid tumors or organ transplants) requiring multiple concomitant medications.
Empirical Therapy for Presumed Fungal Infections in Febrile Neutropenic Patients
In the randomized, double-blinded empirical therapy study, patients received either Cancidas 50 mg/day (following a 70-mg loading dose) or AmBisome® (amphotericin B liposome for injection, 3 mg/kg/day). In this study clinical or laboratory hepatic adverse reactions were reported in 39% and 45% of patients in the Cancidas and AmBisome groups, respectively. Also reported was an isolated, serious adverse reaction of hyperbilirubinemia. Adverse reactions occurring in 7.5% or greater of the patients in either treatment group are presented in Table 2.
|Within any system organ class, individuals may experience more than 1 adverse reaction.|
|All Systems, Any Adverse Reaction||95||97|
|Alanine Aminotransferase Increased||18||20|
|Blood Alkaline Phosphatase Increased||15||23|
|Blood Potassium Decreased||15||23|
|Aspartate Aminotransferase Increased||14||17|
|Blood Bilirubin Increased||10||14|
|Blood Magnesium Decreased||7||9|
|Blood Glucose Increased||6||9|
|Bilirubin Conjugated Increased||5||9|
|Blood Urea Increased||4||8|
|Blood Creatinine Increased||3||11|
|General Disorders and Administration Site Conditions||57||63|
|Respiratory, Thoracic and Mediastinal Disorders||47||49|
|Skin and Subcutaneous Tissue Disorders||42||37|
|Nervous System Disorders||25||27|
|Metabolism and Nutrition Disorders||21||24|
The proportion of patients who experienced an infusion-related adverse reaction (defined as a systemic event, such as pyrexia, chills, flushing, hypotension, hypertension, tachycardia, dyspnea, tachypnea, rash, or anaphylaxis, that developed during the study therapy infusion and one hour following infusion) was significantly lower in the group treated with Cancidas (35%) than in the group treated with AmBisome (52%).
To evaluate the effect of Cancidas and AmBisome on renal function, nephrotoxicity was defined as doubling of serum creatinine relative to baseline or an increase of greater than or equal to 1 mg/dL in serum creatinine if baseline serum creatinine was above the upper limit of the normal range. Among patients whose baseline creatinine clearance was greater than 30 mL/min, the incidence of nephrotoxicity was significantly lower in the group treated with Cancidas (3%) than in the group treated with AmBisome (12%).
Candidemia and Other Candida Infections
In the randomized, double-blinded invasive candidiasis study, patients received either Cancidas 50 mg/day (following a 70-mg loading dose) or amphotericin B 0.6 to 1 mg/kg/day. Adverse reactions occurring in 10% or greater of the patients in either treatment group are presented in Table 3.
|Within any system organ class, individuals may experience more than 1 adverse reaction.|
|All Systems, Any Adverse Reaction||96||99|
|Blood Potassium Decreased||23||32|
|Blood Alkaline Phosphatase Increased||21||32|
|Alanine Aminotransferase Increased||16||15|
|Aspartate Aminotransferase Increased||16||14|
|Blood Bilirubin Increased||13||17|
|Blood Creatinine Increased||11||28|
|Red Blood Cells Urine Positive||10||10|
|Blood Urea Increased||9||23|
|Bilirubin Conjugated Increased||8||14|
|General Disorders and Administration Site Conditions||47||63|
|Respiratory, Thoracic and Mediastinal Disorders||40||54|
|Skin and Subcutaneous Tissue Disorders||25||28|
|Blood and Lymphatic System Disorders||15||13|
The proportion of patients who experienced an infusion-related adverse reaction (defined as a systemic event, such as pyrexia, chills, flushing, hypotension, hypertension, tachycardia, dyspnea, tachypnea, rash, or anaphylaxis, that developed during the study therapy infusion and one hour following infusion) was significantly lower in the group treated with Cancidas (20%) than in the group treated with amphotericin B (49%).
To evaluate the effect of Cancidas and amphotericin B on renal function, nephrotoxicity was defined as doubling of serum creatinine relative to baseline or an increase of greater than or equal to 1 mg/dL in serum creatinine if baseline serum creatinine was above the upper limit of the normal range. In a subgroup of patients whose baseline creatinine clearance was greater than 30 mL/min, the incidence of nephrotoxicity was significantly lower in the group treated with Cancidas than in the group treated with amphotericin B.
In a second randomized, double-blinded invasive candidiasis study, patients received either Cancidas 50 mg/day (following a 70-mg loading dose) or Cancidas 150 mg/day. The proportion of patients who experienced any adverse reaction was similar in the 2 treatment groups; however, this study was not large enough to detect differences in rare or unexpected adverse reactions. Adverse reactions occurring in 5% or greater of the patients in either treatment group are presented in Table 4.
|Adverse Reactions||Cancidas 50 mg†
|Cancidas 150 mg
|Within any system organ class, individuals may experience more than 1 adverse event|
|All Systems, Any Adverse Reaction||83||83|
|General Disorders and Administration Site Conditions||33||27|
|Alkaline Phosphatase Increased||12||9|
|Aspartate Aminotransferase Increased||6||9|
|Blood potassium decreased||6||8|
|Alanine Aminotransferase Increased||4||7|
Esophageal Candidiasis and Oropharyngeal Candidiasis
Adverse reactions occurring in 10% or greater of patients with esophageal and/or oropharyngeal candidiasis are presented in Table 5.
|Within any system organ class, individuals may experience more than 1 adverse reaction.|
|All Systems, Any Adverse Reaction||90||93|
|Aspartate Aminotransferase Increased||13||19|
|Blood Alkaline Phosphatase Increased||13||17|
|Alanine Aminotransferase Increased||12||17|
|White Blood Cell Count Decreased||12||19|
|General Disorders and Administration Site Conditions||31||36|
|Nervous System Disorders||18||17|
In an open-label, noncomparative aspergillosis study, in which 69 patients received Cancidas (70-mg loading dose on Day 1 followed by 50 mg daily), the following adverse reactions were observed with an incidence of 12.5% or greater: blood alkaline phosphatase increased (22%), hypotension (20%), respiratory failure (20%), pyrexia (17%), diarrhea (15%), nausea (15%), headache (15%), rash (13%), alanine aminotransferase increased (13%), aspartate aminotransferase increased (13%), blood bilirubin increased (13%), and blood potassium decreased (13%). Also reported in this patient population were pulmonary edema, ARDS (adult respiratory distress syndrome), and radiographic infiltrates.
Clinical Trials Experience in Pediatric Patients (3 months to 17 years of age)
The overall safety of Cancidas was assessed in 171 pediatric patients who received single or multiple doses of Cancidas. The distribution among the 153 pediatric patients who were over the age of 3 months was as follows: 104 febrile, neutropenic patients; 38 patients with candidemia and/or intra-abdominal abscesses, peritonitis, or pleural space infections; 1 patient with esophageal candidiasis; and 10 patients with invasive aspergillosis. The overall safety profile of Cancidas in pediatric patients is comparable to that in adult patients. Table 6 shows the incidence of adverse reactions reported in 7.5% or greater of pediatric patients in clinical studies.
