Clinical trial

TMC125-C206: A Phase III Study to Investigate the Efficacy, Tolerability and…

NCT00254046 · Tibotec Pharmaceuticals, Ireland, Industry · Completed

Key facts

NCT number NCT00254046
Title TMC125-C206: A Phase III Study to Investigate the Efficacy, Tolerability and Safety of TMC125 as Part of an Antiretroviral Regimen, Including TMC114/Ritonavir and an Investigator-selected Optimized Background, in HIV-1 Infected Patients With Limited to no Treatment Options.
Official title A Phase III Randomized, Double-blinded, Placebo-controlled Trial to Investigate the Efficacy, Tolerability and Safety of TMC125 as Part of an ART Regimen, Including TMC114/RTV and an Investigator-selected OBR, in HIV-1 Infected Patients With Limited Treatment to no Treatment Options.
Lead sponsor Tibotec Pharmaceuticals, Ireland, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions HIV
Intervention type Drug
Interventions TMC125, Placebo
Enrollment 616
Start date Nov 1, 2005
Primary completion Feb 1, 2007
Completion Jul 1, 2008
First posted Nov 15, 2005
Last update posted Jun 20, 2014
Countries Argentina, Brazil, Chile, Costa Rica, France, Mexico, Panama, Puerto Rico, Thailand, United States

At a glance

  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About ClinicalTrials.gov studies

ClinicalTrials.gov is the U.S. National Library of Medicine's registry of clinical studies conducted around the world. Contact and investigator details are not shown here.

Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

Browse all ClinicalTrials.gov studies