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| Sponsor: | National Institute of Allergy and Infectious Diseases (NIAID) |
|---|---|
| Information provided by: | National Institute of Allergy and Infectious Diseases (NIAID) |
| ClinicalTrials.gov Identifier: | NCT00000834 |
Purpose
To determine the safety and tolerance of methotrexate in HIV-infected patients. To determine the dose effective in modulating key markers of immune activation. To determine a dose suitable for Phase II or III evaluation in HIV-infected patients.
In HIV infection, complete immunological clearance of the foreign antigen does not occur, resulting in chronic immune activation. Because chronic immune activation may contribute to disease progression in HIV infection, immunomodulators may have therapeutic value in early HIV disease prior to development of opportunistic infections. The clinical benefits of methotrexate appear to derive from an anti-inflammatory effect; thus, it may reduce the state of chronic immune activation.
| Condition | Intervention | Phase |
|---|---|---|
|
HIV Infections |
Drug: Lamivudine Drug: Methotrexate Drug: Zidovudine |
Phase I |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety Study Primary Purpose: Treatment |
| Official Title: | A Phase I Study of Methotrexate for HIV Infection |
| Estimated Enrollment: | 30 |
In HIV infection, complete immunological clearance of the foreign antigen does not occur, resulting in chronic immune activation. Because chronic immune activation may contribute to disease progression in HIV infection, immunomodulators may have therapeutic value in early HIV disease prior to development of opportunistic infections. The clinical benefits of methotrexate appear to derive from an anti-inflammatory effect; thus, it may reduce the state of chronic immune activation.
Patients are randomized to receive methotrexate at Dose 1 or 2 (low doses) for 12 weeks, with 8 weeks of follow-up. If interim safety monitoring and viral burden results for the two cohorts support continuation, a third cohort of patients receive methotrexate starting at Dose 2 for the first 2 weeks, then at Dose 3 for the next 2 weeks, and at Dose 4 for the remaining 8 weeks, with 8 weeks of follow-up.
AS PER AMENDMENT 1/10/97:
The Dose 1 (the lowest dose) has been eliminated; the first 10 patients are now assigned to the next higher dose. Depending upon the results of interim safety data, the next cohort will be entered on the escalating dose regimen.
Also per this amendment, all patients will receive zidovudine and lamivudine for 30 days prior to the initiation of methotrexate, during the 12 weeks of methotrexate administration, and for the 8 weeks of follow-up.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria
Concurrent Medication:
Allowed:
PER AMENDMENT 5/15/96:
PER AMENDMENT 1/10/97:
Patients must have:
Exclusion Criteria
Co-existing Condition:
Patients with the following symptom or condition are excluded:
Concurrent Medication:
Excluded:
Concurrent Treatment:
AS PER AMENDMENT 1/10/97: Excluded:
Patients with the following prior conditions are excluded:
AS PER AMENDMENT 1/10/97:
Prior Medication:
Excluded:
Prior Treatment:
Excluded:
Contacts and Locations| United States, California | |
| Cedars Sinai Med Ctr | |
| Los Angeles, California, United States, 90048 | |
| United States, District of Columbia | |
| Georgetown Univ Med Ctr | |
| Washington, District of Columbia, United States, 20007 | |
| United States, Kansas | |
| Univ of Kansas School of Medicine | |
| Wichita, Kansas, United States, 67214 | |
| United States, Massachusetts | |
| New England Med Ctr | |
| Boston, Massachusetts, United States, 02111 | |
| United States, Michigan | |
| Harper Hosp | |
| Detroit, Michigan, United States, 48201 | |
| United States, New York | |
| Community Research Initiative on AIDS | |
| New York, New York, United States, 10001 | |
| United States, Texas | |
| Univ of Texas Southwestern Med Ctr of Dallas | |
| Dallas, Texas, United States, 75235 | |
| Study Chair: | Egorin M | |
| Study Chair: | Fox L |
More Information
| Study ID Numbers: | DATRI 013 |
| Study First Received: | November 2, 1999 |
| Last Updated: | August 20, 2008 |
| ClinicalTrials.gov Identifier: | NCT00000834 History of Changes |
| Health Authority: | United States: Federal Government |
|
Methotrexate Acquired Immunodeficiency Syndrome AIDS-Related Complex Zidovudine |
Lamivudine Disease Progression Anti-Inflammatory Agents Anti-HIV Agents |
|
Anti-Inflammatory Agents Antimetabolites Anti-Infective Agents Sexually Transmitted Diseases, Viral Slow Virus Diseases Antimetabolites, Antineoplastic Immunologic Factors Molecular Mechanisms of Pharmacological Action Antineoplastic Agents Physiological Effects of Drugs Zidovudine Lamivudine Reproductive Control Agents Reverse Transcriptase Inhibitors Anti-Retroviral Agents |
Therapeutic Uses Abortifacient Agents Methotrexate Dermatologic Agents Retroviridae Infections Nucleic Acid Synthesis Inhibitors RNA Virus Infections Anti-HIV Agents Immune System Diseases Acquired Immunodeficiency Syndrome Enzyme Inhibitors Folic Acid Antagonists Abortifacient Agents, Nonsteroidal Antiviral Agents Immunosuppressive Agents |