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AM B Isome (Amphotericin B) - Description and Clinical Pharmacology

 
 



DESCRIPTION

Am B isome for Injection is a sterile, non-pyrogenic lyophilized product for intravenous infusion. Each vial contains 50 mg of amphotericin B, USP, intercalated into a liposomal membrane consisting of approximately 213 mg hydrogenated soy phosphatidylcholine; 52 mg cholesterol, NF; 84 mg distearoylphosphatidylglycerol; 0.64 mg alpha tocopherol, USP; together with 900 mg sucrose, NF; and 27 mg disodium succinate hexahydrate as buffer. Following reconstitution with Sterile Water for Injection, USP, the resulting pH of the suspension is between 5-6.

Am B isome is a true single bilayer liposomal drug delivery system. Liposomes are closed, spherical vesicles created by mixing specific proportions of amphophilic substances such as phospholipids and cholesterol so that they arrange themselves into multiple concentric bilayer membranes when hydrated in aqueous solutions. Single bilayer liposomes are then formed by microemulsification of multilamellar vesicles using a homogenizer. Am B isome consists of these unilamellar bilayer liposomes with amphotericin B intercalated within the membrane. Due to the nature and quantity of amphophilic substances used, and the lipophilic moiety in the amphotericin B molecule, the drug is an integral part of the overall structure of the Am B isome liposomes. Am B isome contains true liposomes that are less than 100 nm in diameter. A schematic depiction of the liposome is presented below.

Note:   Liposomal encapsulation or incorporation into a lipid complex can substantially affect a drug's functional properties relative to those of the unencapsulated drug or non-lipid associated drug. In addition, different liposomal or lipid-complex products with a common active ingredient may vary from one another in the chemical composition and physical form of the lipid component. Such differences may affect the functional properties of these drug products.

Amphotericin B is a macrocyclic, polyene, antifungal antibiotic produced from a strain of Streptomyces nodosus.

Amphotericin B is designated chemically as:

[1R-(1R*,3S*,5R*,6R*,9R*,11R*,15S*,16R*,17R*,18S*,19E, 21E,23E,25E,27E,29E,31E,33R*,35S*,36R*,37S*)]-33-[(3-Amino-3,6-dideoxy-(beta)-D-mannopyranosyl)oxy]-1,3,5,6,9,11,17,37-octahydroxy-15,16,18-trimethyl-13-oxo-14,39-dioxabicyclo[33.3.1]nonatriaconta-19,21,23,25,27,29,31-heptaene-36-carboxylic acid (CAS No. 1397-89-3).

Amphotericin B has a molecular formula of C47H73NO17 and a molecular weight of 924.09.

The structure of amphotericin B is shown below:

MICROBIOLOGY

MECHANISM OF ACTION

Amphotericin B, the active ingredient of Am B isome, acts by binding to the sterol component of a cell membrane leading to alterations in cell permeability and cell death. While amphotericin B has a higher affinity for the ergosterol component of the fungal cell membrane, it can also bind to the cholesterol component of the mammalian cell leading to cytotoxicity. Am B isome, the liposomal preparation of amphotericin B, has been shown to penetrate the cell wall of both extracellular and intracellular forms of susceptible fungi.

ACTIVITY IN VITRO AND IN VIVO

Am B isome has shown in vitro activity comparable to amphotericin B against the following organisms: Aspergillus species (A. fumigatus, A. flavus), Candida species (C. albicans, C. krusei, C. lusitaniae, C. parapsilosis, C. tropicalis), Cryptococcus neoformans, and Blastomyces dermatitidis. However, standardized techniques for susceptibility testing of antifungal agents have not been established and results of such studies do not necessarily correlate with clinical outcome.

Am B isome is active in animal models against Aspergillus fumigatus, Candida albicans, Candida krusei, Candida lusitaniae, Cryptococcus neoformans, Blastomyces dermatitidis, Coccidioides immitis, Histoplasma capsulatum, Paracoccidioides brasiliensis, Leishmania donovani, and Leishmania infantum. The administration of Am B isome in these animal models demonstrated prolonged survival of infected animals, reduction of microorganisms from target organs, or a decrease in lung weight.

