Viewing Study NCT00294372



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Last Modification Date: 2024-10-26 @ 9:23 AM
Study NCT ID: NCT00294372
Status: TERMINATED
Last Update Posted: 2013-11-14
First Post: 2006-02-20

Brief Title: Phase II Study on the Antiviral Activity and Safety of BILR 355 BS in HIV-1 Infected NNRTI-treated Patients
Sponsor: Boehringer Ingelheim
Organization: Boehringer Ingelheim

Study Overview

Official Title: Randomised Double-blind Placebo-controlled 7 Day Monotherapy Phase IIa Study to Evaluate the Antiviral Activity and Safety of Increasing Doses of Oral Administered RTV-boosted BILR 355 BS 75 mg and 150 mg Twice Daily in HIV-1-infected NNRTI-experienced Patients Followed by 28 Day Combination Therapy With Tipranavir or Lopinavir Based HAART-regimen
Status: TERMINATED
Status Verified Date: 2013-11
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 general aim is to evaluate the antiviral activity and safety of increasing doses of oral administered RTV-boosted BILR 355 BS 75 mg and 150 mg twice daily in HIV-1-infected NNRTI-experienced patients followed by 28 day combination therapy with Tipranavir or Lopinavir based HAART-regimen
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