Long-term Follow-up Study of Subjects with Hemophilia B Previously Treated with CSL222
Research type
Research Study
Full title
An Extension Study Assessing the Long-term Safety and Efficacy of Etranacogene Dezaparvovec (CSL222) Previously Administered to Adult Male Subjects with Hemophilia B
IRAS ID
1008420
Contact name
Rita Baptista
Contact email
Sponsor organisation
CSL Behring LLC
Clinicaltrials.gov Identifier
Research summary
The purpose of this study, CSL222_3003, is to gather information about how safe and how well
CSL222 works. You will be observed for up to 15 years after you were dosed.REC name
North East - York Research Ethics Committee
REC reference
23/NE/0196
Date of REC Opinion
24 Nov 2023
REC opinion
Further Information Favourable Opinion