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A Study of Peldesine (BCX-34) in HIV-Infected Patients

Phase 1
Completed
Conditions
HIV Infections
Registration Number
NCT00002237
Lead Sponsor
BioCryst Pharmaceuticals
Brief Summary

The purpose of this study is to determine the highest amount of peldesine that is safe. This study will also see if this amount of peldesine is effective in lowering HIV levels in the blood.

Detailed Description

Patients are given either BCX-35 or placebo for 14 or 28 days. Plasma viral load will be determined at the MTD.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

Not provided

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Exclusion Criteria

Not provided

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Study & Design

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

Trial Locations

Locations (1)

Saint Francis Mem Hosp / HIV Care Unit

🇺🇸

San Francisco, California, United States

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