Hemophilia Non-Interventional Study Prior to SerpinPC Intervention

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.

See also
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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

Hemophilia Non-Interventional Study Prior to SerpinPC Intervention (PRESent-5)

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms