A Phase I Study of Methotrexate for HIV Infection

NCT ID: NCT00000834

Last Updated: 2021-10-29

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Completion Date: 2002-06-30

Brief Summary

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.

Detailed Description

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.

Conditions

HIV Infections

Keywords

Methotrexate; Acquired Immunodeficiency Syndrome; AIDS-Related Complex; Zidovudine; Lamivudine; Disease Progression; Anti-Inflammatory Agents; Anti-HIV Agents

Study Design

• Allocation Method: RANDOMIZED
• Primary Study Purpose: TREATMENT

Interventions

Lamivudine

Intervention Type: DRUG

Methotrexate

Intervention Type: DRUG

Zidovudine

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

Concurrent Medication:

Allowed:

• Antiemetics and antidiarrheals.
• Acetaminophen.
• Oral hypoglycemic agents.

PER AMENDMENT 5/15/96:

• Stable dose of antiretroviral (must be stable for at least 1 month prior to study entry). [AS

PER AMENDMENT 1/10/97:

• Combination zidovudine/lamivudine or zidovudine alone.]

Patients must have:

• HIV seropositivity.
• CD4 count >= 300 cells/mm3.
• No AIDS-defining condition.

Exclusion Criteria

Co-existing Condition:

Patients with the following symptom or condition are excluded:

• Current positive PPD.

Concurrent Medication:

Excluded:

• Immunosuppressive or immunomodulatory drugs.
• Chronic nonsteroidal anti-inflammatory agents.
• Newly initiated antiretrovirals.
• Bone marrow suppressive drugs (e.g., TMP/SMX).

Concurrent Treatment:

AS PER AMENDMENT 1/10/97: Excluded:

• Antiretroviral therapy other than combination zidovudine/lamivudine or zidovudine alone; no initiation of other antiretroviral therapy should be planned while patient is on methotrexate.

Patients with the following prior conditions are excluded:

• Prior malignancies.
• Prior mucocutaneous herpes infection requiring antiviral therapy [AS PER AMENDMENT 7/31/96: Prior mucocutaneous herpes infection requiring systemic treatment with an antiviral agent (e.g., acyclovir); history of topical antiviral therapy is permitted].
• Anergic on DTH skin test within the past month (PER AMENDMENT 5/15/96: patients who are positive on DTH skin test but unable to receive the HIV-1 skin test because of allergies to insects, bee stings, etc., remain eligible for study enrollment).
• Inflammatory bowel disease, peptic ulcer disease, obesity combined with insulin-requiring diabetes, liver disease, or chronic renal disease within the past 6 months.
• Positive for HBsAg or hepatitis C antibody within the past 2 weeks.
• Chest radiograph within the past 60 days that shows cavity disease, infiltrates, or scars from prior disease that would preclude diagnosis of a new infectious process or drug-induced pneumonitis.

AS PER AMENDMENT 1/10/97:

• History of intolerance to zidovudine or lamivudine.

Prior Medication:

Excluded:

• Prior chemotherapy for malignancy.

Prior Treatment:

Excluded:

• Prior radiotherapy for malignancy. Alcohol abuse.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National Institute of Allergy and Infectious Diseases (NIAID)

NIH

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Egorin M

Role: STUDY_CHAIR

Fox L

Role: STUDY_CHAIR

Locations

Cedars Sinai Med Ctr

Los Angeles, California, United States

Georgetown Univ Med Ctr

Washington D.C., District of Columbia, United States

Univ of Kansas School of Medicine

Wichita, Kansas, United States

New England Med Ctr

Boston, Massachusetts, United States

Harper Hosp

Detroit, Michigan, United States

Community Research Initiative on AIDS

New York, New York, United States

Univ of Texas Southwestern Med Ctr of Dallas

Dallas, Texas, United States

Countries

United States

Other Identifiers

11742

Identifier Type: REGISTRY

Identifier Source: secondary_id

DATRI 013

Identifier Type: -

Identifier Source: org_study_id