Model‐informed drug development of voxelotor in sickle cell disease: Population pharmacokinetics in whole blood and plasma

Abstract Oxbryta (voxelotor) is a small‐molecule inhibitor of sickle hemoglobin (Hb) polymerization approved for patients with sickle cell disease (SCD) aged greater than or equal to 12 years at a dose of 1500 mg once daily (q.d.). Voxelotor binds preferentially to Hb, and voxelotor partitioning int...

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Bibliographic Details
Main Authors: Radojka M. Savic, Michelle L. Green, Karin Jorga, Michael Zager, Carla B. Washington
Format: Article
Language:English
Published: Wiley 2022-06-01
Series:CPT: Pharmacometrics & Systems Pharmacology
Online Access:https://doi.org/10.1002/psp4.12731