One patient (0.6%) receiving Cancidas, and three patients (12%) receiving AmBisome developed a serious drug-related adverse reaction. Two patients (1%) were discontinued from Cancidas and three patients (12%) were discontinued from AmBisome due to a drug-related adverse reaction. The proportion of patients who experienced an infusion-related adverse reaction (defined as a systemic event, such as pyrexia, chills, flushing, hypotension, hypertension, tachycardia, dyspnea, tachypnea, rash, or anaphylaxis, that developed during the study therapy infusion and one hour following infusion) was 22% in the group treated with Cancidas and 35% in the group treated with AmBisome.
|Noncomparative Clinical Studies||Comparator-Controlled Clinical Study of Empirical Therapy|
|Within any system organ class, individuals may experience more than 1 adverse reaction.|
|All Systems, Any Adverse Reaction||95||96||89|
|Blood Potassium Decreased||18||9||27|
|Aspartate Aminotransferase Increased||17||2||12|
|Alanine Aminotransferase Increased||14||5||12|
|Blood Potassium Increased||3||0||8|
|General Disorders and Administration Site Conditions||47||59||42|
|Infections and Infestations||40||30||35|
|Central Line Infection||1||9||0|
|Skin and Subcutaneous Tissue Disorders||33||41||39|
|Metabolism and Nutrition Disorders||22||11||23|
|Nervous System Disorders||13||16||8|
|Musculoskeletal and Connective Tissue Disorders||11||14||12|
|Blood and Lymphatic System Disorders||10||2||15|
Overall Safety Experience of Cancidas in Clinical Trials
The overall safety of Cancidas was assessed in 2036 individuals (including 1642 adult or pediatric patients and 394 volunteers) from 34 clinical studies. These individuals received single or multiple (once daily) doses of Cancidas, ranging from 5 mg to 210 mg. Full safety data is available from 1951 individuals, as the safety data from 85 patients enrolled in 2 compassionate use studies was limited solely to serious adverse reactions. Adverse reactions which occurred in 5% or greater of all individuals who received Cancidas in these trials are shown in Table 7.
Overall, 1665 of the 1951 (85%) patients/volunteers who received Cancidas experienced an adverse reaction.
(N = 1951)
|All Systems, Any Adverse Reaction||1665||(85)|
|Alanine Aminotransferase Increased||258||(13)|
|Aspartate Aminotransferase Increased||233||(12)|
|Blood Alkaline Phosphatase Increased||232||(12)|
|Blood Potassium Decreased||220||(11)|
|Blood Bilirubin Increased||117||(6)|
|General Disorders and Administration Site Conditions||843||(43)|
|Infections and Infestations||730||(37)|
|Respiratory, Thoracic, and Mediastinal Disorders||613||(31)|
|Skin and Subcutaneous Tissue Disorders||520||(27)|
|Nervous System Disorders||412||(21)|
Clinically significant adverse reactions, regardless of causality or incidence which occurred in less than 5% of patients are listed below.
- Blood and lymphatic system disorders: anemia, coagulopathy, febrile neutropenia, neutropenia, thrombocytopenia
- Cardiac disorders: arrhythmia, atrial fibrillation, bradycardia, cardiac arrest, myocardial infarction, tachycardia
- Gastrointestinal disorders: abdominal distension, abdominal pain upper, constipation, dyspepsia
- General disorders and administration site conditions: asthenia, fatigue, infusion site pain/pruritus/swelling, mucosal inflammation, edema
- Hepatobiliary disorders: hepatic failure, hepatomegaly, hepatotoxicity, hyperbilirubinemia, jaundice
- Infections and infestations: bacteremia, sepsis, urinary tract infection
- Metabolic and nutrition disorders: anorexia, decreased appetite, fluid overload, hypomagnesemia, hypercalcemia, hyperglycemia, hypokalemia
- Musculoskeletal, connective tissue, and bone disorders: arthralgia, back pain, pain in extremity
- Nervous system disorders: convulsion, dizziness, somnolence, tremor
- Psychiatric disorders: anxiety, confusional state, depression, insomnia
- Renal and urinary disorders: hematuria, renal failure
- Respiratory, thoracic, and mediastinal disorders: dyspnea, epistaxis, hypoxia, tachypnea
- Skin and subcutaneous tissue disorders: erythema, petechiae, skin lesion, urticaria
- Vascular disorders: flushing, hypertension, phlebitis
The following additional adverse reactions have been identified during the post-approval use of Cancidas. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.
- Gastrointestinal disorders: pancreatitis
- Hepatobiliary disorders: hepatic necrosis
- Skin and subcutaneous tissue disorders: erythema multiforme, toxic epidermal necrolysis, Stevens-Johnson syndrome, and skin exfoliation
- Renal and urinary disorders: clinically significant renal dysfunction
- General disorders and administration site conditions: swelling and peripheral edema
- Laboratory abnormalities: gamma-glutamyltransferase increased
Cyclosporine: In two adult clinical studies, cyclosporine (one 4 mg/kg dose or two 3 mg/kg doses) increased the AUC of Cancidas. Cancidas did not increase the plasma levels of cyclosporine. There were transient increases in liver ALT and AST when Cancidas and cyclosporine were co-administered. Monitor patients who develop abnormal liver enzymes during concomitant therapy and evaluate the risk/benefit of continuing therapy [see Warnings and Precautions (5.2) and Clinical Pharmacology (12.3)].
Tacrolimus: For patients receiving Cancidas and tacrolimus, standard monitoring of tacrolimus trough whole blood concentrations and appropriate tacrolimus dosage adjustments are recommended.
Inducers of Hepatic CYP Enzymes
Rifampin: Rifampin is a potent CYP3A4 inducer and concomitant administration with Cancidas is expected to reduce the plasma concentrations of Cancidas. Therefore, adult patients on rifampin should receive 70 mg of Cancidas daily and pediatric patients on rifampin should receive 70 mg/m2 of Cancidas daily (not to exceed an actual daily dose of 70 mg) [see Dosage and Administration (2.5) and Clinical Pharmacology (12.3)].
Other Inducers of Hepatic CYP Enzymes
Adults: When Cancidas is co-administered to adult patients with other inducers of hepatic CYP enzymes, such as efavirenz, nevirapine, phenytoin, dexamethasone, or carbamazepine, administration of a daily dose of 70 mg of Cancidas should be considered [see Dosage and Administration (2.5) and Clinical Pharmacology (12.3)].
Pediatric Patients: When Cancidas is co-administered to pediatric patients with other inducers of hepatic CYP enzymes, such as efavirenz, nevirapine, phenytoin, dexamethasone, or carbamazepine, administration of a daily dose of 70 mg/m2 Cancidas (not to exceed an actual daily dose of 70 mg) should be considered [see Dosage and Administration (2.5) and Clinical Pharmacology (12.3)].
