Improving endpoints for sickle cell disease clinical trials: retaining consistency and clinical benefit

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Authors: Slimane Allali, Martina Bevacqua, Mariane de Montalembert
Cited by: 0
References: 15

Abstract

1. Sickle cell disease (SCD) is a common hemoglobin disorder characterized by chronic hemolytic anemia and severe acute vaso-occlusive events leading to multiple organ damage. It is responsible for...

Fields of Study & Subjects

Hemoglobinopathies and Related Disorders Statistical Methods in Clinical Trials Hemophilia Treatment and Research

Publication details

Journal / source
Expert Review of Hematology
Volume
19
Issue
4
Pages
357–359
Publication date
17 February 2026
Language
EN