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Clinical Trial Summary

The primary objective of the study is to determine if Serostim® 4 mg administered daily for 12 weeks as treatment for the abnormal fat accumulation and distribution associated with HIV-associated Adipose Redistribution Syndrome (HARS) reduces Visceral Adipose Tissue (VAT, measured by CT scan) more effectively than placebo.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00082628
Study type Interventional
Source EMD Serono
Contact
Status Completed
Phase Phase 3
Start date May 28, 2004
Completion date September 28, 2005

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