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| Sponsored by: |
Research Institute for Genetic and Human Therapy |
| Information provided by: | NIH AIDS Clinical Trials Information Service |
| ClinicalTrials.gov Identifier: | NCT00002427 |
Purpose
The purpose of this study is to compare the safety and effectiveness of 9 doses of HU in order to find the best dose of HU to use with ddI and d4T in fighting HIV infection.
HU plus ddI plus d4T appears to be a suitable anti-HIV drug combination for long-term control of HIV. This combination can sharply decrease viral load (level of HIV in the body) with few side effects, making it easy to take.
| Condition | Intervention | Phase |
|
HIV Infections |
Drug: Hydroxyurea Drug: Stavudine Drug: Didanosine |
Phase I |
| MedlinePlus related topics: | AIDS AIDS Medicines |
| Drug Information available for: | Didanosine Stavudine Hydroxyurea |
| Study Type: | Interventional |
| Study Design: | Treatment, Factorial Assignment, Safety Study |
| Official Title: | A Phase I/II Study of the Safety and Antiretroviral Activity of Nine Hydroxyurea Regimens in Combination With ddI and d4T in Subjects With HIV Infection |
| Estimated Enrollment: | 225 |
| Study Start Date: | May 1999 |
The combination of HU plus ddI plus d4T appears to be suitable for long-term control of HIV in that it: (1) has a novel resistance/rebound profile demonstrating virus suppression even in the presence of ddI-resistant mutants; (2) can produce a pronounced fall in viral load; and (3) is well tolerated (over 200 patients have been treated for up to 3 years with minimal side effects).
Patients are stratified by antiretroviral experience: naive (no more than 2 weeks of therapy) versus experienced (more than 2 weeks). Patients must discontinue all antiretroviral therapy for at least 28 days prior to randomization to 1 of 9 HU treatment arms. Treatment arms are divided into 3 HU dose categories: very low, low, and medium. Within each category HU is administered daily on 3 different dosing schedules. Depending on viral load, patients on the very low and low dose arms may have the opportunity to intensify their HU dose at any time beyond Week 12, provided no Grade 3 or 4 HU-related toxicity is present (these patients are monitored for an additional 8 weeks following intensification). All patients receive ddI and d4T at the same doses every day. When 50% of patients have completed 24 weeks of treatment, an analysis is made to determine whether or not to continue the 52-week study without modifications. Patients are monitored periodically for changes in plasma HIV RNA, CD4 cell counts, weight, and symptoms.
Eligibility
| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria
Patients may be eligible for this study if they:
Exclusion Criteria
Patients will not be eligible for this study if they:
Contacts and Locations| United States, California | |||||
| AIDS Healthcare Foundation | |||||
| Los Angeles, California, United States, 90027 | |||||
| San Francisco VA Med Ctr | |||||
| San Francisco, California, United States, 94121 | |||||
| United States, Connecticut | |||||
| Gary Blick MD | |||||
| Stamford, Connecticut, United States, 06901 | |||||
| United States, District of Columbia | |||||
| Dr Bruce Rashbaum | |||||
| Washington, District of Columbia, United States, 20037 | |||||
| United States, Florida | |||||
| IDC Research Initiative | |||||
| Altamonte Springs, Florida, United States, 32701 | |||||
| Boulevard Comprehensive Care Ctr | |||||
| Jacksonville, Florida, United States, 32209 | |||||
| Center for Quality Care | |||||
| Tampa, Florida, United States, 33609 | |||||
| United States, Georgia | |||||
| AIDS Research Consortium of Atlanta Inc | |||||
| Atlanta, Georgia, United States, 30308 | |||||
| United States, Massachusetts | |||||
| New England Med Ctr | |||||
| Boston, Massachusetts, United States, 02111 | |||||
| United States, New York | |||||
| Albany Med College | |||||
| Albany, New York, United States, 122083479 | |||||
| Mt Vernon Hosp | |||||
| Mt. Vernon, New York, United States, 10550 | |||||
| United States, Pennsylvania | |||||
| Univ of Pennsylvania Med Ctr | |||||
| Philadelphia, Pennsylvania, United States, 19104 | |||||
| Thomas Jefferson Univ | |||||
| Philadelphia, Pennsylvania, United States, 19107 | |||||
| United States, South Carolina | |||||
| Coastal Carolina Research Ctr | |||||
| Mount Pleasant, South Carolina, United States, 29464 | |||||
| United States, Texas | |||||
| Univ of Texas Southwestern Med Ctr of Dallas | |||||
| Dallas, Texas, United States, 75235 | |||||
| Univ of Texas Med Branch | |||||
| Galveston, Texas, United States, 775550835 | |||||
| Montrose Clinic | |||||
| Houston, Texas, United States, 77006 | |||||
| United States, Washington | |||||
| Swedish Med Ctr | |||||
| Seattle, Washington, United States, 98122 | |||||
| Research Institute for Genetic and Human Therapy |
| Study Chair: | Franco Lori | |
| Study Chair: | Julianna Lisziewicz |
More Information
| Study ID Numbers: | 304A, RIGHT 702 |
| First Received: | November 2, 1999 |
| Last Updated: | June 23, 2005 |
| ClinicalTrials.gov Identifier: | NCT00002427 |
| Health Authority: | United States: Food and Drug Administration |
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