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A Study to Evaluate CJC 1295 in HIV Patients With Visceral Obesity

2014-08-27 03:47:05 | BioPortfolio

Summary

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.

Study Design

Allocation: Randomized, Control: Placebo Control, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Conditions

Obesity

Intervention

CJC 1295

Status

Terminated

Source

ConjuChem

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:47:05-0400

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