Viewing Study NCT00002155



Ignite Creation Date: 2024-05-05 @ 9:36 AM
Last Modification Date: 2024-10-26 @ 9:02 AM
Study NCT ID: NCT00002155
Status: COMPLETED
Last Update Posted: 2005-06-24
First Post: 1999-11-02

Brief Title: A Six-Month Safety and Antiviral Study in HIV-1 Seropositive AZT-Experienced Patients With CD4 Counts Less Than or Equal to 50 Cellsmm3 to Evaluate MK-639 Alone Versus Zidovudine AZT and 3TC Versus the Combination of MK-639 With AZT3TC
Sponsor: Merck Sharp Dohme LLC
Organization: NIH AIDS Clinical Trials Information Service

Study Overview

Official Title: A Six-Month Safety and Antiviral Study in HIV-1 Seropositive AZT-Experienced Patients With CD4 Counts Less Than or Equal to 50 Cellsmm3 to Evaluate MK-639 Alone Versus Zidovudine AZT and 3TC Versus the Combination of MK-639 With AZT3TC
Status: COMPLETED
Status Verified Date: 1996-06
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: To compare effects on CD4 counts and serum viral RNA among HIV-seropositive zidovudine AZT-experienced patients in three treatment arms indinavir sulfate MK-639 Crixivan plus AZT plus lamivudine 3TC versus MK-639 alone versus AZT3TC
Detailed Description: AZT-experienced patients are randomized to receive MK-639AZT3TC or MK-639 alone or AZT3TC Additionally patients who have received 6 months of AZT or who are intolerant but received prior 3TC or who require concomitant rifampin therapy may receive open-label MK-639

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
039 None None None