Open, Non-Comparative Study of Fluconazole in Patients With Coccidioidal Meningitis

HIV Infections Clinical Trial

Official title:

Open, Non-Comparative Study of Fluconazole in Patients With Coccidioidal Meningitis

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00002010
• Other study ID #: 012P
• Secondary ID: 056-170
• Status: Completed
• Phase: N/A
• First received: November 2, 1999
• Last updated: June 23, 2005

Study information

• Verified date: February 1992
• Source: NIH AIDS Clinical Trials Information Service
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The study is intended to examine the efficacy of fluconazole for the treatment of coccidioidal meningitis in patients with new onset of infection, relapse of previous infection, or failed previous therapy. Drug efficacy, safety and tolerance will be examined.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 0
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 13 Years and older

Eligibility

Inclusion Criteria

Concurrent Medication:

Allowed:

• Immunosuppressive therapy including corticosteroids and/or cytotoxic agents.

• Antiviral therapy (e.g., zidovudine (AZT)).

• Prophylaxis for Pneumocystis carinii pneumonia (PCP).

• Any exceptions to use of concomitant medications must be approved by Pfizer Central Research prior to study entry.

Concurrent Treatment:

Allowed:

• Radiation therapy for mucocutaneous Kaposi's sarcoma.

Patients must:

• Be clinically judged to be in need of treatment for coccidioidal meningitis.

• Have > 1 week life expectancy.

• Allowed:

• Immunocompromised patients.

• Patients with renal disease will have the dose of fluconazole adjusted and serum levels may be monitored.

Prior Medication:

Allowed:

• Amphotericin B.

• Ketoconazole.

• Miconazole.

Exclusion Criteria

Co-existing Condition:

Patients with the following conditions or symptoms are excluded:

• Current antifungal infection that is responding to another agent. Findings of improvement include one of the following, while on other therapy (without subsequent relapse of the item):

• CSF culture conversion from positive to negative.

• OR

• CSF antibody titer decrease of at least one dilution.

• OR

• Improvement in signs and symptoms of meningitis.

• Have received more than minimal systemic antifungal therapy (see Patient Inclusion Criteria), unless they meet criteria for previous treatment failure or relapse. They must not have received this therapy since the time relapse or failure was documented, except for minimal antifungal therapy allowed in Patient Inclusion Criteria.

• Immediately life-threatening coccidioidomycosis defined as infection of such a degree of clinical severity that the patient would be expected to die within 1 week, if untreated, based on clinical judgment.

• Experienced a prior allergic reaction or major side effect from an imidazole or triazole compound.

Concurrent Medication:

Excluded:

• Barbiturates.

• Phenytoin.

• Oral hypoglycemics.

• Coumadin type anticoagulants.

• Other systemic or intrathecal antifungal therapy.

• Other experimental agents with exceptions noted in concomitant medications section.

• Any exceptions to these prohibitions of concomitant medications must be approved by Pfizer Central Research prior to study entry.

Patients with the following are excluded:

• Are responding or are improving on current antifungal therapy with another agent.

• Have received more than minimal systemic antifungal therapy (see Patient Inclusion Criteria), unless they meet criteria for previous treatment failure or relapse. They must not have received this therapy since the time relapse or failure was documented, except for minimal antifungal therapy allowed in Patient Inclusion Criteria.

• Immediately life-threatening coccidioidomycosis defined as infection of such a degree of clinical severity that the patient would be expected to die within 1 week, if untreated, based on clinical judgment.

• Experienced a prior allergic reaction or major side effect from an imidazole or triazole compound.

Study Design

Endpoint Classification: Safety Study, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• HIV Infections
• Meningitis
• Meningitis, Fungal

Intervention

Drug:
• Fluconazole

Locations

Country	Name	City	State
United States	Audie L Murphy Veterans Administration Hosp	San Antonio	Texas
United States	HIV Research Group	San Diego	California
United States	Tucson Veterans Administration Med Ctr	Tucson	Arizona

Sponsors (1)

Lead Sponsor	Collaborator
Pfizer

Country where clinical trial is conducted

United States,