Peg-Intron/Ribavirin in G 1 HCV for Non-Extended Versus 24 Week Extended Treatment After 24 Weeks (Study P04144)(COMPLETED)

PHASE4CompletedINTERVENTIONAL
Enrollment

160

Participants

Timeline

Start Date

March 31, 2005

Primary Completion Date

July 31, 2008

Study Completion Date

July 31, 2008

Conditions
Hepatitis C, Chronic
Interventions
BIOLOGICAL

PegIntron (peginterferon alfa-2b; SCH 54031)

Powder for injection in vial (120 microgram strength), subcutaneous, dose of 1.5 micrograms/kg weekly for 24 weeks during the pilot treatment program

BIOLOGICAL

PegIntron (peginterferon alfa-2b; SCH 54031)

Powder for injection in vial (120 microgram strength), subcutaneous, dose of 1.5 micrograms/kg weekly for 24 weeks during the pilot treatment program followed by 1.2 to 1.5 microgram/kg weekly for 24 weeks during the extended treatment program

DRUG

Ribavirin

200 mg capsules, oral, weight-based dose of 1000 or 1200 mg, daily for for 24 weeks during the pilot treatment program

DRUG

Ribavirin

200 mg capsules, oral, weight-based dose of 1000 or 1200 mg, daily for for 24 weeks during the pilot treatment program and for 24 weeks during the extended treatment program

All Listed Sponsors
lead

Merck Sharp & Dohme LLC

INDUSTRY

NCT00202839 - Peg-Intron/Ribavirin in G 1 HCV for Non-Extended Versus 24 Week Extended Treatment After 24 Weeks (Study P04144)(COMPLETED) | Biotech Hunter | Biotech Hunter