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The Safety and Effectiveness of (+)-Calanolide A in HIV-Infected Patients Who Have Never Taken Anti-HIV Drugs

Phase 1
Conditions
HIV Infections
Registration Number
NCT00005120
Lead Sponsor
Sarawak MediChem Pharmaceuticals
Brief Summary

The purpose of this study is to see if it is safe and effective to give calanolide A to HIV-infected adults who have not used anti-HIV drugs in the past.

Detailed Description

Patients are randomized to receive (+)-calanolide A or placebo for 21 days. All patients may elect to receive an open-label, 3-month course of approved retroviral therapy (up to triple-drug therapy) to be selected by, and administered under the care of, the patients' physicians. If the patient has no insurance coverage or does not wish to utilize his/her insurance for anti-HIV medications, Sarawak MediChem Pharmaceuticals will provide these medications at no charge for up to 3 months.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
16
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (6)

South Florida Bioavailability Clinic

πŸ‡ΊπŸ‡Έ

Miami, Florida, United States

Chicago Ctr for Clinical Research

πŸ‡ΊπŸ‡Έ

Chicago, Illinois, United States

The CORE Ctr

πŸ‡ΊπŸ‡Έ

Chicago, Illinois, United States

Anderson Clinical Research

πŸ‡ΊπŸ‡Έ

Pittsburgh, Pennsylvania, United States

Burnside Clinic

πŸ‡ΊπŸ‡Έ

Columbia, South Carolina, United States

Univ of Texas Med Branch

πŸ‡ΊπŸ‡Έ

Galveston, Texas, United States

South Florida Bioavailability Clinic
πŸ‡ΊπŸ‡ΈMiami, Florida, United States

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