A Dose Ranging Study Of PF-00868554 In Combination With PEGASYS And COPEGUS In Patients With Chronic Hepatitis C Genotype 1 Infection

PHASE2CompletedINTERVENTIONAL
Enrollment

35

Participants

Timeline

Start Date

August 31, 2008

Primary Completion Date

March 31, 2010

Study Completion Date

March 31, 2010

Conditions
Hepatitis C
Interventions
DRUG

PF-00868554

500 mg BID administered as 5x100 mg tablets for 4 weeks in combination with standard of care; standard of care continued for an additional 44 weeks.

DRUG

PF-00868554

300 mg BID administered as 3x100 mg tablets for 4 weeks in combination with standard of care; standard of care continued for an additional 44 weeks

DRUG

PF-00868554

200 mg BID administered as 2x100 mg tablets for 4 weeks in combination with standard of care; standard of care continued for an additional 44 weeks

DRUG

Placebo

Placebo administered for 4 weeks in combination with standard of care; standard of care continued for an additional 44 weeks

Trial Locations (10)

10021

Pfizer Investigational Site, New York

10065

Pfizer Investigational Site, New York

32803

Pfizer Investigational Site, Orlando

37205

Pfizer Investigational Site, Nashville

74135

Pfizer Investigational Site, Tulsa

78215

Pfizer Investigational Site, San Antonio

92037

Pfizer Investigational Site, La Jolla

94115

Pfizer Investigational Site, San Francisco

01107

Pfizer Investigational Site, Springfield

00909

Pfizer Investigational Site, Santurce

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY

NCT00720434 - A Dose Ranging Study Of PF-00868554 In Combination With PEGASYS And COPEGUS In Patients With Chronic Hepatitis C Genotype 1 Infection | Biotech Hunter | Biotech Hunter