Official Title: “A Pilot Study of Fluconazole Plus Flucytosine for the Treatment of AIDS Patients With Acute Cryptococcal Meningitis.”

To evaluate and estimate the safety and efficacy of the combination of fluconazole and flucytosine as treatment for acute cryptococcal meningitis in patients with AIDS. Fluconazole and flucytosine have different mechanisms of action. Since fluconazole has not been associated with hematologic suppression and does not produce renal impairment that can result in higher serum flucytosine levels, this combination may be better tolerated than is amphotericin B plus flucytosine.

Study Type: Interventional

Study Design: Treatment, Randomized, Safety Study

Fluconazole and flucytosine have different mechanisms of action. Since fluconazole has not been associated with hematologic suppression and does not produce renal impairment that can result in higher serum flucytosine levels, this combination may be better tolerated than is amphotericin B plus flucytosine.

Patients in each cohort receive a lower dose of fluconazole alone or in combination with flucytosine, or a higher dose of fluconazole alone. Doses in subsequent cohorts are escalated if safety data in the previous cohort is satisfactory. Patients are evaluated weekly for the first 4 weeks and every 2 weeks thereafter. Therapy continues until 8 weeks after the CSF becomes culture negative, up to a maximum of 26 weeks.

Intervention(s) in this Clinical Trial

• Drug: Flucytosine
• Drug: Fluconazole

Inclusion Criteria

Concurrent Medication:

Allowed:

• Antiviral therapy (AZT, DHPG).
• Prophylaxis for Pneumocystis carinii pneumonia.
• Treatment for intercurrent opportunistic infection.

Concurrent Treatment:

Allowed:

• Radiation therapy for mucocutaneous Kaposi's sarcoma.

Patients must have:

• AIDS.
• Evidence of Cryptococcal neoformans in culture or lumbar CSF OR clinical and CSF findings compatible with cryptococcal meningitis.
• No evidence of acute or chronic meningitis of any etiology other than cryptococcosis.
• Life expectancy of at least 2 weeks.

Prior Medication:

Allowed:

• Prior antiviral therapy (AZT, DHPG).
• Prophylaxis for Pneumocystis carinii pneumonia.

Exclusion Criteria

Co-existing Condition:

Patients with the following symptoms or conditions are excluded:

• Relapsing on maintenance triazole therapy for cryptococcal meningitis.
• Unable to take oral medication.

Concurrent Medication:

Excluded:

• Concomitant use of any antifungal agent other than study drug.

Patients with the following prior conditions are excluded:

• History of allergy to or intolerance of imidazoles, azoles, or flucytosine.

Prior Medication:

Excluded:

• More than 1 mg/kg amphotericin B.
• Systemic antifungal agents within 7 days prior to study entry.

Gender Eligibility for this Clinical Trial: Both

Minimum Age for this Clinical Trial: 13 Years

Maximum Age for this Clinical Trial: N/A

Are Healthy Volunteers Accepted for this Clinical Trial?: No

Lead Sponsor: Pfizer

Information obtained from ClinicalTrials.gov on July 02, 2009

Link to the current ClinicalTrials.gov record. http://clinicaltrials.gov/show/NCT00002113

Study ID Number: 213A

ClinicalTrials.gov Identifier: NCT00002113

Health Authority: United States: Food and Drug Administration