USE IN SPECIFIC POPULATIONS
Pregnancy Category C
There are no adequate and well-controlled studies with the use of Cancidas in pregnant women. In animal studies, caspofungin caused embryofetal toxicity, including increased resorptions, increased peri-implantation loss, and incomplete ossification at multiple fetal sites. Cancidas should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.
In offspring born to pregnant rats treated with caspofungin at doses comparable to the human dose based on body surface area comparisons, there was incomplete ossification of the skull and torso and increased incidences of cervical rib. There was also an increase in resorptions and peri-implantation losses. In pregnant rabbits treated with caspofungin at doses comparable to 2 times the human dose based on body surface area comparisons, there was an increased incidence of incomplete ossification of the talus/calcaneus in offspring and increases in fetal resorptions. Caspofungin crossed the placenta in rats and rabbits and was detectable in fetal plasma.
It is not known whether caspofungin is present in human milk. Caspofungin was found in the milk of lactating, drug-treated rats. Because many drugs are excreted in human milk, caution should be exercised when caspofungin is administered to a nursing woman.
The safety and effectiveness of Cancidas in pediatric patients 3 months to 17 years of age are supported by evidence from adequate and well-controlled studies in adults, pharmacokinetic data in pediatric patients, and additional data from prospective studies in pediatric patients 3 months to 17 years of age for the following indications [see Indications and Usage (1)]:
- Empirical therapy for presumed fungal infections in febrile, neutropenic patients.
- Treatment of candidemia and the following Candida infections: intra-abdominal abscesses, peritonitis, and pleural space infections.
- Treatment of esophageal candidiasis.
- Treatment of invasive aspergillosis in patients who are refractory to or intolerant of other therapies (e.g., amphotericin B, lipid formulations of amphotericin B, itraconazole).
The efficacy and safety of Cancidas has not been adequately studied in prospective clinical trials involving neonates and infants under 3 months of age. Although limited pharmacokinetic data were collected in neonates and infants below 3 months of age, these data are insufficient to establish a safe and effective dose of caspofungin in the treatment of neonatal candidiasis. Invasive candidiasis in neonates has a higher rate of CNS and multi-organ involvement than in older patients; the ability of Cancidas to penetrate the blood-brain barrier and to treat patients with meningitis and endocarditis is unknown.
Cancidas has not been studied in pediatric patients with endocarditis, osteomyelitis, and meningitis due to Candida. Cancidas has also not been studied as initial therapy for invasive aspergillosis in pediatric patients.
In clinical trials, 171 pediatric patients (0 months to 17 years of age), including 18 patients who were less than 3 months of age, were given intravenous Cancidas. Pharmacokinetic studies enrolled a total of 66 pediatric patients, and an additional 105 pediatric patients received Cancidas in safety and efficacy studies [see Clinical Pharmacology (12.3) and Clinical Studies (14.5)]. The majority of the pediatric patients received Cancidas at a once-daily maintenance dose of 50 mg/m2 for a mean duration of 12 days (median 9, range 1-87 days). In all studies, safety was assessed by the investigator throughout study therapy and for 14 days following cessation of study therapy. The most common adverse reactions in pediatric patients treated with Cancidas were pyrexia (29%), blood potassium decreased (15%), diarrhea (14%), increased aspartate aminotransferase (12%), rash (12%), increased alanine aminotransferase (11%), hypotension (11%), and chills (11%) [see Adverse Reactions (6.2)].
Postmarketing hepatobiliary adverse reactions have been reported in pediatric patients with serious underlying medical conditions [see Warnings and Precautions (5.3)].
Clinical studies of Cancidas did not include sufficient numbers of patients aged 65 and over to determine whether they respond differently from younger patients. Although the number of elderly patients was not large enough for a statistical analysis, no overall differences in safety or efficacy were observed between these and younger patients. Plasma concentrations of caspofungin in healthy older men and women (65 years of age and older) were increased slightly (approximately 28% in AUC) compared to young healthy men. A similar effect of age on pharmacokinetics was seen in patients with candidemia or other Candida infections (intra-abdominal abscesses, peritonitis, or pleural space infections). No dose adjustment is recommended for the elderly; however, greater sensitivity of some older individuals cannot be ruled out.
Patients with Hepatic Impairment
Adult patients with mild hepatic impairment (Child-Pugh score 5 to 6) do not need a dosage adjustment. For adult patients with moderate hepatic impairment (Child-Pugh score 7 to 9), Cancidas 35 mg once daily is recommended based upon pharmacokinetic data [see Clinical Pharmacology (12.3)]. However, where recommended, a 70-mg loading dose should still be administered on Day 1 [see Dosage and Administration (2.4) and Clinical Pharmacology (12.3)]. There is no clinical experience in adult patients with severe hepatic impairment (Child-Pugh score greater than 9) and in pediatric patients 3 months to 17 years of age with any degree of hepatic impairment.
Patients with Renal Impairment
No dosage adjustment is necessary for patients with renal impairment. Caspofungin is not dialyzable; thus, supplementary dosing is not required following hemodialysis [see Clinical Pharmacology (12.3)].
In 6 healthy subjects who received a single 210-mg dose, no significant adverse reactions were reported. Multiple doses above 150 mg daily have not been studied. Caspofungin is not dialyzable.
In clinical trials, one pediatric patient (16 years of age) unintentionally received a single dose of caspofungin of 113 mg (on Day 1), followed by 80 mg daily for an additional 7 days. No clinically significant adverse reactions were reported.
Cancidas is a sterile, lyophilized product for intravenous (IV) infusion that contains a semisynthetic lipopeptide (echinocandin) compound synthesized from a fermentation product of Glarea lozoyensis. Cancidas is an echinocandin antifungal that inhibits the synthesis of β (1,3)-D-glucan, an integral component of the fungal cell wall.
Cancidas (caspofungin acetate) is 1-[(4R,5S)-5-[(2-aminoethyl)amino]-N2-(10,12-dimethyl-1-oxotetradecyl)-4-hydroxy-L-ornithine]-5-[(3R)-3-hydroxy-L-ornithine] pneumocandin B0 diacetate (salt). Cancidas 50 mg also contains: 39 mg sucrose, 26 mg mannitol, glacial acetic acid, and sodium hydroxide. Cancidas 70 mg also contains 54 mg sucrose, 36 mg mannitol, glacial acetic acid, and sodium hydroxide. Caspofungin acetate is a hygroscopic, white to off-white powder. It is freely soluble in water and methanol, and slightly soluble in ethanol. The pH of a saturated aqueous solution of caspofungin acetate is approximately 6.6. The empirical formula is C52H88N10O15∙2C2H4O2 and the formula weight is 1213.42. The structural formula is:
Cancidas - Clinical Pharmacology
Mechanism of Action
Caspofungin is an echinocandin antifungal drug [see Microbiology (12.4)].
