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HBA1-related alpha thalassemia spectrum

MONDO:0100561

Mild microcytic anemia caused by biallelic variation in the HBA1 gene.

Also known as: alpha-thalassemia trait

14 clinical trials for this condition and its sub-types.

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Broader categories

Disease (680) Hereditary disease (176) Hematologic disorder (170) Thalassemia (47) Inherited hemoglobinopathy (35) Hemoglobinopathy (31) Human disease (14) Alpha thalassemia spectrum (10) Erythrocyte disorder (6) Disease of genetic or genomic mechanism (2)

Trials to join now! 6 Not yet recruiting 1 Not yet finished but already full! 2 Completed 5

New hope for kids: drug may prevent transplant complications

Disease control Not yet recruiting

This study tests whether adding the drug vorinostat to standard care can prevent graft-versus-host disease (GVHD) in children and young adults (ages 1-26) with non-cancerous blood disorders who are getting a bone marrow transplant. GVHD is a serious complication where donor cells…

Phase: PHASE2 • Sponsor: Sung Won Choi • Aim: Disease control

Last updated Jul 02, 2026 00:00 UTC