DRUG RESISTANCE

Mutants with decreased susceptibility to amphotericin B have been isolated from several fungal species after serial passage in culture media containing the drug, and from some patients receiving prolonged therapy. Drug combination studies in vitro and in vivo suggest that imidazoles may induce resistance to amphotericin B. However, the clinical relevance to drug resistance has not been established.

DESCRIPTION OF CLINICAL STUDIES

Eleven clinical studies supporting the efficacy and safety of Am B isome were conducted. This clinical program included both controlled and uncontrolled clinical studies. These studies, which involved 2171 patients, included patients with confirmed systemic mycoses, empirical therapy, and visceral leishmaniasis.

Nineteen hundred and forty-six episodes were evaluable for efficacy, of which 1280 (302 pediatric and 978 adults) were treated with Am B isome.

Three controlled empirical therapy trials compared the efficacy and safety of Am B isome to amphotericin B. One of these studies was conducted in a pediatric population, one in adults, and a third in patients aged 2 years or more. In addition, a controlled empirical therapy trial comparing the safety of Am B isome to Abelcet® (amphotericin B lipid complex) was conducted in patients aged 2 years or more.

One controlled trial compared the efficacy and safety of Am B isome to amphotericin B in HIV patients with cryptococcal meningitis.

One compassionate use study enrolled patients who had failed amphotericin B deoxycholate therapy or who were unable to receive amphotericin B deoxycholate because of renal insufficiency.

EMPIRICAL THERAPY IN FEBRILE NEUTROPENIC PATIENTS

Study 94-0-002, a randomized, double-blind, comparative multi-center trial, evaluated the efficacy of Am B isome (1.5-6 mg/kg/day) compared with amphotericin B deoxycholate (0.3-1.2 mg/kg/day) in the empirical treatment of 687 adult and pediatric neutropenic patients who were febrile despite having received at least 96 hours of broad spectrum antibacterial therapy. Therapeutic success required (a) resolution of fever during the neutropenic period, (b) absence of an emergent fungal infection, (c) patient survival for at least 7 days post therapy, (d) no discontinuation of therapy due to toxicity or lack of efficacy, and (e) resolution of any study-entry fungal infection.

The overall therapeutic success rates for Am B isome and amphotericin B deoxycholate were equivalent. Results are summarized in the following table. Note: The categories presented below are not mutually exclusive.

Empirical Therapy in Febrile Neutropenic Patients: Randomized, Double-Blind Study in 687 Patients
AmBisome Amphotericin B
Number of patients receiving at least
one dose of study drug
343 344
Overall Success 171 (49.9%) 169 (49.1%)
   Fever resolution during neutropenic period 199 (58%) 200 (58.1%)
   No treatment emergent fungal infection 300 (87.5%) 301 (87.7%)
   Survival through 7 days post study drug 318 (92.7%) 308 (89.5%)
   Study drug not prematurely discontinued
   due to toxicity or lack of efficacy *
294 (85.7%) 280 (81.4%)
* 8 and 10 patients, respectively, were treated as failures due to premature discontinuation alone.

This therapeutic equivalence had no apparent relationship to the use of prestudy antifungal prophylaxis or concomitant granulocytic colony stimulating factors.

The incidence of mycologically confirmed and clinically diagnosed, emergent fungal infections are presented in the following table. Am B isome and amphotericin B were found to be equivalent with respect to the total number of emergent fungal infections.

Empirical Therapy in Febrile Neutropenic Patients: Emergent Fungal Infections
AmBisome Amphotericin B
Number of patients receiving at least
one dose of study drug
343 344
   Mycologically confirmed fungal infection 11 (3.2%) 27 (7.8%)
   Clinically diagnosed fungal infection 32 (9.3%) 16 (4.7%)
   Total emergent fungal infections 43 (12.5%) 43 (12.5%)

Mycologically confirmed fungal infections at study-entry were cured in 8 of 11 patients in the Am B isome group and 7 of 10 in the amphotericin B group.

