A Study to Evaluate CJC 1295 in HIV Patients With Visceral Obesity
|ClinicalTrials.gov Identifier: NCT00267527|
Recruitment Status : Terminated
First Posted : December 21, 2005
Last Update Posted : October 16, 2006
This is a multicenter, randomized, placebo-controlled, double-blind, Phase 2 study. Patients will be treated for a total of 12 weeks. There will be a 6 week follow-up period after the treatment period ends. Patients will be randomly assigned to low dose CJC 1295, high dose CJC 1295 or placebo.
The objective is to assess and compare the efficacy, pharmacokinetics, safety, and tolerability of CJC 1295 in patients with human immunodeficiency virus (HIV) associated visceral obesity.
|Condition or disease||Intervention/treatment||Phase|
|Obesity HIV Infections||Drug: CJC 1295||Phase 2|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||120 participants|
|Intervention Model:||Parallel Assignment|
|Official Title:||A Multicenter, Randomized, Placebo-Controlled, Double-Blind, Phase 2 Study to Evaluate the Efficacy and Safety of CJC 1295 Administered for 12 Weeks in HIV Infected Patients With HIV Associated Visceral Obesity|
|Study Start Date :||December 2005|
|Estimated Study Completion Date :||September 2006|