Clinical trial

A Study to Evaluate the Safety and Efficacy of Adding Enfuvirtide to Oral Highly…

NCT00487188 · Hoffmann-La Roche, Industry · Completed

Key facts

NCT number NCT00487188
Title A Study to Evaluate the Safety and Efficacy of Adding Enfuvirtide to Oral Highly Active Antiretroviral Therapy (HAART) in Human Immunodeficiency Virus (HIV) Patients With Prior Treatment Experience
Official title Phase IIIb/IV Randomized, Controlled Study Evaluating an Intensification Treatment Strategy of Adding Enfuvirtide (ENF) to an Oral Highly Active AntiRetroviral Therapy (HAART) in Treatment Experienced Patients
Acronym INTENSE
Lead sponsor Hoffmann-La Roche, Industry
Status Completed
Phase Phase 4
Study type Interventional
Conditions HIV Infections
Intervention type Drug
Interventions Enfuvirtide, Highly active antiretroviral treatment (HAART)
Enrollment 47
Start date Nov 1, 2005
Primary completion Nov 1, 2007
Completion Apr 1, 2008
First posted Jun 15, 2007
Last update posted Aug 13, 2015
Countries Canada, France, Germany, Israel, Italy, Mexico, Netherlands, Spain, Switzerland, United States

At a glance

  • Yes Results posted
  • None Linked FDA submissions

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

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

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