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

Primary Purpose

Hemophilia A With Inhibitor

Status
Unknown status
Phase
Locations
Japan
Study Type
Observational
Intervention
Sponsored by
Nara Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an observational trial for Hemophilia A With Inhibitor focused on measuring hemophilia A, inhibitor, bypassing therapy, factor VIII

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)MaleDoes not accept 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

Sites / Locations

  • Department of Pediatrics

Arms of the Study

Arm 1

Arm Type

Arm Label

Combination therapy

Arm Description

Effects of aPCC reaction in the presence of FVIII

Outcomes

Primary Outcome Measures

Evaluation of coagulation effects using patients' plasmas by FXa/thrombin/plasmin generation tests and clot waveform analysis
Evaluation of coagulation effects using patients' whole bloods by ROTEM and T-TAS

Secondary Outcome Measures

Full Information

First Posted
September 15, 2015
Last Updated
September 17, 2015
Sponsor
Nara Medical University
Collaborators
Shire
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1. Study Identification

Unique Protocol Identification Number
NCT02554526
Brief Title
Basic Study of Combination Therapy Based on APCC-induced FVllI Activation in Hemophilia A Patients With Inhibitors
Official Title
Basic Study on Novel Therapeutic Strategy With Bypassing Agent Therapy in Hemophilia A Patients With Inhibitors
Study Type
Observational

2. Study Status

Record Verification Date
September 2015
Overall Recruitment Status
Unknown status
Study Start Date
September 2015 (undefined)
Primary Completion Date
March 2017 (Anticipated)
Study Completion Date
December 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Nara Medical University
Collaborators
Shire

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemophilia A With Inhibitor
Keywords
hemophilia A, inhibitor, bypassing therapy, factor VIII

7. Study Design

Enrollment
10 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Combination therapy
Arm Description
Effects of aPCC reaction in the presence of FVIII
Primary Outcome Measure Information:
Title
Evaluation of coagulation effects using patients' plasmas by FXa/thrombin/plasmin generation tests and clot waveform analysis
Time Frame
up to 10 months
Title
Evaluation of coagulation effects using patients' whole bloods by ROTEM and T-TAS
Time Frame
up to 15 months

10. Eligibility

Sex
Male
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Study Population Description
We guess that there are approximately 200-300 hemophilia A patients with inhibitors in our country. We have approximately 20 out-patients in our hospital. Based on this information, we set up the patients subjects (n=10).
Sampling Method
Non-Probability Sample
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Keiji Nogami, MD, PhD
Phone
+81-744-29-8881
Email
roc-noga@naramed-u.ac.jp
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Midori Shima, MD, PhD
Organizational Affiliation
Nara Medical University
Official's Role
Study Director
Facility Information:
Facility Name
Department of Pediatrics
City
Kashihara
State/Province
Nara
ZIP/Postal Code
634-8522
Country
Japan
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Keiji Nogami, MD, PhD
Phone
+81-744-29-8881
Email
roc-noga@naramed-u.ac.jp
First Name & Middle Initial & Last Name & Degree
Tomoko Matsumoto, PhD

12. IPD Sharing Statement

Learn more about this trial

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

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