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A Study to Evaluate the Safety and Effectiveness of a New Non-Nucleoside Reverse Transcriptase Inhibitor (NNRTI), (+)-Calanolide A, in HIV-Positive Patients Who Have Never Received Anti-HIV Treatment

Phase 1
Completed
Conditions
HIV Infections
Registration Number
NCT00002243
Lead Sponsor
Sarawak MediChem Pharmaceuticals
Brief Summary

The purpose of this study is to test the safety and effectiveness of a new non-nucleoside reverse transcriptase inhibitor (NNRTI), (+)-calanolide A, in HIV-positive patients who have never received anti-HIV treatment.

Detailed Description

Patients are randomized into 2 cohorts, with Cohort 2 receiving a higher dosage than Cohort 1. Patients in each cohort receive either (+)-calanolide A or a placebo for 14 days, followed by a 14-day follow-up period. Following study treatment, patients may elect to receive an open-label, 6-month course of anti-HIV drugs to be selected by and administered under the care of the patient's physician.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
32
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 (9)

Anderson Clinical Research / Inc

🇺🇸

Pittsburgh, Pennsylvania, United States

Univ of Texas / Med Branch at Galveston

🇺🇸

Galveston, Texas, United States

Univ of Maryland Institute of Human Virology

🇺🇸

Baltimore, Maryland, United States

Boston Med Ctr / Clinical Research Office

🇺🇸

Boston, Massachusetts, United States

South Florida Bioavailability Clinic

🇺🇸

Miami, Florida, United States

Cook County Hosp

🇺🇸

Chicago, Illinois, United States

Treasure Coast Infectious Disease Consultants

🇺🇸

Vero Beach, Florida, United States

Beth Israel Med Ctr

🇺🇸

New York, New York, United States

Vanderbilt Univ Med Ctr

🇺🇸

Nashville, Tennessee, United States

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