Adult and pediatric pharmacokinetic parameters are presented in Table 8.
Plasma concentrations of caspofungin decline in a polyphasic manner following single 1-hour IV infusions. A short α-phase occurs immediately postinfusion, followed by a β-phase (half-life of 9 to 11 hours) that characterizes much of the profile and exhibits clear log-linear behavior from 6 to 48 hours postdose during which the plasma concentration decreases 10-fold. An additional, longer half-life phase, γ-phase, (half-life of 40-50 hours), also occurs. Distribution, rather than excretion or biotransformation, is the dominant mechanism influencing plasma clearance. Caspofungin is extensively bound to albumin (~97%), and distribution into red blood cells is minimal. Mass balance results showed that approximately 92% of the administered radioactivity was distributed to tissues by 36 to 48 hours after a single 70-mg dose of [3H] Cancidas. There is little excretion or biotransformation of caspofungin during the first 30 hours after administration.
Caspofungin is slowly metabolized by hydrolysis and N-acetylation. Caspofungin also undergoes spontaneous chemical degradation to an open-ring peptide compound, L-747969. At later time points (≥5 days postdose), there is a low level (≤7 picomoles/mg protein, or ≤1.3% of administered dose) of covalent binding of radiolabel in plasma following single-dose administration of [3H] Cancidas, which may be due to two reactive intermediates formed during the chemical degradation of caspofungin to L-747969. Additional metabolism involves hydrolysis into constitutive amino acids and their degradates, including dihydroxyhomotyrosine and N-acetyl-dihydroxyhomotyrosine. These two tyrosine derivatives are found only in urine, suggesting rapid clearance of these derivatives by the kidneys.
Two single-dose radiolabeled pharmacokinetic studies were conducted. In one study, plasma, urine, and feces were collected over 27 days, and in the second study plasma was collected over 6 months. Plasma concentrations of radioactivity and of caspofungin were similar during the first 24 to 48 hours postdose; thereafter drug levels fell more rapidly. In plasma, caspofungin concentrations fell below the limit of quantitation after 6 to 8 days postdose, while radiolabel fell below the limit of quantitation at 22.3 weeks postdose. After single intravenous administration of [3H] Cancidas, excretion of caspofungin and its metabolites in humans was 35% of dose in feces and 41% of dose in urine. A small amount of caspofungin is excreted unchanged in urine (~1.4% of dose). Renal clearance of parent drug is low (~0.15 mL/min) and total clearance of caspofungin is 12 mL/min.
In a clinical study of single 70-mg doses, caspofungin pharmacokinetics were similar in healthy adult volunteers with mild renal impairment (creatinine clearance 50 to 80 mL/min) and control subjects. Moderate (creatinine clearance 31 to 49 mL/min), severe (creatinine clearance 5 to 30 mL/min), and end-stage (creatinine clearance less than 10 mL/min and dialysis dependent) renal impairment moderately increased caspofungin plasma concentrations after single-dose administration (range: 30 to 49% for AUC). However, in adult patients with invasive aspergillosis, candidemia, or other Candida infections (intra-abdominal abscesses, peritonitis, or pleural space infections) who received multiple daily doses of Cancidas 50 mg, there was no significant effect of mild to end-stage renal impairment on caspofungin concentrations. No dosage adjustment is necessary for patients with renal impairment. Caspofungin is not dialyzable, thus supplementary dosing is not required following hemodialysis.
Plasma concentrations of caspofungin after a single 70-mg dose in adult patients with mild hepatic impairment (Child-Pugh score 5 to 6) were increased by approximately 55% in AUC compared to healthy control subjects. In a 14-day multiple-dose study (70 mg on Day 1 followed by 50 mg daily thereafter), plasma concentrations in adult patients with mild hepatic impairment were increased modestly (19 to 25% in AUC) on Days 7 and 14 relative to healthy control subjects. No dosage adjustment is recommended for patients with mild hepatic impairment.
Adult patients with moderate hepatic impairment (Child-Pugh score 7 to 9) who received a single 70-mg dose of Cancidas had an average plasma caspofungin increase of 76% in AUC compared to control subjects. A dosage reduction is recommended for adult patients with moderate hepatic impairment based upon these pharmacokinetic data [see Dosage and Administration (2.4)].
There is no clinical experience in adult patients with severe hepatic impairment (Child-Pugh score greater than 9) or in pediatric patients with any degree of hepatic impairment.
Plasma concentrations of caspofungin in healthy adult men and women were similar following a single 70-mg dose. After 13 daily 50-mg doses, caspofungin plasma concentrations in women were elevated slightly (approximately 22% in area under the curve [AUC]) relative to men. No dosage adjustment is necessary based on gender.
Regression analyses of patient pharmacokinetic data indicated that no clinically significant differences in the pharmacokinetics of caspofungin were seen among Caucasians, Blacks, and Hispanics. No dosage adjustment is necessary on the basis of race.
Plasma concentrations of caspofungin in healthy older men and women (65 years of age and older) were increased slightly (approximately 28% AUC) compared to young healthy men after a single 70-mg dose of caspofungin. In patients who were treated empirically or who had candidemia or other Candida infections (intra-abdominal abscesses, peritonitis, or pleural space infections), a similar modest effect of age was seen in older patients relative to younger patients. No dosage adjustment is necessary for the elderly [see Use in Specific Populations (8.5)].
Cancidas has been studied in five prospective studies involving pediatric patients under 18 years of age, including three pediatric pharmacokinetic studies [initial study in adolescents (12-17 years of age) and children (2-11 years of age) followed by a study in younger patients (3-23 months of age) and then followed by a study in neonates and infants (less than 3 months of age)] [see Use in Specific Populations (8.4)].
Pharmacokinetic parameters following multiple doses of Cancidas in pediatric and adult patients are presented in Table 8.
|Population||N||Daily Dose||Pharmacokinetic Parameters
(Mean ± Standard Deviation)
|Adolescents, Aged 12-17 years||8||50 mg/m2||124.9 ± 50.4||14.0 ± 6.9||2.4 ± 1.0||11.2 ± 1.7||12.6 ± 5.5|
|Children, Aged 2-11 years||9||50 mg/m2||120.0 ± 33.4||16.1 ± 4.2||1.7 ± 0.8||8.2 ± 2.4||6.4 ± 2.6|
|Young Children, Aged 3-23 months||8||50 mg/m2||131.2 ± 17.7||17.6 ± 3.9||1.7 ± 0.7||8.8 ± 2.1||3.2 ± 0.4|
|Adults with Esophageal Candidiasis||6†||50 mg||87.3 ± 30.0||8.7 ± 2.1||1.7 ± 0.7||13.0 ± 1.9||10.6 ± 3.8|
|Adults receiving Empirical Therapy||119‡||50 mg§||--||8.0 ± 3.4||1.6 ± 0.7||--||--|
Drug Interactions [see Drug Interactions (7)]
Studies in vitro show that caspofungin acetate is not an inhibitor of any enzyme in the cytochrome P (CYP) system. Caspofungin is not a substrate for P-glycoprotein and is a poor substrate for CYP enzymes.
