Viewing Study NCT00002236



Ignite Creation Date: 2024-05-05 @ 11:07 AM
Last Modification Date: 2024-10-26 @ 9:02 AM
Study NCT ID: NCT00002236
Status: COMPLETED
Last Update Posted: 2005-06-24
First Post: 1999-11-02

Brief Title: A Study to Find the Best Dosing Schedule for Delavirdine Zidovudine and Indinavir in HIV-Positive Patients
Sponsor: Pharmacia and Upjohn
Organization: NIH AIDS Clinical Trials Information Service

Study Overview

Official Title: An Open-Label Parallel Group Pilot Study of Safety Tolerance Pharmacokinetics and Pharmacodynamics of BID and TID Regimens of Delavirdine Mesylate Zidovudine and Indinavir Sulfate in HIV-1 Infected Individuals
Status: COMPLETED
Status Verified Date: 2000-04
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 see whether it is better to take delavirdine DLV plus indinavir IDV plus zidovudine ZDV twice a day or three times a day
Detailed Description: Patients are divided into 2 treatment groups the groups are balanced with respect to viral load Group A receives ZDV DLV and IDV 3 times daily Group B receives ZDV DLV and IDV 2 times daily Patients are evaluated for changes from baseline in viral load and CD4 cell count

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
M33310072 None None None