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Enrolling by invitationPhase 2/3

Long-term Follow-up of Adult Men Treated for Hemophilia B With Gene Therapy

Follows adult men with hemophilia B who previously received etranacogene dezaparvovec gene therapy.

Plain-language title generated from the registry record
Registry title: Long-term Follow-up Study of Male Adults With Hemophilia B Previously Treated With Etranacogene Dezaparvovec (CSL222)

Key facts

Where
Berlin, GermanySee the site
Phase
Phase 2/3

Where in Germany

  • Vivantes Netzwerk fuer Gesundheit GmbHBerlin, GermanyNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
CSL Behring
Trial code
NCT05962398EU 2023-503765-37-00
Record updated
18 July 2025
Original description
The primary purpose of this study is to assess the long-term safety and efficacy in male adults with hemophilia B who were treated with CSL222 (CSL222) in parent studies CSL222_2001 (NCT03489291) or CSL222_3001 (NCT03569891).Read full original descriptionShow less

An Extension Study Assessing the Long-term Safety and Efficacy of Etranacogene Dezaparvovec (CSL222) Previously Administered to Adult Male Subjects With Hemophilia B

The primary purpose of this study is to assess the long-term safety and efficacy in male adults with hemophilia B who were treated with CSL222 (CSL222) in parent studies CSL222_2001 (NCT03489291) or CSL222_3001 (NCT03569891).

Inclusion: Received treatment with CSL222 in Study CSL222_2001 or Study CSL222_3001, and completed participation in Study CSL222_2001 or Study CSL222_3001 or at least 5 years have passed since receiving CSL222.

Exclusion: Not Applicable.

ClinicalTrials.gov NCT05962398 · EU CTIS 2023-503765-37-00