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DSMB RECOMMENDS THAT ALL CLINICAL STUDIES IN MARAVIROC PHASE 3 DEVELOPMENT PROGRAM CONTINUE WITHOUT CHANGE
 
 
  May 4, 2006 Studies fully enrolled with patient volunteers
 
Pfizer reported that the independent Data Safety Monitoring Board (DSMB) for maraviroc, Pfizerfs CCR5 antagonist in development for the treatment of HIV, met in April 2006 as part of their scheduled review of the phase 2b/3 development program. The maraviroc DSMB is an independent group that includes experts who specialize in the treatment of patients with HIV/AIDS. The ongoing review of data by the DSMB helps to ensure the safety of patients participating in the studies.
 
The clinical development program evaluating maraviroc for HIV/AIDS has enrolled more than 2000 patients representing more than 750 patient years of follow up observation that began in December 2004. The studies have been fully recruited and are closed to further enrollment.
 
Based on their April 2006 meeting the DSMB recommended that the four Phase 2b/3 clinical studies for the investigational drug continue as currently designed. The DSMB further reported that they continue to see no evidence of maraviroc associated hepatotoxicity, including those patients receiving concomitant tipranavir. Their review of HIV-associated malignancies such as Non-Hodgkin's Lymphoma and Kaposi's Sarcoma, observed within the maraviroc Phase 2b/3 development program, found the incidence to be consistent with known rates of these malignancies in similar HIV-infected populations.
 
For more information about maraviroc clinical trials, please visit www.clinicaltrials.gov.
 
 
 
 
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