Basic Study of Combination Therapy Based on APCC-induced FVllI Activation in Hemophilia A Patients With Inhibitors

Nara Medical University

Status: Unknown

Conditions: Hemophilia A With Inhibitor

Study type: Observational

Funder types: Other; Industry

Identifiers

NCT02554526

J150100036

Details and patient eligibility

About

Using whole blood samples and plasma samples obtained from some hemophilia A patients with inhibitors, the investigators will perform the coagulation assessment in the co-presence of aPCC and factor VIII by comprehensive coagulation assays and flow chamber analysis under blood flow conditions.

Full description

Comprehensive coagulation assays using recently popular rotational thromboelastometry (ROTEM), factor Xa/thrombin/plasmin generation test, and coagulation wave analysis and recently developed flow chamber system under blood flow conditions (T-TAS®) will be used. A bypassing agent, aPCC (Feiba®) and recombinant factor VIII (Advate®) will be added ex vivo to whole blood and plasma samples from patients with hemophilia A with inhibitors to compare with the coagulation effects of aPCC in the presence of factor VIII and those of aPCC in its absence under the conditions close to the physiological condition. Furthermore, the difference in the coagulation effects by the difference in inhibitor epitopes will be examined.

Enrollment: 10 estimated patients

Sex: Male

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients with hemophilia A with inhibitors (Inhibitor titer; >0.5 Bethesda U/ml)
• Patients with agreement consents with the patients signatures

Exclusion criteria

• Patients that do not fill the conditions described above

Trial design

10 participants in 1 patient group

Combination therapy

Description:

Effects of aPCC reaction in the presence of FVIII