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Office
1500 E Medical Center Dr
D4207 MPB
Ann Arbor, MI 48109Phone+1 734-232-9335Fax+1 734-615-0464
Education & Training
- University of MichiganFellowship, Pediatric Hematology/Oncology, 1993 - 1996
- University of Toronto Faculty of MedicineClass of 1989
Certifications & Licensure
- MI State Medical License 1996 - 2025
- American Board of Pediatrics Pediatric Hematology-Oncology
Clinical Trials
- Dose Confirmation Trial of AAV5-hFIXco-Padua Start of enrollment: 2018 Jul 24
- HOPE-B: Trial of AMT-061 in Severe or Moderately Severe Hemophilia B Patients Start of enrollment: 2018 Jun 27
- Dose-finding Study of SPK-8016 Gene Therapy in Patients With Hemophilia A to Support Evaluation in Individuals With FVIII Inhibitors Start of enrollment: 2019 Jan 30
Roles: Contact
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Publications & Presentations
PubMed
- Operationalising a Haemophilia Gene Editing Lexicon for Practical Use.William McKeown, Cedric Hermans, Carmen Unzu, Mark A Kay, Flora Peyvandi
Haemophilia. 2025-01-27 - Accurate evaluation of factor VIII activity of efanesoctocog alfa in the presence of emicizumab.Christophe Nougier, Steven W Pipe, Ingrid Pabinger, Claire Pouplard, Roger E G Schutgens
Journal of Thrombosis and Haemostasis. 2025-01-09 - Extending health equity to people with moderate and mild hemophilia A: revisiting the HAVEN 6 trial.Cedric Hermans, Michiel Coppens, Giuliana Ventriglia, Gavin Ling, Michaela Lehle
Research and Practice in Thrombosis and Haemostasis. 2025-01-01
Abstracts/Posters
- One Year Data from a Phase 2b Trial of AMT-061 (AAV5-Padua hFIX variant), an Enhanced Vector for Gene Transfer in Adults with Severe or Moderate-Severe Hemophilia BSteven Pipe, 61st Annual American Society of Hematology Meeting, Orlando, FL, 12/8/2019
Lectures
- Moving Beyond Factor: Shifting the Paradigm in Hemophilia Through Gene Therapy61st Annual American Society of Hematology Meeting - Orlando, FL - 12/7/2019
- Fitusiran, an RNAi Therapeutic Targeting Antithrombin to Restore Hemostatic Balance in Patients with Hemophilia a or B with or without Inhibitors: Management of Acute ...61st Annual American Society of Hematology Meeting - Orlando, FL - 12/7/2019
- First-in-human Gene Therapy Study of AAVhu37 Capsid Vector Technology in Severe Hemophilia A61st Annual American Society of Hematology Meeting - Orlando, FL - 12/7/2019
Press Mentions
- CSL Reports Promising Four-Year Data on Gene Therapy for Hemophilia BFebruary 9th, 2025
- Gene Therapy Can Transform Life for People with Hemophilia. But Some Patients Don’t Want ItJanuary 29th, 2023
- Most Patients Bleed-Free at 3 Years After Roctavian in GENEr8-1 TrialJanuary 13th, 2023
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