EMISTAT: Impact of Emicizumab on Activated Clotting Time Using the i-STAT Alinity Analyzer

Sponsor
University Hospital, Grenoble (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05856903
Collaborator
(none)
15
20.1

Study Details

Study Description

Brief Summary

Emicizumab (Hemlibra®) is a subcutaneous hemostatic treatment approved in 2019 for the prophylaxis in severe hemophilia A. Emicizumab is a bispecific monoclonal antibody mimicking factor VIIIa that provides a constant level of coagulation similar to that observed in minor haemophilia A patients whose factor VIII level is 10-15%. Although the correction of plasma coagulation in vivo is only partial, emicizumab strongly shortens the in vitro coagulation times involving the intrinsic pathway such as aPTT(activated partial thromboplastin time).

The investigators will evaluate the effect of emicizumab on a coagulation test (Activating clotting time (ACT i-STAT Alinity)) used as a point of care device to monitor heparin therapies during cardiac surgeries (cardiopulmonary bypass) and cardiac catheterizations. Because ACT is activated through the intrinsic pathway, it may also be shortened by emicizumab. Prophylactic treatment with emicizumab would make it impossible to use ACT for heparin therapy in a hemophiliac patient benefiting from this treatment.

The aim of this in vitro study is to assess the effect of emicizumab on the in vitro heparin-induced ACT increase in severe hemophilia A patients treated with emicizumab and in healthy volunteers (measurement on the i- STAT Alinity) thanks to in vitro blood spiking experiments.

Some data have already been published with other ACT devices (Hemochron..) but never with the i-STAT Alinity device which uses a different technology and other reagents.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: ACT

Study Design

Study Type:
Observational
Anticipated Enrollment :
15 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Impact of Emicizumab on ACT (Activated Clotting Time) Using the i-STAT Alinity Analyzer: In Vitro Study in Severe Hemophiliacs A and Healthy Volunteers
Anticipated Study Start Date :
Jun 1, 2023
Anticipated Primary Completion Date :
Feb 1, 2025
Anticipated Study Completion Date :
Feb 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Severe hemophiliac patients under emicizumab

Diagnostic Test: ACT
ACT will be measured : after in vitro spiking with unfractionated heparin of blood samples from severe hemophilia A patients already treated with emicizumab after in vitro spiking with unfractionated heparin with or without emicizumab of blood samples from healthy volunteers

Healthy volunteers

Diagnostic Test: ACT
ACT will be measured : after in vitro spiking with unfractionated heparin of blood samples from severe hemophilia A patients already treated with emicizumab after in vitro spiking with unfractionated heparin with or without emicizumab of blood samples from healthy volunteers

Outcome Measures

Primary Outcome Measures

  1. Modification of ACT by emicizumab [Day 0]

    Modification of the in vitro heparin-induced ACT increase by emicizumab

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion criteria:
  • severe hemophiliacs under emicizumab ( > 4 weeks)
Exclusion Criteria:
  • infusion of factor VIII < 5 days

  • patients refusing to participate in the study

  • protected persons

  • anticoagulants

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University Hospital, Grenoble

Investigators

  • Principal Investigator: Raphaël MARLU, MD, Grenoble Alpes University Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
University Hospital, Grenoble
ClinicalTrials.gov Identifier:
NCT05856903
Other Study ID Numbers:
  • 38RC23.0124
  • 2023-A00897-38
First Posted:
May 12, 2023
Last Update Posted:
May 12, 2023
Last Verified:
May 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University Hospital, Grenoble
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 12, 2023