Register of Patients With haEmophilia A tReated With Afstyla®

NCT04675541 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 62

Last updated 2025-01-08

No results posted yet for this study

Summary

Record real life data of patients with Hemophilia A and treated with Afstyla® to assess the effectiveness and the safety of the treatment used as prophylaxis, prevention of bleeding (e.g. surgery) or on-demand treatment during 3 years after patient inclusion

Conditions

  • Haemophilia A

Interventions

BIOLOGICAL

Afstyla®

Solution for injection

Sponsors & Collaborators

  • CSL Behring

    lead INDUSTRY

Principal Investigators

  • Study Director · CSL Behring SA

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-09-24
Primary Completion
2024-12-31
Completion
2024-12-31

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04675541 on ClinicalTrials.gov