Viewing Study NCT00002237



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Last Modification Date: 2024-10-26 @ 9:02 AM
Study NCT ID: NCT00002237
Status: COMPLETED
Last Update Posted: 2005-06-24
First Post: 1999-11-02

Brief Title: A Study of Peldesine BCX-34 in HIV-Infected Patients
Sponsor: BioCryst Pharmaceuticals
Organization: NIH AIDS Clinical Trials Information Service

Study Overview

Official Title: Phase I Placebo-Controlled Study of Oral BCX-34 Peldesine in HIV-Infected Patients
Status: COMPLETED
Status Verified Date: 1999-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
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

Study Oversight

Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?:
Secondary IDs
Secondary ID Type Domain Link
96-009 None None None