A Comparison of Atovaquone and Pentamidine in the Prevention of Pneumocystis Carinii Pneumonia in HIV-Infected Patients Who Cannot Take TMP/SMX

Completed · Phase 3

Conditions studied: Pneumonia, Pneumocystis Carinii, HIV Infections

In brief

To assess whether high dose or low dose atovaquone suspension is more effective than aerosolized pentamidine as prophylaxis against Pneumocystis carinii pneumonia (PCP) in high-risk HIV-infected patients. To compare the safety of chronic administration of the three regimens in patients with advanced HIV disease. To determine the relationship between steady state atovaquone plasma concentrations and prophylactic efficacy against PCP.

Key facts

Study ID

NCT00002340

Run by

Glaxo Wellcome

People needed

615

Last updated by the study team

2005-06-24

Who can join

Age: 13 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Concurrent Medication:
• Allowed:
• Antimicrobial agents not specifically prohibited.
• Concurrent Treatment:
• Allowed:
• Transfusion.
• Patients must have:
• HIV positivity.
• Prior PCP (histologically confirmed) OR documented CD4 count < 200 cells/mm3 OR constitutional symptoms such as thrush or unexplained fever (> 100 F) for 2 or more weeks.
• No current or suspected active PCP, and no signs of active PCP on chest x-ray.
• Prior intolerance to TMP/SMX or other trimethoprim or sulfa-containing regimens.
• Life-expectancy of at least 6 months.
• NOTE:
• Pregnant women are eligible at the discretion of the investigator.

You may not qualify if…

• Co-existing Condition:
• Patients with the following symptoms or conditions are excluded:
• Significant psychosis or emotional disorder that would preclude study compliance.
• Severe chronic diarrhea (e.g., > five stools/day) that may negatively affect absorption of oral medication.
• Unable to take oral medication or unable or unwilling to take medication with food.
• Concurrent Medication:
• Excluded:
• Rifampin.
• Other investigational agents except for drugs available through Treatment INDs or expanded access programs.
• Medications likely to have anti-pneumocystis effect (e.g., dapsone, trimethoprim, pyrimethamine, trimetrexate, other DHFR inhibitors, sulfadiazine, sulfamethoxazole, other sulfonamides, primaquine, clindamycin, and sulfonylureas.
• Corticosteroids in greater than physiologic replacement doses for more than 21 consecutive days.
• Systemic therapy for CNS toxoplasmosis, Kaposi's sarcoma, lymphoma, other active malignancies, or other disease that may decrease life expectancy or confound assessment.
• Patients with the following prior conditions are excluded:
• History of severe or intractable intolerance to atovaquone or aerosolized pentamidine.
• Prior hypoglycemia, pancreatitis, arrhythmias, or severe hypotension associated with any form of pentamidine.
• Prior enrollment in this protocol. Active substance abuse that would preclude study compliance.

Where it is running

• Goodgame Med Group — Maitland, Florida, United States
• Bay Area AIDS Consortium — Tampa, Florida, United States
• Saint Vincent's Hosp and Med Ctr — New York, New York, United States
• Holmes Hosp — Cincinnati, Ohio, United States
• Hampton Roads Med Specialists — Hampton, Virginia, United States

Full record on ClinicalTrials.gov

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