Evaluation of SCT800 in Prophylaxis Therapy on Previous Treated Patients With Severe Hemophilia A

PHASE3CompletedINTERVENTIONAL
Enrollment

73

Participants

Timeline

Start Date

January 21, 2019

Primary Completion Date

January 16, 2020

Study Completion Date

January 16, 2020

Conditions
Hemophilia A
Interventions
DRUG

Recombinant Human Coagulation FVIII

Participant received SCT800 for prophylaxis with 25 - 50 IU/kg injection once every other day or three times per week for 6 months.

Trial Locations (1)

Unknown

Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin

Sponsors

Collaborators (2)

All Listed Sponsors
collaborator

Chinese Academy of Medical Sciences

OTHER

collaborator

Parexel

INDUSTRY

collaborator

Q2 Solutions

INDUSTRY

lead

Sinocelltech Ltd.

INDUSTRY