Prevalence of Inhibitor Development in Hemophilia A Patients Receiving Coageight: A Multicenter Cross-sectional Observational Study

NCT07791836 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 262

Last updated 2026-08-28

No results posted yet for this study

Summary

This is a cross-sectional, observational, multi-center study to assess the prevalence of inhibitor development in hemophilia A patients receiving Coageight (rFVIII-Fc, AryoGen Pharmed Co.).

Conditions

Interventions

DRUG

efmoroctocog alfa

This study assesses patients with a history of at least 10 exposure days (EDs) to recombinant factor VIII with Fc fusion (Coageight) within the 12 months prior to enrollment.

Sponsors & Collaborators

  • AryoGen Pharmed Co.

    lead INDUSTRY

Eligibility

Min Age
2 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-08-23
Primary Completion
2027-02-20
Completion
2027-02-20

Countries

  • Iran

Study Locations

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Entities

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 NCT07791836 on ClinicalTrials.gov