Study 97-0-034, a randomized, double-blind, comparative multi-center trial, evaluated the safety of Am B isome (3 and 5 mg/kg/day) compared with amphotericin B lipid complex (5 mg/kg/day) in the empirical treatment of 202 adult and 42 pediatric neutropenic patients. One hundred and sixty-six patients received Am B isome (85 patients received 3 mg/kg/day and 81 received 5 mg/kg/day) and 78 patients received amphotericin B lipid complex. The study patients were febrile despite having received at least 72 hours of broad spectrum antibacterial therapy. The primary endpoint of this study was safety. The study was not designed to draw statistically meaningful conclusions related to comparative efficacy, and in fact, Abelcet is not labeled for this indication.

Two supportive prospective randomized, open label, comparative multi-center studies examined the efficacy of two dosages of Am B isome (1 and 3 mg/kg/day) compared to amphotericin B deoxycholate (1 mg/kg/day) in the treatment of neutropenic patients with presumed fungal infections. These patients were undergoing chemotherapy as part of a bone marrow transplant or had hematological disease. Study 104-10 enrolled adult patients (n=134). Study 104-14 enrolled pediatric patients (n=214). Both studies support the efficacy equivalence of Am B isome and amphotericin B as empirical therapy in febrile neutropenic patients.

Treatment of Cryptococcal Meningitis in HIV Infected Patients

Study 94-0-013, a randomized, double-blind, comparative multi-center trial, evaluated the efficacy of Am B isome at doses (3 and 6 mg/kg/day) compared with amphotericin B deoxycholate (0.7 mg/kg/day) for the treatment of cryptococcal meningitis in 266 adult and one pediatric HIV positive patients (the pediatric patient received amphotericin B deoxycholate). Of the 267 treated patients, 86 received Am B isome 3 mg/kg/day, 94 received 6 mg/kg/day and 87 received amphotericin B deoxycholate; cryptococcal meningitis was documented by a positive CSF culture at baseline in 73, 85 and 76 patients, respectively. Patients received study drug once daily for an induction period of 11 to 21 days. Following induction, all patients were switched to oral fluconazole at 400 mg/day for adults and 200 mg/day for patients less than 13 years of age to complete 10 weeks of protocol-directed therapy. For mycologically evaluable patients, defined as all randomized patients who received at least one dose of study drug, had a positive baseline CSF culture, and had at least one follow-up culture, success was evaluated at week 2 (i.e., 14 ± 4 days), and was defined as CSF culture conversion. Success rates at 2 weeks for Am B isome and amphotericin B deoxycholate are summarized in the following table:

Success Rates at 2 weeks (CSF Culture Conversion) Study 94-0-013
AmBisome 3 mg/kg AmBisome 6 mg/kg Amphotericin B 0.7 mg/kg
Success at Week 2 35/60 (58.3%)
97.5% Cl 1 = -9.4%,
+ 31%
36/75
(48%) 97.5% Cl 1 =
-18.8%, + 19.8%
29/61 (47.5%)
197.5% Confidence Interval for the difference between Am B isome and amphotericin B success rates. A negative value is in favor of amphotericin B. A positive value is in favor of Am B isome.

Success at 10 weeks was defined as clinical success at week 10 plus CSF culture conversion at or prior to week 10. Success rates at 10 weeks in patients with positive baseline culture for cryptococcus species are summarized in the following table and show that the efficacy of Am B isome 6 mg/kg/day approximates the efficacy of the amphotericin B deoxycholate regimen. These data do not support the conclusion that Am B isome 3 mg/kg/day is comparable in efficacy to amphotericin B deoxycholate. The table also presents 10-week survival rates for patients treated in this study.

