2-part Study to Assess Safety, Pharmacokinetics & Pharmacodynamics of CC-220 & Effect of Food on CC-220 in Healthy Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

65

Participants

Timeline

Start Date

November 1, 2012

Primary Completion Date

October 9, 2013

Study Completion Date

October 9, 2013

Conditions
Healthy
Interventions
DRUG

CC-220 0.03 mg

A single dose of CC-220 0.03 mg will be administered orally once a day.

DRUG

CC-220 0.1 mg

A single dose of CC-220 0.1 mg will be administered orally once a day.

DRUG

CC-220 0.3 mg

A single dose of CC-220 0.3 mg will be administered orally once a day.

DRUG

CC-220 1 mg

A single dose of CC-220 1 mg will be administered orally once a day.

DRUG

CC-220 2 mg

A single dose of CC-220 2 mg will be administered orally once a day.

DRUG

Placebo

A single dose of placebo will be administered orally once a day.

DRUG

CC-220

CC-220 4 mg will be administered orally once a day

DRUG

CC-220

CC-220 6 mg will be administered orally once a day

DRUG

CC-220

CC-220 1 mg will be administered orally once a day in each of 2 study periods - once with food and once without food

Trial Locations (1)

53704

Covance Clinical Research Unit, Madison

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Celgene

INDUSTRY

NCT01733875 - 2-part Study to Assess Safety, Pharmacokinetics & Pharmacodynamics of CC-220 & Effect of Food on CC-220 in Healthy Subjects | Biotech Hunter | Biotech Hunter