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A Study of Timunox (Thymopentin) in HIV-Infected Patients Receiving Other Anti-HIV Drugs

Phase 2
Completed
Conditions
HIV Infections
Registration Number
NCT00002332
Lead Sponsor
Immunobiology Research Institute
Brief Summary

To evaluate the mechanism whereby thymopentin appears to retard the progressive immune suppression attributable to HIV infection.

Detailed Description

Patients are randomized to receive subcutaneous thymopentin or placebo thrice weekly for 4 weeks.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (3)

Dr Jeffrey Galpin

🇺🇸

Tarzana, California, United States

Dr Marcus Conant

🇺🇸

San Francisco, California, United States

Novum Inc

🇺🇸

Pittsburgh, Pennsylvania, United States

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