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Search / Trial NCT00000708

Multi-center Comparison of Fluconazole (UK-49,858) and Amphotericin B as Treatment for Acute Cryptococcal Meningitis

Launched by NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES (NIAID) · Aug 30, 2001

Trial Information

Current as of March 22, 2025

Completed

Keywords

Aids Related Opportunistic Infections Meningitis Injections, Intravenous Cryptococcus Neoformans Cryptococcosis Drug Therapy, Combination Fluconazole Administration, Oral Acquired Immunodeficiency Syndrome Amphotericin B

ClinConnect Summary

Cryptococcal meningitis is an important cause of disease and death among patients with AIDS. Usually AMB is given either alone or with FLC to patients with this infection, but these treatments are not always effective and both have toxic effects. Animal studies and preliminary studies in humans show that FCZ is active in cryptococcal meningitis and suggest that it may be less toxic than either AMB or FLC.

Patients accepted into the study are randomly assigned to FCZ or AMB. Patients assigned to FCZ take FCZ by mouth daily for 10 weeks. Patients assigned to AMB are given intravenous injecti...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria
  • Concurrent Medication:
  • Allowed:
  • Immunosuppressant therapy.
  • Cyclosporin plasma concentrations should be monitored and appropriate dosage adjustments made when used with amphotericin B or fluconazole.
  • Antiviral therapy.
  • Prophylaxis for Pneumocystis carinii pneumonia.
  • Treatment of intercurrent opportunistic infection as long as no investigational agent, or approved agent for an investigational indication, is used.
  • Antipyretics, hydrocortisone, or meperidine to prevent or ameliorate side effects associated with amphotericin B.
  • Concurrent Treatment:
  • Allowed:
  • - Radiation therapy for mucocutaneous Kaposi's sarcoma.
  • Patients must have:
  • Written informed consent obtained from the patient or from the patient's legal guardian.
  • * One of the following:
  • * (1) Tentative identification of Cryptococcus neoformans in culture of lumbar cerebrospinal fluid (CSF). Results of baseline cultures need not be available when therapy is begun, but therapy is discontinued if the baseline CSF culture is later found to be negative for C. neoformans, or (2) Clinical and CSF findings (cell count, protein, glucose) compatible with cryptococcal meningitis plus one of the following:
  • (a) Positive CSF India ink examination, (b) Culture or biopsy evidence of extraneural cryptococcal infection, (c) Positive serum of CSF cryptococcal antigen test, or increase in titer for previously treated patients with suspected relapse, or (d) Biopsy evidence of central nervous system cryptococcal infection.
  • Treatment status of either no prior systemic antifungal therapy for cryptococcosis or relapse after prior therapy. The success of prior therapy must have been documented by negative CSF culture at the end of therapy.
  • Prior Medication:
  • Allowed within 4 weeks of study entry:
  • - Successful prior therapy for cryptococcosis, but no more than 1 mg/kg/week amphotericin B.
  • Allowed:
  • Immunosuppressant therapy.
  • Antiviral therapy.
  • Prophylaxis for Pneumocystis carinii pneumonia.
  • Exclusion Criteria
  • Co-existing Condition:
  • Excluded:
  • Acute or chronic meningitis based on any etiology other than cryptococcosis.
  • History of allergy to or intolerance of imidazoles, or amphotericin B.
  • * Moderate or severe liver disease defined as any one or more of the following:
  • SGOT or SGPT \> 5 x upper limit of normal, total bilirubin \> 2.5 mg/dl, prothrombin time \> 5 seconds over control, or alkaline phosphatase \> 2 x upper limit of normal.
  • Comatose patients.
  • Concurrent Medication:
  • Excluded:
  • Drugs with low therapeutic ratios that undergo hepatic metabolism may not be used with fluconazole until possible drug interactions have been clarified.
  • Coumarin-type anticoagulants.
  • Oral hypoglycemics.
  • Barbiturates.
  • Immunostimulants.
  • Investigational drugs or approved (licensed) drugs for investigational indications.
  • Systemic antifungal agent other than the assigned study drug.
  • Concurrent Treatment:
  • Excluded:
  • Lymphocyte replacement.
  • Prior Medication:
  • Excluded within 4 weeks of study entry:
  • More than 1 mg/kg/week amphotericin B.
  • Patients unlikely to survive more than 2 weeks.

Trial Officials

Armstrong D

Study Chair

About National Institute Of Allergy And Infectious Diseases (Niaid)

The National Institute of Allergy and Infectious Diseases (NIAID) is a key component of the National Institutes of Health (NIH) dedicated to advancing the understanding, prevention, and treatment of infectious and immune-mediated diseases. Through rigorous clinical trials, NIAID aims to foster innovative research that enhances public health and addresses global health challenges, including emerging infectious diseases and allergies. The institute collaborates with various partners, including academic institutions, industry, and international organizations, to translate scientific discoveries into effective therapies and vaccines. NIAID's commitment to high-quality clinical research is integral to improving health outcomes and informing policy decisions in the realm of infectious diseases and immunology.

Locations

West Columbia, South Carolina, United States

Chapel Hill, North Carolina, United States

Miami, Florida, United States

Bronx, New York, United States

New Orleans, Louisiana, United States

New York, New York, United States

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Discussion 0

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