In clinical studies, caspofungin did not induce the CYP3A4 metabolism of other drugs. Clinical studies in adult healthy volunteers also demonstrated that the pharmacokinetics of caspofungin are not altered by itraconazole, amphotericin B, mycophenolate, nelfinavir, or tacrolimus. Caspofungin has no effect on the pharmacokinetics of itraconazole, amphotericin B, or the active metabolite of mycophenolate.
Cyclosporine: In two adult clinical studies, cyclosporine (one 4 mg/kg dose or two 3 mg/kg doses) increased the AUC of caspofungin by approximately 35%. Cancidas did not increase the plasma levels of cyclosporine. There were transient increases in liver ALT and AST when Cancidas and cyclosporine were co-administered [see Warnings and Precautions (5.2)].
Tacrolimus: Cancidas reduced the blood AUC0-12 of tacrolimus (FK-506, Prograf®) by approximately 20%, peak blood concentration (Cmax) by 16%, and 12-hour blood concentration (C12hr) by 26% in healthy adult subjects when tacrolimus (2 doses of 0.1 mg/kg 12 hours apart) was administered on the 10th day of Cancidas 70 mg daily, as compared to results from a control period in which tacrolimus was administered alone. For patients receiving both therapies, standard monitoring of tacrolimus whole blood trough concentrations and appropriate tacrolimus dosage adjustments are recommended.
Rifampin: A drug-drug interaction study with rifampin in adult healthy volunteers has shown a 30% decrease in caspofungin trough concentrations [see Dosage and Administration (2.5)].
Other Inducers of Hepatic CYP Enzymes
Adults: Results from regression analyses of adult patient pharmacokinetic data suggest that co-administration of other hepatic CYP enzyme inducers (e.g., efavirenz, nevirapine, phenytoin, dexamethasone, or carbamazepine) with Cancidas may result in clinically meaningful reductions in caspofungin concentrations. It is not known which drug clearance mechanism involved in caspofungin disposition may be inducible [see Dosage and Administration (2.5)].
Pediatric patients: In pediatric patients, results from regression analyses of pharmacokinetic data suggest that co-administration of dexamethasone with Cancidas may result in clinically meaningful reductions in caspofungin trough concentrations. This finding may indicate that pediatric patients will have similar reductions with inducers as seen in adults [see Dosage and Administration (2.5)].
Mechanism of Action
Caspofungin, an echinocandin, inhibits the synthesis of beta (1,3)-D-glucan, an essential component of the cell wall of susceptible Aspergillus species and Candida species. Beta (1,3)-D-glucan is not present in mammalian cells. Caspofungin has shown activity against Candida species and in regions of active cell growth of the hyphae of Aspergillus fumigatus.
There have been reports of clinical failures in patients receiving caspofungin therapy due to the development of drug resistance. Some of these reports have identified specific mutations in the Fks subunits of the glucan synthase enzyme. These mutations are associated with higher MICs and breakthrough infection. Candida species that exhibit reduced susceptibility to caspofungin as a result of an increase in the chitin content of the fungal cell wall have also been identified, although the significance of this phenomenon in vivo is not well known.
Studies in vitro and in vivo of caspofungin, in combination with amphotericin B, suggest no antagonism of antifungal activity against either A. fumigatus or C. albicans. The clinical significance of these results is unknown.
Activity in Vitro and in Clinical Infections
Caspofungin has been shown to be active both in vitro and in clinical infections against most strains of the following microorganisms:
- Aspergillus fumigatus
- Aspergillus flavus
- Aspergillus terreus
- Candida albicans
- Candida glabrata
- Candida guilliermondii
- Candida krusei
- Candida parapsilosis
- Candida tropicalis
Susceptibility Testing Methods
The interpretive standards for caspofungin against Candida species are applicable only to tests performed using Clinical Laboratory and Standards Institute (CLSI) microbroth dilution reference methods2,3 for MIC (partial inhibition endpoint) read at 24 hours. No interpretive criteria have been established for Aspergillus species or other filamentous fungi.
When available, the clinical microbiology laboratory should provide the results of in vitro susceptibility test results for antimicrobial drug products used in resident hospitals to the physician as periodic reports that describe the susceptibility profile of pathogens. These reports should aid the physician in selecting an antifungal drug product for treatment. The techniques for Broth Microdilution are described below.
Broth Microdilution Techniques
Quantitative methods are used to determine antifungal minimum inhibitory concentrations (MICs). These MICs provide estimates of the susceptibility of Candida spp. to antifungal agents. MICs should be determined using a standardized procedure at 24 hours2,3. Standardized procedures are based on a microdilution method (broth) with standardized inoculum concentrations and standardized concentrations of caspofungin powder. The MIC values should be interpreted according to the criteria provided in Table 9.
|Pathogen||Broth Microdilution MIC* (mcg/mL) at 24 hours|
|Susceptible (S)||Non-Susceptible (NS)|
Standardized susceptibility test procedures require the use of quality control organisms to control the technical aspects of the test procedures. Standard caspofungin powder should provide the following range of values noted in Table 103. Quality control microorganisms are specific strains of organisms with intrinsic biological properties relating to resistance mechanisms and their genetic expression within fungi; the specific strains used for microbiological control are not clinically significant.
|QC Strain||Broth Microdilution
(MIC in mcg/mL) at 24 hours*
|Candida parapsilosis ATCC 22019||0.25 – 1.0|
|Candida krusei ATCC 6258||0.12 – 1.0|
Carcinogenesis, Mutagenesis, Impairment of Fertility
No long-term studies in animals have been performed to evaluate the carcinogenic potential of caspofungin.
Caspofungin did not show evidence of mutagenic or genotoxic potential when evaluated in the following in vitro assays: bacterial (Ames) and mammalian cell (V79 Chinese hamster lung fibroblasts) mutagenesis assays, the alkaline elution/rat hepatocyte DNA strand break test, and the chromosome aberration assay in Chinese hamster ovary cells. Caspofungin was not genotoxic when assessed in the mouse bone marrow chromosomal test at doses up to 12.5 mg/kg (equivalent to a human dose of 1 mg/kg based on body surface area comparisons), administered intravenously.
Fertility and reproductive performance were not affected by the intravenous administration of caspofungin to rats at doses up to 5 mg/kg. At 5 mg/kg exposures were similar to those seen in patients treated with the 70-mg dose.
