Study of Recombinant Human Coagulation Factor VIIa for Injection (FⅦa) in Patients With Hemophilia.

PHASE1UnknownINTERVENTIONAL
Enrollment

24

Participants

Timeline

Start Date

December 1, 2020

Primary Completion Date

December 1, 2021

Study Completion Date

December 1, 2021

Conditions
Hemophilia A With InhibitorHemophilia B With Inhibitor
Interventions
DRUG

TQG203

TQG203,30µg/kg body weight, will be administered as intravenous (i.v.) administration over a period about 2minutes (min) on Study Day 1 once.

DRUG

TQG203/NovoSeven®

In each of the two study periods (separated by a washout about two days),a single dose of TQG203 or NovoSeven® will be administered.TQG203 or NovoSeven®,90µg/kg body weight, will be administered as intravenous (i.v.) administration over a period about 2minutes (min) on Study Day 1.

DRUG

TQG203

TQG203,180µg/kg body weight, will be administered as intravenous (i.v.) administration over a period about 2minutes (min) on Study Day 1 once.

Trial Locations (1)

300020

RECRUITING

Hematology Hospital of Chinese Academy of Medical Sciences, Tianjin

All Listed Sponsors
lead

Chia Tai Tianqing Pharmaceutical Group Co., Ltd.

INDUSTRY