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Multiple Oral Doses Of PH-797804 In Healthy Japanese Adult Subjects

Pfizer logo

Pfizer

Status and phase

Completed
Phase 1

Conditions

Healthy

Treatments

Drug: 10 mg
Drug: 5 mg
Drug: 1 mg

Study type

Interventional

Funder types

Industry

Identifiers

NCT01217918
A6631027

Details and patient eligibility

About

Study A6631027 will evaluate the safety, tolerability and pharmacokinetics of PH-797804 when administered to healthy Japanese subjects once a day (QD) for 10 days.

Enrollment

30 patients

Sex

All

Ages

18 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy Volunteers
  • Japanese

Exclusion criteria

  • Subjects with clinically significant skin lesions
  • Subjects with known tuberculosis infection

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

30 participants in 3 patient groups

Cohort 1
Experimental group
Description:
PH-797804
Treatment:
Drug: 1 mg
Cohort 2
Experimental group
Description:
PH-797804
Treatment:
Drug: 5 mg
Cohotr 3
Experimental group
Description:
PH-797804
Treatment:
Drug: 10 mg

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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