A Study To Evaluate The Effect Of Itraconazole On Pharmacokinetics Of PF-06463922 In Healthy Volunteers

PHASE1CompletedINTERVENTIONAL
Enrollment

16

Participants

Timeline

Start Date

August 16, 2016

Primary Completion Date

March 31, 2017

Study Completion Date

May 3, 2017

Conditions
Healthy
Interventions
DRUG

PF-06463922

Single oral dose of PF-06463922 50 mg on Day 1 of Period 1 and Day 5 of Period 2

DRUG

PF-06463922

Single oral dose of PF-06463922 75 mg on Day 1 of Period 1 and Day 5 of Period 2

DRUG

PF-06463922

Single oral dose of PF-06463922 100 mg on Day 1 of Period 1 and Day 5 of Period 2

DRUG

PF-06463922

Highest safe single oral dose (mg) of PF-06463922 identified in the previous cohorts will be administered on Day 1 of Period 1 and Day 5 of Period 2

DRUG

Itraconazole

200 mg oral dose of itraconazole on Days 1 to 11 during Period 2

Trial Locations (1)

B-1070

Pfizer Clinical Research Unit, Brussels

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY

NCT02838264 - A Study To Evaluate The Effect Of Itraconazole On Pharmacokinetics Of PF-06463922 In Healthy Volunteers | Biotech Hunter | Biotech Hunter