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Data Registry in Chinese Hemophilia A and B Patients

I

Institute of Hematology & Blood Diseases Hospital, China

Status

Completed

Conditions

Hemophilia B
Hemophilia A

Study type

Observational

Funder types

Other

Identifiers

NCT07101224
QT2016004

Details and patient eligibility

About

This is an open-label, prospective, multi-center, patient registry in Chinese Hemophilia A and B patients treated with anti-hemophilic coagulation factor replacement therapy.

Enrollment

200 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

Subjects must meet all of the following inclusion criteria to be eligible for enrollment into the study:

  1. Hemophilia A and Hemophilia B patient diagnosed;
  2. Taking anti-hemophilic coagulation factor replacement therapy during the 2 year registry period.

Exclusion Criteria:

  1. Unwilling or unable to follow the terms of the protocol.

Trial design

200 participants in 2 patient groups

Hemophilia A
Hemophilia B

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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