Single Dose Study to Assess the Safety, Tolerability and Pharmacokinetics(PK) of PF-06865571

PHASE1CompletedINTERVENTIONAL
Enrollment

17

Participants

Timeline

Start Date

March 16, 2017

Primary Completion Date

July 13, 2017

Study Completion Date

July 17, 2017

Conditions
Healthy
Interventions
DRUG

PF-06865571

Single ascending dose of PF-06865571 as extemporaneously prepared solution/suspension, once every 2 week in a cross over study: 5 mg, 50 mg, 500 mg, TBD (to be determined)/2000 mg.

DRUG

PF-06865571

Single ascending dose of PF-06865571 as extemporaneously prepared solution/suspension, once every 2 week in a cross over study: 15 mg, 150 mg, 1000 mg, TBD/2000 mg.

DRUG

PF-06865571

Single repeated (TBD mg) dose as extemporaneously prepared solution/suspension of PF-06865571.

DRUG

Placebo

Matching Placebo for PF-06865571 for each cohort.

Trial Locations (1)

06511

Pfizer New Haven Clinical Research Unit, New Haven

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY

NCT03092232 - Single Dose Study to Assess the Safety, Tolerability and Pharmacokinetics(PK) of PF-06865571 | Biotech Hunter | Biotech Hunter