A molecular jewel for hemophilia A treatment

Julie Rayes, Sébastien Lacroix-Desmazes

Research output: Contribution to journalReview articlepeer-review

Abstract

In this issue of Blood, Seth Chhabra et al describe the engineering of a new therapeutic chimera composed of B domain-deleted (BDD) factor VIII (FVIII), FVIII-binding domain of von Willebrand factor (VWF), Fcg1 fragment, and XTEN polypeptides.1 The molecule, referred to as rFVIIIFc-VWF-XTEN or BIVV001, has a prolonged half-life that is independent from endogenous VWF and is hemostatically competent.

Original languageEnglish
Pages (from-to)1417-1419
Number of pages3
JournalBlood
Volume135
Issue number17
DOIs
Publication statusPublished - 23 Apr 2020

Bibliographical note

Funding Information:
Conflict-of-interest disclosure: J.R. declares no competing financial interests. S.L.-D. is the recipient of a research grant from Sanofi Genzyme and Sobi. n

Publisher Copyright:
© 2020 by The American Society of Hematology.

Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.

ASJC Scopus subject areas

  • Biochemistry
  • Immunology
  • Hematology
  • Cell Biology

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