Animal Toxicology and/or Pharmacology
In one 5-week study in monkeys at doses which produced exposures approximately 4 to 6 times those seen in adult patients treated with a 70-mg dose, scattered small foci of subcapsular necrosis were observed microscopically in the livers of some animals (2/8 monkeys at 5 mg/kg and 4/8 monkeys at 8 mg/kg); however, this histopathological finding was not seen in another study of 27 weeks duration at similar doses.
No treatment-related findings were seen in a 5-week study in infant monkeys at doses which produced exposures approximately 3 times those achieved in pediatric patients receiving a maintenance dose of 50 mg/m2 daily.
Empirical Therapy in Febrile, Neutropenic Patients
A double-blind study enrolled 1111 febrile, neutropenic (<500 cells/mm3) patients who were randomized to treatment with daily doses of Cancidas (50 mg/day following a 70-mg loading dose on Day 1) or AmBisome (3 mg/kg/day). Patients were stratified based on risk category (high-risk patients had undergone allogeneic stem cell transplantation or had relapsed acute leukemia) and on receipt of prior antifungal prophylaxis. Twenty-four percent of patients were high risk and 56% had received prior antifungal prophylaxis. Patients who remained febrile or clinically deteriorated following 5 days of therapy could receive 70 mg/day of Cancidas or 5 mg/kg/day of AmBisome. Treatment was continued to resolution of neutropenia (but not beyond 28 days unless a fungal infection was documented).
An overall favorable response required meeting each of the following criteria: no documented breakthrough fungal infections up to 7 days after completion of treatment, survival for 7 days after completion of study therapy, no discontinuation of the study drug because of drug-related toxicity or lack of efficacy, resolution of fever during the period of neutropenia, and successful treatment of any documented baseline fungal infection.
Based on the composite response rates, Cancidas was as effective as AmBisome in empirical therapy of persistent febrile neutropenia (see Table 11).
|Number of Patients‡||556||539|
|Overall Favorable Response||190 (33.9%)||181 (33.7%)||0.2 (-5.6, 6.0)|
|No documented breakthrough fungal infection||527 (94.8%)||515 (95.5%)||-0.8|
|Survival 7 days after end of treatment||515 (92.6%)||481 (89.2%)||3.4|
|No discontinuation due to toxicity or lack of efficacy||499 (89.7%)||461 (85.5%)||4.2|
|Resolution of fever during neutropenia||229 (41.2%)||223 (41.4%)||-0.2|
The rate of successful treatment of documented baseline infections, a component of the primary endpoint, was not statistically different between treatment groups.
The response rates did not differ between treatment groups based on either of the stratification variables: risk category or prior antifungal prophylaxis.
Candidemia and the Following other Candida Infections: Intra-Abdominal Abscesses, Peritonitis and Pleural Space Infections
In a randomized, double-blind study, patients with a proven diagnosis of invasive candidiasis received daily doses of Cancidas (50 mg/day following a 70-mg loading dose on Day 1) or amphotericin B deoxycholate (0.6 to 0.7 mg/kg/day for non-neutropenic patients and 0.7 to 1 mg/kg/day for neutropenic patients). Patients were stratified by both neutropenic status and APACHE II score. Patients with Candida endocarditis, meningitis, or osteomyelitis were excluded from this study.
Patients who met the entry criteria and received one or more doses of IV study therapy were included in the modified intention-to-treat [MITT] analysis of response at the end of IV study therapy. A favorable response at this time point required both symptom/sign resolution/improvement and microbiological clearance of the Candida infection.
Two hundred thirty-nine patients were enrolled. Patient disposition is shown in Table 12.
|Patients completing study†||63 (55.3%)||69 (55.2%)|
|DISCONTINUATIONS OF STUDY†|
|All Study Discontinuations||51 (44.7%)||56 (44.8%)|
|Study Discontinuations due to clinical adverse events||39 (34.2%)||43 (34.4%)|
|Study Discontinuations due to laboratory adverse events||0 (0%)||1 (0.8%)|
|DISCONTINUATIONS OF STUDY THERAPY|
|All Study Therapy Discontinuations||48 (42.1%)||58 (46.4%)|
|Study Therapy Discontinuations due to clinical adverse events||30 (26.3%)||37 (29.6%)|
|Study Therapy Discontinuations due to laboratory adverse events||1 (0.9%)||7 (5.6%)|
|Study Therapy Discontinuations due to all drug-related‡ adverse events||3 (2.6%)||29 (23.2%)|
Of the 239 patients enrolled, 224 met the criteria for inclusion in the MITT population (109 treated with Cancidas and 115 treated with amphotericin B). Of these 224 patients, 186 patients had candidemia (92 treated with Cancidas and 94 treated with amphotericin B). The majority of the patients with candidemia were non-neutropenic (87%) and had an APACHE II score less than or equal to 20 (77%) in both arms. Most candidemia infections were caused by C. albicans (39%), followed by C. parapsilosis (20%), C. tropicalis (17%), C. glabrata (8%), and C. krusei (3%).
At the end of IV study therapy, Cancidas was comparable to amphotericin B in the treatment of candidemia in the MITT population. For the other efficacy time points (Day 10 of IV study therapy, end of all antifungal therapy, 2-week post-therapy follow-up, and 6- to 8-week post-therapy follow-up), Cancidas was as effective as amphotericin B.
Outcome, relapse and mortality data are shown in Table 13.
|Cancidas*||Amphotericin B||% Difference† after adjusting for strata
|Number of MITT§ patients||109||115|
|FAVORABLE OUTCOMES (MITT) AT THE END OF IV STUDY THERAPY|
|All MITT patients||81/109 (74.3%)||78/115 (67.8%)||7.5 (-5.4, 20.3)|
|Candidemia||67/92 (72.8%)||63/94 (67.0%)||7.0 (-7.0, 21.1)|
|Neutropenic||6/14 (43%)||5/10 (50%)|
|Non-neutropenic||61/78 (78%)||58/84 (69%)|
|Blood / Pleural||1/1||1/1|
|Blood / Peritoneal||1/1||1/1|
|Blood / Urine||-||1/1|
|Peritoneal / Pleural||1/2||-|
|Abdominal / Peritoneal||-||1/1|
|Subphrenic / Peritoneal||1/1||-|
|DISSEMINATED INFECTIONS, RELAPSES AND MORTALITY|
|Disseminated Infections in neutropenic patients||4/14 (28.6%)||3/10 (30.0%)|
|All relapses¶||7/81 (8.6%)||8/78 (10.3%)|
|Culture-confirmed relapse||5/81 (6%)||2/78 (3%)|
|Overall study# mortality in MITT||36/109 (33.0%)||35/115 (30.4%)|
|Mortality during study therapy||18/109 (17%)||13/115 (11%)|
|Mortality attributed to Candida||4/109 (4%)||7/115 (6%)|
In this study, the efficacy of Cancidas in patients with intra-abdominal abscesses, peritonitis and pleural space Candida infections was evaluated in 19 non-neutropenic patients. Two of these patients had concurrent candidemia. Candida was part of a polymicrobial infection that required adjunctive surgical drainage in 11 of these 19 patients. A favorable response was seen in 9 of 9 patients with peritonitis, 3 of 4 with abscesses (liver, parasplenic, and urinary bladder abscesses), 2 of 2 with pleural space infections, 1 of 2 with mixed peritoneal and pleural infection, 1 of 1 with mixed abdominal abscess and peritonitis, and 0 of 1 with Candida pneumonia.
