Pentoxifylline (Trental) as a Modulator of Tumor Necrosis Factor and of HIV Replication in Patients With AIDS

Inclusion Criteria

Concurrent Medication:

Required:

• Zidovudine (AZT), didanosine (ddI), dideoxycytidine (ddC), or a combination thereof, at current dosage for the 8 weeks of study treatment.
• Prophylaxis (e.g., aerosolized pentamidine, trimethoprim / sulfamethoxazole (TMP / SMX), dapsone for Pneumocystis carinii pneumonia (PCP) if CD4 cell count is < 200 cells/mm3

Allowed:

• Concurrent maintenance therapy for opportunistic infections.

Prior Medication: Required:

• Zidovudine (AZT), didanosine (ddI), dideoxycytidine (ddC), or a combination thereof, for at least 2 months.

Patients must have the following:

• Diagnosis of AIDS.
• Documented HIV seropositivity.
• Ability to give informed consent and willingness to comply with visit schedule and all procedures.

Exclusion Criteria

Co-existing Condition:

Patients with the following conditions or symptoms are excluded:

• Lymphoma or visceral Kaposi's sarcoma.
• Active peptic ulcer or bleeding disorder.
• Hemophilia. Known intolerance to pentoxifylline, theophylline, or caffeine.

Concurrent Medication:

Excluded:

• Warfarin and heparin.
• Biological response modifiers (e.g., erythropoietin, interferon, G-CSF, GM-CSF).

Cytotoxic chemotherapy.

• Megestrol acetate. Corticosteroids.

Concurrent Treatment:

Excluded:

• Radiation therapy. Blood products or transfusions.

Patients with the following are excluded:

• Presence of an active opportunistic infection.
• Major surgery within 30 days of study treatment.

Prior Medication:

Excluded:

• Biological response modifiers (including interferon, interleukin), corticosteroids, or megestrol acetate within 14 days of first (screening) TNF level.
• Erythropoietin dependency or within 30 days of study treatment.

Prior Treatment:

Excluded:

• Transfusion or blood product dependency or use within 30 days of study treatment.

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety