Viewing Study NCT00116415



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Study NCT ID: NCT00116415
Status: COMPLETED
Last Update Posted: 2011-04-22
First Post: 2005-06-29

Brief Title: DART I - A Phase IV Study of 3 Antiretroviral Medicines in Combination in HIV Patients Who Have Not Been Previously Treated With Antiretroviral Therapy
Sponsor: Bristol-Myers Squibb
Organization: Bristol-Myers Squibb

Study Overview

Official Title: Daily Antiretroviral Therapy DART 1 An Open-Label Single-Arm Prospective Multicenter Clinical Trial to Evaluate the Efficacy and Safety of Didanosine Enteric Coated Ddl-EC in Combination With Lamivudine 3TC and Efavirenz EFV Once Daily in Anti-Retroviral Therapy ART Naive HIV-Infected Patients
Status: COMPLETED
Status Verified Date: 2011-04
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 evaluate whether a therapy with an all once daily regimen of efavirenz EFV didanosine ddI-EC and lamivudine 3TC leads to improved outcomes as measured by viral load CD4 counts adherence safety and tolerability
Detailed Description: None

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