StevenWPipeMD
Pediatric Hematology & Oncology • Ann Arbor, MIPediatric Coagulation Disorder Hematology, Pediatric Platelet Disorder Hematology
Professor, Pediatrics & Communicable Diseases, University of Michigan Medical School
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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
- 27 citationsBiological mechanisms underlying inter-individual variation in factor VIII clearance in haemophilia.Peter Turecek, Jill M. Johnsen, Steven W. Pipe, James S. O’Donnell
Haemophilia. 2020-06-28 - 23 citationsProgress in the molecular biology of inherited bleeding disorders.Steven W. Pipe, Katherine A. High, Kazuo Ohashi, A. U. Ural, David Lillicrap
Haemophilia. 2008-07-01 - 117 citationsValoctocogene Roxaparvovec Gene Therapy for Hemophilia A.Margareth C Ozelo, Johnny Mahlangu, K John Pasi, Adam Giermasz, Andrew D Leavitt
The New England Journal of Medicine. 2022-03-17
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
- 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
- Hemgenix Gene Therapy Benefits Sustained for 2 Years in Phase 3 TrialDecember 14th, 2022
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