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Monogenic alpha thalassemia spectrum

MONDO:0100565

An instance of alpha thalessemia spectrum that is caused by an inherited monogenomic modification in an individual.

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

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Sub-types

HBA1-related alpha thalassemia spectrum (0) HBA2-related alpha thalassemia spectrum (0)

Broader categories

Disease (618) Hereditary disease (172) Hematologic disorder (160) Thalassemia (40) Inherited hemoglobinopathy (33) Hemoglobinopathy (30) Human disease (14) Alpha thalassemia spectrum (10) Erythrocyte disorder (6) Disease of genetic or genomic mechanism (2)

Trials to join now! 21 Not yet recruiting 3 Not yet finished but already full! 5 Completed 16 Terminated 1

Can extra care after transplant help older patients live better?

Disease control Terminated

This study tested two extra care programs—supportive palliative care and clinical management of other health issues—for older or frail patients who had a donor stem cell transplant. The goal was to see if these programs could improve quality of life and survival compared to stand…

Phase: PHASE2, PHASE3 • Sponsor: Fred Hutchinson Cancer Center • Aim: Disease control

Last updated Jun 27, 2026 08:10 UTC