Success Rates and Survival Rates at week 10, Study 94-0-013 (see text for definitions)
AmBisome 3 mg/kg AmBisome 6 mg/kg Amphotericin B 0.7 mg/kg
Success in
patients with
documented
cryptococcal meningitis
27/73 (37%)
97.5% Cl 1 = -33.7%, + 2.4%
42/85 (49%)
97.5% Cl 1 = -20.9%, + 14.5%
40/76 (53%)
Survival rates 74/86 (86%)
97.5% Cl 1 = -13.8%, + 8.9%
85/94 (90%)
97.5% Cl 1 = -8.3%, + 12.2%
77/87 (89%)
197.5% Confidence Interval for the difference between Am B isome and amphotericin B success rates. A negative value is in favor of amphotericin B. A positive value is in favor of Am B isome.

The incidence of infusion-related, cardiovascular and renal adverse events was lower in patients receiving Am B isome compared to amphotericin B deoxycholate (see ADVERSE REACTIONS section for details), therefore, the risks and benefits (advantages and disadvantages) of the different amphotericin B formulations should be taken into consideration when selecting a patient treatment regimen.

Treatment of Patients with Aspergillus Species, Candida Species and/or Cryptococcus Species Infections Refractory to Amphotericin B Deoxycholate, or in Patients Where Renal Impairment or Unacceptable Toxicity Precludes the Use of Amphotericin B Deoxycholate

Am B isome was evaluated in a compassionate use study in hospitalized patients with systemic fungal infections. These patients either had fungal infections refractory to amphotericin B deoxycholate, were intolerant to the use of amphotericin B deoxycholate, or had pre-existing renal insufficiency. Patient recruitment involved 140 infectious episodes in 133 patients, with 53 episodes evaluable for mycological response and 91 episodes evaluable for clinical outcome. Clinical success and mycological eradication occurred in some patients with documented aspergillosis, candidiasis, and cryptococcis.

TREATMENT OF VISCERAL LEISHMANIASIS

Am B isome was studied in patients with visceral leishmaniasis who were infected in the Mediterranean basin with documented or presumed Leishmania infantum. Clinical studies have not provided conclusive data regarding efficacy against L. donovani and L. chagasi.

Am B isome achieved high rates of acute parasite clearance in immunocompetent patients when total doses of 12-30 mg/kg were administered. Most of these immunocompetent patients remained relapse-free during follow-up periods of 6 months or longer. While acute parasite clearance was achieved in most of the immunocompromised patients who received total doses of 30-40 mg/kg, the majority of these patients were observed to relapse in the 6 months following the completion of therapy. Of the 21 immunocompromised patients studied, 17 were coinfected with HIV; approximately half of the HIV infected patients had AIDS. The following table presents a comparison of efficacy rates among immunocompetent and immunocompromised patients infected in the Mediterranean basin who had no prior treatment or remote prior treatment for visceral leishmaniasis. Efficacy is expressed as both acute parasite clearance at the end of therapy (EOT) and as overall success (clearance with no relapse) during the follow-up period (F/U) of greater than 6 months for immunocompetent and immunocompromised patients:

AmBisome Efficacy in Visceral Leishmaniasis
Immunocompetent Patients
No. of Patients   
Parasite (%)
Clearance at EOT
  
Overall Success
(%) at F/U
87     86/87 (98.9) 83/86 (96.5)
Immunocompromised Patients
Regimen Total Dose Parasite (%)
Clearance at EOT
Overall Success
(%) at F/U
100 mg/day X 21 days 29-38.9 mg/kg 10/10 (100) 2/10 (20)
4 mg/kg/day, days 1-5,
and 10, 17, 24, 31, 38
40 mg/kg 8/9 (88.9) 0/7 (0)
TOTAL      18/19 (94.7) 2/17 (11.8)

When followed for 6 months or more after treatment, the overall success rate among immunocompetent patients was 96.5% and the overall success rate among immunocompromised patients was 11.8% due to relapse in the majority of patients. While case reports have suggested there may be a role for long-term therapy to prevent relapses in HIV coinfected patients (Lopez-Dupla, et al. J. Antimicrob Chemother 1993;32:657-659), there are no data to date documenting the efficacy or safety of repeat courses of Am B isome or of maintenance therapy with this drug among immunocompromised patients.