Overall, across all sites of infection included in the study, the efficacy of Cancidas was comparable to that of amphotericin B for the primary endpoint.
In this study, the efficacy data for Cancidas in neutropenic patients with candidemia were limited. In a separate compassionate use study, 4 patients with hepatosplenic candidiasis received prolonged therapy with Cancidas following other long-term antifungal therapy; three of these patients had a favorable response.
In a second randomized, double-blind study, 197 patients with proven invasive candidiasis received Cancidas 50 mg/day (following a 70-mg loading dose on Day 1) or Cancidas 150 mg/day. The diagnostic criteria, evaluation time points, and efficacy endpoints were similar to those employed in the prior study. Patients with Candida endocarditis, meningitis, or osteomyelitis were excluded. Although this study was designed to compare the safety of the two doses, it was not large enough to detect differences in rare or unexpected adverse events [see Adverse Reactions (6.1)]. The efficacy of Cancidas at the 150 mg daily dose was not significantly better than the efficacy of the 50-mg daily dose of Cancidas. The efficacy of doses higher than 50 mg daily in the other adult patients for whom Cancidas is indicated has not been evaluated.
Esophageal Candidiasis (and information on oropharyngeal candidiasis)
The safety and efficacy of Cancidas in the treatment of esophageal candidiasis was evaluated in one large, controlled, noninferiority, clinical trial and two smaller dose-response studies.
In all 3 studies, patients were required to have symptoms and microbiological documentation of esophageal candidiasis; most patients had advanced AIDS (with CD4 counts <50/mm3).
Of the 166 patients in the large study who had culture-confirmed esophageal candidiasis at baseline, 120 had Candida albicans and 2 had Candida tropicalis as the sole baseline pathogen whereas 44 had mixed baseline cultures containing C. albicans and one or more additional Candida species.
In the large, randomized, double-blind study comparing Cancidas 50 mg/day versus intravenous fluconazole 200 mg/day for the treatment of esophageal candidiasis, patients were treated for an average of 9 days (range 7-21 days). Favorable overall response at 5 to 7 days following discontinuation of study therapy required both complete resolution of symptoms and significant endoscopic improvement. The definition of endoscopic response was based on severity of disease at baseline using a 4-grade scale and required at least a two-grade reduction from baseline endoscopic score or reduction to grade 0 for patients with a baseline score of 2 or less.
The proportion of patients with a favorable overall response was comparable for Cancidas and fluconazole as shown in Table 14.
|Day 5-7 post-treatment||66/81 (81.5%)||80/94 (85.1%)||-3.6 (-14.7, 7.5)|
The proportion of patients with a favorable symptom response was also comparable (90.1% and 89.4% for Cancidas and fluconazole, respectively). In addition, the proportion of patients with a favorable endoscopic response was comparable (85.2% and 86.2% for Cancidas and fluconazole, respectively).
As shown in Table 15, the esophageal candidiasis relapse rates at the Day 14 post-treatment visit were similar for the two groups. At the Day 28 post-treatment visit, the group treated with Cancidas had a numerically higher incidence of relapse; however, the difference was not statistically significant.
|Day 14 post-treatment||7/66 (10.6%)||6/76 (7.9%)||2.7 (-6.9, 12.3)|
|Day 28 post-treatment||18/64 (28.1%)||12/72 (16.7%)||11.5 (-2.5, 25.4)|
In this trial, which was designed to establish noninferiority of Cancidas to fluconazole for the treatment of esophageal candidiasis, 122 (70%) patients also had oropharyngeal candidiasis. A favorable response was defined as complete resolution of all symptoms of oropharyngeal disease and all visible oropharyngeal lesions. The proportion of patients with a favorable oropharyngeal response at the 5- to 7-day post-treatment visit was numerically lower for Cancidas; however, the difference was not statistically significant. Oropharyngeal candidiasis relapse rates at Day 14 and Day 28 post-treatment visits were statistically significantly higher for Cancidas than for fluconazole. The results are shown in Table 16.
|Response Rate Day 5-7 post-treatment||40/56 (71.4%)||55/66 (83.3%)||-11.9 (-26.8, 3.0)|
|Relapse Rate Day 14 post-treatment||17/40 (42.5%)||7/53 (13.2%)||29.3 (11.5, 47.1)|
|Relapse Rate Day 28 post-treatment||23/39 (59.0%)||18/51 (35.3%)||23.7 (3.4, 43.9)|
The results from the two smaller dose-ranging studies corroborate the efficacy of Cancidas for esophageal candidiasis that was demonstrated in the larger study.
Cancidas was associated with favorable outcomes in 7 of 10 esophageal C. albicans infections refractory to at least 200 mg of fluconazole given for 7 days, although the in vitro susceptibility of the infecting isolates to fluconazole was not known.
Sixty-nine patients between the ages of 18 and 80 with invasive aspergillosis were enrolled in an open-label, noncomparative study to evaluate the safety, tolerability, and efficacy of Cancidas. Enrolled patients had previously been refractory to or intolerant of other antifungal therapy(ies). Refractory patients were classified as those who had disease progression or failed to improve despite therapy for at least 7 days with amphotericin B, lipid formulations of amphotericin B, itraconazole, or an investigational azole with reported activity against Aspergillus. Intolerance to previous therapy was defined as a doubling of creatinine (or creatinine ≥2.5 mg/dL while on therapy), other acute reactions, or infusion-related toxicity. To be included in the study, patients with pulmonary disease must have had definite (positive tissue histopathology or positive culture from tissue obtained by an invasive procedure) or probable (positive radiographic or computed tomography evidence with supporting culture from bronchoalveolar lavage or sputum, galactomannan enzyme-linked immunosorbent assay, and/or polymerase chain reaction) invasive aspergillosis. Patients with extrapulmonary disease had to have definite invasive aspergillosis. Patients were administered a single 70-mg loading dose of Cancidas and subsequently dosed with 50 mg daily. The mean duration of therapy was 33.7 days, with a range of 1 to 162 days.
An independent expert panel evaluated patient data, including diagnosis of invasive aspergillosis, response and tolerability to previous antifungal therapy, treatment course on Cancidas, and clinical outcome.
A favorable response was defined as either complete resolution (complete response) or clinically meaningful improvement (partial response) of all signs and symptoms and attributable radiographic findings. Stable, nonprogressive disease was considered to be an unfavorable response.
