Clinical Trial In Healthy Volunteers And Health Elderly Volunteers To Evaluate The Safety, Tolerability And Blood Concentration After Single And Multiple Escalating Oral Doses Of PF-06751979.

PHASE1CompletedINTERVENTIONAL
Enrollment

46

Participants

Timeline

Start Date

June 13, 2016

Primary Completion Date

January 5, 2017

Study Completion Date

January 5, 2017

Conditions
Healthy Subjects
Interventions
DRUG

PF-06751979 single dose

PF-06751979 administered as a single dose suspension in cross-over fashion. Each subject may receive up to 4 study treatments (placebo and up to 3 doses of PF 06751979). The planned dose levels are 200 mg, 400 mg, 700 mg, 200 mg fed (these doses are subject to change based on emerging data).

DRUG

Placebo single dose

Matched Placebo suspension administered as single dose

DRUG

PF-06751979 multiple ascending dose

PF-06751979 suspension administered daily for 14 consecutive days to parallel cohorts. The planned dose levels are mg, 100 mg, 200 mg, 340 mg (these are subject to change based on emerging data).

DRUG

Placebo multiple ascending dose

Matched placebo suspension administered daily for 14 consecutive days.

DRUG

PF-06751979 multiple dose

PF-06751979 suspension administered daily for 14 consecutive days. The planned dose level is 340 mg (this is subject to change based on emerging data).

DRUG

Placebo multiple elderly dose

Multiple dose administration to Healthy Elderly Subjects (Placebo)

Trial Locations (1)

B-1070

Pfizer Clinical Research Unit, Brussels

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY

NCT02793232 - Clinical Trial In Healthy Volunteers And Health Elderly Volunteers To Evaluate The Safety, Tolerability And Blood Concentration After Single And Multiple Escalating Oral Doses Of PF-06751979. | Biotech Hunter | Biotech Hunter