Valopicitabine When Administered Alone and in Combination With Interferon to Treatment-Naive Patients With Hepatitis C

• Status: Completed
• Trial end date: 1969-12-31
• Target enrollment: 0
• Participant gender: All

Summary

This study is being conducted in treatment-naive patients (no previous hepatitis C treatment) to evaluate the safety of valopicitabine (NM283) alone and together with pegylated interferon, a drug approved by the Food and Drug Administration for the treatment of hepatitis C infection. This study is also evaluating the ability of valopicitabine to decrease the amount of hepatitis C virus in the body. The results for patients taking valopicitabine alone will be compared with the results for patients taking valopicitabine together with pegylated interferon.

• Phase: Phase 1/Phase 2

Details

• Lead Sponsor: Merck Sharp & Dohme Corp.
• Treatments: Interferons; Peginterferon alfa-2b

Criteria

Inclusion Criteria:

• Documented clinical history compatible with genotype-1, chronic hepatitis C infection

• Treatment-naive (patient has received no previous therapy for hepatitis C viral infection)

Other protocol-defined inclusion criteria may apply.

Exclusion Criteria:

• Patient is pregnant

• Patient is co-infected with hepatitis B or HIV

Other protocol-defined exclusion criteria may apply.