Study of Controlled Release Formulations of CE-224,535 Against the Immediate Release Formulation in Normal Volunteers

PHASE1CompletedINTERVENTIONAL
Enrollment

16

Participants

Timeline

Start Date

July 31, 2008

Primary Completion Date

August 31, 2008

Study Completion Date

August 31, 2008

Conditions
Rheumatoid Arthritis
Interventions
DRUG

suspension IR

50 mg IR suspension once daily for one day

DRUG

CR 1

50 mg shorter release CR once daily for one day

DRUG

CR 2

50 mg medium release CR once daily for one day

DRUG

CR 3

longer release SR formulation once daily for one day

Trial Locations (1)

06511

Pfizer Investigational Site, New Haven

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY