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A Double-Blind Placebo-Controlled Study to Investigate the Action of Isoprinosine (Inosiplex) in Patients With Severe Acquired Immunodeficiency Syndrome
To evaluate the effect of Isoprinosine in patients diagnosed as having AIDS relative to: Laboratory (immunologic defects): * Comparison of total helper and suppressor T-cell numbers among the groups. * Comparison of changes in natural killer cell activity. * Comparison of other laboratory findings among the groups. Clinical changes: * Comparison of the frequency of opportunistic infections among the groups. * Comparison of the frequency of the development of AIDS-related malignancies. * Comparison of other clinical manifestations relative to severity and time of onset.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Newport Pharmaceuticals International Inc
Laguna Hills, California, United States
Last Updated
June 24, 2005
Inosine pranobex
DRUG
Lead Sponsor
Newport Pharmaceuticals International
NCT06694805
NCT04142047
Data Source & Attribution
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View ClinicalTrials.gov Terms and ConditionsNCT07428330