An Assessment of Prasugrel on Healthy Adults and Sickle Cell Adults

PHASE1CompletedINTERVENTIONAL
Enrollment

26

Participants

Timeline

Start Date

July 31, 2010

Primary Completion Date

January 31, 2011

Study Completion Date

January 31, 2011

Conditions
Anemia, Sickle Cell
Interventions
DRUG

Prasugrel

Oral, daily for 12 days

Trial Locations (1)

SE 1 1YR

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., London

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Daiichi Sankyo Co., Ltd.

INDUSTRY

lead

Eli Lilly and Company

INDUSTRY