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A Safety and Tolerability Study of CP-690,550 in Subjects With Hepatic Impairment and Normal Hepatic Function

Pfizer logo

Pfizer

Status and phase

Completed
Phase 1

Conditions

Hepatic Insufficiency

Treatments

Drug: CP-690,550

Study type

Interventional

Funder types

Industry

Identifiers

NCT00969813
A3921015

Details and patient eligibility

About

This study is designed to evaluate how CP-690,550 is handled by the body in healthy volunteers who have mild and moderate hepatic impairment compared to healthy volunteers with normal hepatic function. This study will also evaluate the safety and tolerability of CP-690,550.

Enrollment

18 patients

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy volunteers who have normal liver function, and subjects who have either mild or moderate liver impairment.

Exclusion criteria

  • Subjects with severe liver impairment
  • Subjects who have weakened immune systems

Trial design

18 participants in 3 patient groups

Normal hepatic function
Experimental group
Treatment:
Drug: CP-690,550
Drug: CP-690,550
Drug: CP-690,550
Mild hepatic impairment
Experimental group
Treatment:
Drug: CP-690,550
Drug: CP-690,550
Drug: CP-690,550
Moderate hepatic impairment
Experimental group
Treatment:
Drug: CP-690,550
Drug: CP-690,550
Drug: CP-690,550

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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