PMPA Prodrug

A study of the safety and antiviral efficacy of the addition of PMPA Prodrug to combination antiretroviral regimens in treatment-experienced HIV-infected volunteers.

 

Background

PMPA is a new type of nucleotide reverse transcriptase inhibitor (NRTI) that has exhibited potent antiretroviral action. In earlier studies, greater than one log drops in plasma HIV levels were seen in the highest dose groups.
Objective
To determine whether PMPA is safe and effective as an antiretroviral agent.

 

Study Design

Volunteers are assigned to one of three dosing regimens of PMPA (75 mg, 150 mg or 300 mg, once daily) or placebo, in addition to their current antiretroviral therapy.

Inclusion
Criteria
  • HIV-positive male or female 18-65 y.o.
  • Viral load greater than 400 and 100,000 copies/mL
  • On stable antiretroviral therapy for at least 8 weeks prior to trial entry
  • Normal kidney and liver function

Status
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Enrollment completed; study ongoing
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For more information about this study, please call 310/358.2429 or e-mail Corie Castro at ccastro@aidsresearch.org

We encourage participation by women and people of color.

This ad was reviewed and approved by the AIDS Research Alliance Institutional Review Board in January, 2001.

 


 

 

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