Phase 1/2 Study to Evaluate the Safety, Tolerability and Pharmacokinetics of HQK-1001 Administered Daily in Patients With Sickle Cell Disease

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

24

Participants

Timeline

Start Date

March 31, 2009

Primary Completion Date

July 31, 2010

Conditions
Sickle Cell Disease
Interventions
DRUG

Placebo

Matching placebo capsule. Administered orally once a day on dosing days.

DRUG

HQK-1001

HQK-1001 capsules. 10 mg/kg, 20 mg/kg or 30 mg/kg administered once a day on dosing days.

Trial Locations (9)

7

University of the West Indies, Mona, Kingston

21205

Johns Hopkins School of Medicine, Baltimore

27599

UNC Comprehensive Sickle Cell Program, Chapel Hill

30912

Medical College of Georgia, Augusta

32117

Century Clinical Research, Inc., Daytona Beach

35758

Trialogic Research, Madison

60612

University of Illinois at Chicago, Chicago

77030

Texas Children's Cancer Center and Hematology Service, Houston

94609

Children's Hospital and Research Center at Oakland, Oakland

Sponsors
All Listed Sponsors
lead

HemaQuest Pharmaceuticals Inc.

INDUSTRY