CLINICAL PHARMACOLOGY

PHARMACOKINETICS

The assay used to measure amphotericin B in the serum after administration of Am B isome does not distinguish amphotericin B that is complexed with the phospholipids of Am B isome from amphotericin B that is uncomplexed. The pharmacokinetic profile of amphotericin B after administration of Am B isome is based upon total serum concentrations of amphotericin B. The pharmacokinetic profile of amphotericin B was determined in febrile neutropenic cancer and bone marrow transplant patients who received 1-2 hour infusions of 1 to 5 mg/kg/day Am B isome for 3 to 20 days.

The pharmacokinetics of amphotericin B after administration of Am B isome are nonlinear such that there is a greater than proportional increase in serum concentrations with an increase in dose from 1 to 5 mg/kg/day. The pharmacokinetic parameters of total amphotericin B (mean ± SD) after the first dose and at steady state are shown in the table below.

Pharmacokinetic Parameters of AmBisome
Dose
(mg/kg/day):
1 2.5 5
Day 1
n = 8
Last
n = 7
1
n = 7
Last
n = 7
1
n = 12
Last
n = 9
Parameters         
Cmax
(mcg/mL)
7.3 ± 3.8 12.2 ± 4.9 17.2 ± 7.1 31.4 ± 17.8 57.6 ± 21 83 ± 35.2
AUC0-24
(mcg·hr/mL)
27 ± 14 60 ± 20 65 ± 33 197 ± 183 269 ± 96 555 ± 311
t½ (hr) 10.7 ± 6.4 7 ± 2.1 8.1 ± 2.3 6.3 ± 2 6.4 ± 2.1 6.8 ± 2.1
Vss(L/kg) 0.44 ± 0.27 0.14 ± 0.05 0.40 ± 0.37 0.16 ± 0.09 0.16 ± 0.10 0.10 ± 0.07
Cl (mL/hr/kg) 39 ± 22 17 ± 6 51 ± 44 22 ± 15 21 ± 14 11 ± 6

Distribution

Based on total amphotericin B concentrations measured within a dosing interval (24 hours) after administration of Am B isome, the mean half-life was 7-10 hours. However, based on total amphotericin B concentration measured up to 49 days after dosing Am B isome, the mean half-life was 100-153 hours. The long terminal elimination half-life is probably a slow redistribution from tissues. Steady state concentrations were generally achieved within 4 days of dosing.

Although variable, mean trough concentrations of amphotericin B remained relatively constant with repeated administration of the same dose over the range of 1 to 5 mg/kg/day, indicating no significant drug accumulation in the serum.

Metabolism

The metabolic pathways of amphotericin B after administration of Am B isome are not known.

Excretion

The mean clearance at steady state was independent of dose. The excretion of amphotericin B after administration of Am B isome has not been studied.

PHARMACOKINETICS IN SPECIAL POPULATIONS

Renal Impairment

The effect of renal impairment on the disposition of amphotericin B after administration of Am B isome has not been studied. However, Am B isome has been successfully administered to patients with pre-existing renal impairment (see DESCRIPTION OF CLINICAL STUDIES).

Hepatic Impairment

The effect of hepatic impairment on the disposition of amphotericin B after administration of Am B isome is not known.

Pediatric and Elderly Patients

The pharmacokinetics of amphotericin B after administration of Am B isome in pediatric and elderly patients have not been studied; however, Am B isome has been used in pediatric and elderly patients (see DESCRIPTION OF CLINICAL STUDIES).

Gender and Ethnicity

The effect of gender or ethnicity on the pharmacokinetics of amphotericin B after administration of Am B isome is not known.

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