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Double-Blind Study of the Effect of Timunox (Thymopentin) on Lymphoproliferative Responses and Virus Load in HIV-Infected Subjects Receiving Nucleoside Analog Antiretroviral Therapy
To evaluate the mechanism whereby thymopentin appears to retard the progressive immune suppression attributable to HIV infection.
Patients are randomized to receive subcutaneous thymopentin or placebo thrice weekly for 4 weeks.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Dr Marcus Conant
San Francisco, California, United States
Dr Jeffrey Galpin
Tarzana, California, United States
Novum Inc
Pittsburgh, Pennsylvania, United States
Last Updated
June 24, 2005
60
Estimated participants
Thymopentin
DRUG
Lead Sponsor
Immunobiology Research Institute
NCT06694805
NCT04142047
Data Source & Attribution
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View ClinicalTrials.gov Terms and ConditionsNCT07428330