Status:

COMPLETED

An Open Label Study To Evaluate The Safety and Kinetics of Nelfinavir in Subjects With HIV and Hepatitis C

Lead Sponsor:

Pfizer

Conditions:

HIV Infection

Hepatitis C

Eligibility:

All Genders

18-60 years

Phase:

PHASE4

Brief Summary

The purpose of this study is to confirm the safety, efficacy and delineate the pharmacokinetic properties of nelfinavir in HIV/ Hepatitis C coinfected subjects with Child Pugh A compensated cirrhosis ...

Eligibility Criteria

Inclusion

  • HIV/ Hepatitic C co infected with documented HCV viremia evidence for cirrhosis and or hepatic fibrosis on liver biopsy, positive fibrosis index, stable health

Exclusion

  • Decompensated cirrhosis (Child Pugh B or C)
  • Pregnant or lactating women
  • History of previous antiretrovirals \> 14 days

Key Trial Info

Start Date :

October 1 2005

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 1 2006

Estimated Enrollment :

12 Patients enrolled

Trial Details

Trial ID

NCT00141284

Start Date

October 1 2005

End Date

December 1 2006

Last Update

May 16 2011

Active Locations (5)

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Page 1 of 2 (5 locations)

1

Pfizer Investigational Site

Bakersfield, California, United States, 93301

2

Pfizer Investigational Site

Miami, Florida, United States, 33136

3

Pfizer Investigational Site

Shreveport, Louisiana, United States, 71130

4

Pfizer Investigational Site

Dallas, Texas, United States, 75390

An Open Label Study To Evaluate The Safety and Kinetics of Nelfinavir in Subjects With HIV and Hepatitis C | DecenTrialz