Relative Bioavailability Study of a Modified-Release Formulation of PF-06865571 in Healthy Adult Participants

PHASE1CompletedINTERVENTIONAL
Enrollment

12

Participants

Timeline

Start Date

August 13, 2019

Primary Completion Date

October 31, 2019

Study Completion Date

October 31, 2019

Conditions
Healthy Participants
Interventions
DRUG

PF-06865571 400 mg Immediate Release (IR) in Fed State

400 mg IR dose in fed state

DRUG

PF-06865571 50 mg Modified Release (MR) in Fed State

50 mg MR in fed state

DRUG

PF-06865571 400 mg MR in Fed State

400 mg MR in fed state

DRUG

PF-06865571 400 mg MR in Fasted State

400 mg MR in fasted state

Trial Locations (1)

B-1070

Brussels Clinical Research Unit, Brussels

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY

NCT04044053 - Relative Bioavailability Study of a Modified-Release Formulation of PF-06865571 in Healthy Adult Participants | Biotech Hunter | Biotech Hunter