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