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A Study to Evaluate Impact of Efanesoctocog Alfa on Long-term Joint Health in Participants With Hemophilia A

Active, not recruiting · NCT05911763

Conditions: Hemophilia A

At a glance

Research payments reported, 2025
$201,594
U.S. investigators named
27
Sites paid
26
Planned or actual enrollment
200

About the trial

Sponsor
Sanofi
Tested
Efanesoctocog Alfa BIVV001 (drug)
Dates
Started 2023-06-30; completion 2030-09-17
Results posted
Not yet

This is a prospective, observational, multi-center longitudinal cohort study to describe the real-world effectiveness, safety and treatment usage of efanesoctocog alfa in patients with hemophilia A treated per standard of care in the US and Japan. Patients will be enrolled in the study after the introduction of efanesoctocog alfa in the hemophilia treatment landscape in each study country. Decision to initiate treatment with commercially available efanesoctocog alfa will be made by the treating physician independently from the decision to include patients in the study. No study medication is provided. The data related to efanesoctocog alfa effectiveness, safety and usage will be collected…

From ClinicalTrials.gov, last updated 2026-09-29. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Sanofi US Services Inc. reported $201,594 in research payments for this study in 2025 (61 payments).

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.