Viewing Study NCT00013897



Ignite Creation Date: 2024-05-05 @ 11:23 AM
Last Modification Date: 2024-10-26 @ 9:06 AM
Study NCT ID: NCT00013897
Status: COMPLETED
Last Update Posted: 2011-05-04
First Post: 2001-03-31

Brief Title: A Comparison of BMS-232632 With Efavirenz Each in Combination With Zidovudine-Lamivudine
Sponsor: Bristol-Myers Squibb
Organization: Bristol-Myers Squibb

Study Overview

Official Title: A Phase III Study Comparing the Antiviral Efficacy and Safety of BMS-232632 With Efavirenz Each in Combination With Fixed Dose Zidovudine-Lamivudine
Status: COMPLETED
Status Verified Date: 2011-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to compare the effectiveness of treatment with BMS-232632 to that of efavirenz EFV when both are used with zidovudine ZDV and lamivudine 3TC
Detailed Description: This is a multinational 2-arm study Patients in 1 arm receive BMS-232632 plus EFV placebo capsules Patients in the other arm receive EFV plus BMS-232632 placebo Both arms also receive a fixed dose of ZDV-3TC

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
AI424-034 None None None