Viewing Study NCT00004584



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Last Modification Date: 2024-10-26 @ 9:04 AM
Study NCT ID: NCT00004584
Status: COMPLETED
Last Update Posted: 2011-05-04
First Post: 2000-02-10

Brief Title: Safety and Effectiveness of a New Protease Inhibitor BMS-232632 in HIV-Positive Patients Who Have Received Previous Treatment
Sponsor: Bristol-Myers Squibb
Organization: Bristol-Myers Squibb

Study Overview

Official Title: Safety and Antiviral Efficacy of a Novel HIV-1 Protease Inhibitor BMS-232632 in Combination Regimens as Compared to a Reference Combination Regimens in Antiretroviral-Experienced HIV-Infected Subjects
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 look at the safety and effectiveness of an experimental protease inhibitor a type of anti-HIV drug called BMS-232632 Doctors will compare an anti-HIV drug combination that includes BMS-232632 to a drug combination that includes ritonavir
Detailed Description: This is a three-arm study patients are randomized to receive BMS-232632 at two different doses or RTV in combination with SQV and two nucleoside analogues over 48 weeks Randomization is stratified for baseline phenotypic sensitivity

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
AI424-009 None None None