Among the 69 patients enrolled in the study, 63 met entry diagnostic criteria and had outcome data; and of these, 52 patients received treatment for greater than 7 days. Fifty-three (84%) were refractory to previous antifungal therapy and 10 (16%) were intolerant. Forty-five patients had pulmonary disease and 18 had extrapulmonary disease. Underlying conditions were hematologic malignancy (N=24), allogeneic bone marrow transplant or stem cell transplant (N=18), organ transplant (N=8), solid tumor (N=3), or other conditions (N=10). All patients in the study received concomitant therapies for their other underlying conditions. Eighteen patients received tacrolimus and Cancidas concomitantly, of whom 8 also received mycophenolate mofetil.
Overall, the expert panel determined that 41% (26/63) of patients receiving at least one dose of Cancidas had a favorable response. For those patients who received greater than 7 days of therapy with Cancidas, 50% (26/52) had a favorable response. The favorable response rates for patients who were either refractory to or intolerant of previous therapies were 36% (19/53) and 70% (7/10), respectively. The response rates among patients with pulmonary disease and extrapulmonary disease were 47% (21/45) and 28% (5/18), respectively. Among patients with extrapulmonary disease, 2 of 8 patients who also had definite, probable, or possible CNS involvement had a favorable response. Two of these 8 patients had progression of disease and manifested CNS involvement while on therapy.
Cancidas is effective for the treatment of invasive aspergillosis in patients who are refractory to or intolerant of itraconazole, amphotericin B, and/or lipid formulations of amphotericin B. However, the efficacy of Cancidas for initial treatment of invasive aspergillosis has not been evaluated in comparator-controlled clinical studies.
The safety and efficacy of Cancidas were evaluated in pediatric patients 3 months to 17 years of age in two prospective, multicenter clinical trials.
The first study, which enrolled 82 patients between 2 to 17 years of age, was a randomized, double-blind study comparing Cancidas (50 mg/m2 IV once daily following a 70-mg/m2 loading dose on Day 1 [not to exceed 70 mg daily]) to AmBisome (3 mg/kg IV daily) in a 2:1 treatment fashion (56 on caspofungin, 26 on AmBisome) as empirical therapy in pediatric patients with persistent fever and neutropenia. The study design and criteria for efficacy assessment were similar to the study in adult patients [see Clinical Studies (14.1)]. Patients were stratified based on risk category (high-risk patients had undergone allogeneic stem cell transplantation or had relapsed acute leukemia). Twenty-seven percent of patients in both treatment groups were high risk. Favorable overall response rates of pediatric patients with persistent fever and neutropenia are presented in Table 17.
|Number of Patients||56||25|
|Overall Favorable Response||26/56 (46.4%)||8/25 (32.0%)|
|High risk||9/15 (60.0%)||0/7 (0.0%)|
|Low risk||17/41 (41.5%)||8/18 (44.4%)|
The second study was a prospective, open-label, non-comparative study estimating the safety and efficacy of caspofungin in pediatric patients (ages 3 months to 17 years) with candidemia and other Candida infections, esophageal candidiasis, and invasive aspergillosis (as salvage therapy). The study employed diagnostic criteria which were based on established EORTC/MSG criteria of proven or probable infection; these criteria were similar to those criteria employed in the adult studies for these various indications. Similarly, the efficacy time points and endpoints used in this study were similar to those employed in the corresponding adult studies [see Clinical Studies (14.2, 14.3, and 14.4)]. All patients received Cancidas at 50 mg/m2 IV once daily following a 70-mg/m2 loading dose on Day 1 (not to exceed 70 mg daily). Among the 49 enrolled patients who received Cancidas, 48 were included in the efficacy analysis (one patient excluded due to not having a baseline Aspergillus or Candida infection). Of these 48 patients, 37 had candidemia or other Candida infections, 10 had invasive aspergillosis, and 1 patient had esophageal candidiasis. Most candidemia and other Candida infections were caused by C. albicans (35%), followed by C. parapsilosis (22%), C. tropicalis (14%), and C. glabrata (11%). The favorable response rate, by indication, at the end of caspofungin therapy was as follows: 30/37 (81%) in candidemia or other Candida infections, 5/10 (50%) in invasive aspergillosis, and 1/1 in esophageal candidiasis.
- Mosteller RD: Simplified Calculation of Body Surface Area. N Engl J Med 1987 Oct 22;317(17): 1098 (letter).
- Clinical and Laboratory Standards Institute (CLSI). Reference Method for Broth Dilution Antifungal Susceptibility Testing of Yeasts; Approved Standard-Third Edition. CLSI document M27-A3. Clinical and Laboratory Standards Institute, 940 West Valley Road, Suite 1400, Wayne, Pennsylvania 19087, USA, 2008.
- Clinical and Laboratory Standards Institute (CLSI). Reference Method for Broth Dilution Antifungal Susceptibility Testing of Yeasts; Third Informational Supplement. CLSI document M27-S3. Clinical and Laboratory Standards Institute, 940 West Valley Road, Suite 1400, Wayne, Pennsylvania 19087, USA, 2008.
How Supplied/Storage and Handling
Cancidas 50 mg is a lyophilized white to off-white cake or powder for intravenous infusion supplied in single-dose vials with a red aluminum band and a plastic cap.
NDC 0006-3822-10 supplied as one single-use vial.
Cancidas 70 mg is a white to off-white powder/cake for infusion in a vial with a yellow/orange aluminum band and a plastic cap.
NDC 0006-3823-10 supplied as one single-use vial.
Storage and Handling
The lyophilized vials should be stored refrigerated at 2° to 8°C (36° to 46°F).
Patient Counseling Information
Inform patients that anaphylactic reactions have been reported during administration of Cancidas. Cancidas can cause hypersensitivity reactions, including rash, facial swelling, angioedema, pruritus, sensation of warmth, or bronchospasm. Inform patients to report these signs or symptoms to their healthcare providers.
Inform patients that there have been isolated reports of serious hepatic effects from Cancidas therapy.
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MERCK & CO., INC., Whitehouse Station, NJ 08889, USA
The trademarks depicted herein are owned by their respective companies.
Copyright © 2001-2017 Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.
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PRINCIPAL DISPLAY PANEL - 50 mg Vial Carton
FOR INTRAVENOUS USE ONLY
*Vial contains 54.6 mg of
caspofungin. Reconstitute with
10.8 mL of diluent to obtain a
concentration of 5 mg/mL.
Requires further dilution prior
DO NOT USE DILUENTS
PRINCIPAL DISPLAY PANEL - 70 mg Vial Carton
FOR INTRAVENOUS USE ONLY
*Vial contains 75.6 mg of
caspofungin. Reconstitute with
10.8 mL of diluent to obtain a
concentration of 7 mg/mL.
Requires further dilution prior
DO NOT USE DILUENTS
caspofungin acetate injection, powder, lyophilized, for solution
caspofungin acetate injection, powder, lyophilized, for solution
|Labeler - Merck Sharp & Dohme Corp. (001317601)|
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- Drug class: echinocandins