Evaluate Efficacy and Safety of Recombinant Factor VIII (rFVIII)Treatment of Severe or Moderately Severe Hemophilia A

PHASE3UnknownINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

August 31, 2016

Primary Completion Date

October 31, 2017

Study Completion Date

December 31, 2017

Conditions
Hemophilia A
Interventions
DRUG

Recombinant Factor VIII (50 IU/kg)

DRUG

Recombinant Factor VIII (On-demand treatment)

Trial Locations (4)

200025

NOT_YET_RECRUITING

Ruijin Hospital Shanghai Jiaotong University School of Medicine, Shanghai

230001

RECRUITING

Anhui provincial hospital, Hefei

300020

RECRUITING

Blood Diseases Hospital, Chinese Academy of Medical Science (Institute of Hematology), Tianjin

030001

NOT_YET_RECRUITING

Second hospital of Shanxi Medical University, Taiyuan

All Listed Sponsors
lead

Chia Tai Tianqing Pharmaceutical Group Co., Ltd.

INDUSTRY