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Clinical Trial Summary

The primary objective of this study is to obtain prospective baseline documentation of annualized bleeding rates (ABRs) and treatment under standard-of-care (SOC) therapy among participants with hemophilia A or B. Participants in the study may be eligible to enroll in future planned interventional studies to be conducted by Sponsor.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05605678
Study type Observational
Source ApcinteX Ltd
Contact Centessa Pharmaceuticals
Phone 617 468 5770
Email presentprogram@centessa.com
Status Recruiting
Phase
Start date December 9, 2022
Completion date November 2024

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