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| Sponsored by: |
National Institute of Allergy and Infectious Diseases (NIAID) |
| Information provided by: | National Institute of Allergy and Infectious Diseases (NIAID) |
| ClinicalTrials.gov Identifier: | NCT00001068 |
Purpose
To determine the influence of virus load, CD4 count, biologic phenotype, and presence of symptomatic disease on the response of HIV-infected patients to a new therapeutic regimen. PER AMENDMENT 8/27/96: To extend the availability of currently assigned ACTG 303 treatment for 6 months.
| Condition | Intervention | Phase |
|
HIV Infections |
Drug: Lamivudine |
Phase II |
| MedlinePlus related topics: | AIDS |
| Drug Information available for: | Zidovudine Lamivudine Didanosine Zalcitabine |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Placebo Control, Parallel Assignment, Efficacy Study |
| Official Title: | Influence of Risk Status for Disease Progression on the Response to Antiretroviral Interventions: A Follow-Up Study to ACTG 175 |
Eligibility
| Ages Eligible for Study: | 12 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria
Patients must have:
PER AMENDMENT 8/27/96:
Contacts and Locations![]() |
Show 59 Study Locations |
More Information
| Study ID Numbers: | ACTG 303 |
| First Received: | November 2, 1999 |
| Last Updated: | June 23, 2005 |
| ClinicalTrials.gov Identifier: | NCT00001068 |
| Health Authority: | United States: Federal Government |
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