Viewing Study NCT00051038



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Last Modification Date: 2024-10-26 @ 9:08 AM
Study NCT ID: NCT00051038
Status: COMPLETED
Last Update Posted: 2011-04-14
First Post: 2002-12-31

Brief Title: Study of Adding Entecavir to Current Lamivudine Therapy in HIV and HBV Co-Infected Patients
Sponsor: Bristol-Myers Squibb
Organization: Bristol-Myers Squibb

Study Overview

Official Title: A Phase II Study of the Safety and Efficacy of Adding Entecavir to Current Lamivudine Therapy in HIV and HBV Co-Infected Patients Who Have Hepatitis B Viremia While Being Treated With Lamivudine
Status: COMPLETED
Status Verified Date: 2007-08
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 clinical research study is to assess the safety and effectiveness of entecavir when being added to lamivudine in the treatment of adults with chronic hepatitis B infection who are co-infected with HIV
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