Merimepodib (MMPD) in Triple Combination for the Treatment of Chronic Hepatitis C
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|ClinicalTrials.gov Identifier: NCT00088504|
Recruitment Status : Completed
First Posted : July 28, 2004
Last Update Posted : December 21, 2007
This trial is designed to test whether or not the addition of merimepodib (MMPD) to the standard therapy of pegylated interferon and ribavirin will result in a positive treatment response for people who have not previously responded to this therapy. Approximately 315 subjects will be enrolled in this research study at approximately 55 clinical sites in the United States. There will be three study groups. Everyone in the study will receive Pegasys® (pegylated interferon) and Copegus® (ribavirin) at the normally prescribed doses. Two of the groups will also receive the study drug merimepodib (MMPD) twice a day, one group at each dose level being tested. The third group will take a placebo instead of MMPD, with the Pegasys® and Copegus®.
After the first 24 weeks of treatment, blood tests will be done to see if subjects are responding to treatment. If they are responding, they will continue receiving study treatment in the study for another 24 weeks. If they are not responding, they will stop study treatment. Everyone who is responding will be monitored for 24 weeks after the last dose of medication, to see how long the response lasts.
Evaluations will be performed during the study to look at the safety of the Pegasys®/Copegus® and MMPD or placebo combination, and to see how the combination is working by measuring Hepatitis C Virus in the blood.
At some of the clinical sites performing the study, some subjects may also participate in additional testing to look at the metabolism of the drugs, or to look at the immune response to Hepatitis C virus infection and treatment.
|Condition or disease||Intervention/treatment||Phase|
|Hepatitis C Hepatitis||Drug: Merimepodib Drug: PEG-Interferon-alpha 2a (Pegasys®) Drug: Ribavirin (Copegus®)||Phase 2|
|Study Type :||Interventional (Clinical Trial)|
|Enrollment :||315 participants|
|Intervention Model:||Parallel Assignment|
|Official Title:||A Phase 2b Study of Merimepodib in Combination With Pegylated Interferon Alfa-2a (Pegasys®) and Ribavirin in Subjects With Chronic Hepatitis C Non-Responsive to Prior Therapy With Pegylated Interferon Alfa and Ribavirin|
|Study Start Date :||July 2004|
|Actual Study Completion Date :||October 2006|
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00088504
|Study Director:||Robert Kauffman, MD, PhD||Vertex Pharmaceuticals Incorporated|