Hemolytic anemia
MONDO:0003664Anemia resulting from the premature destruction of the peripheral blood red cells. It may be congenital or it may be caused by infections, medications, or malignancies.
Also known as: anaemia hemolytic, anemia hemolytic, anemia, hemolytic, hemolytic anemia
188 clinical trials for this condition and its sub-types, 19 tagged with Hemolytic anemia itself.
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Sub-types of Hemolytic anemia
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Paroxysmal nocturnal hemoglobinuria 73 trials
2 sub-types
- Paroxysmal nocturnal hemoglobinuria 1 0 trials
- Paroxysmal nocturnal hemoglobinuria 2 0 trials
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Autoimmune hemolytic anemia 49 trials · 72 incl. sub-types
7 sub-types
- Autoimmune hemolytic anemia, warm type 29 trials
- Evans syndrome 19 trials
- Autoimmune hemolytic anemia, cold type 2 trials · 15 incl. sub-types Sub-types →
- Mixed-type autoimmune hemolytic anemia 1 trial
- Drug-induced autoimmune hemolytic anemia 0 trials
- Giant cell hepatitis with autoimmune hemolytic anemia 0 trials
- Neonatal autoimmune hemolytic anemia 0 trials
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Familial hemolytic anemia 4 trials · 27 incl. sub-types
23 sub-types
- Congenital nonspherocytic hemolytic anemia 1 trial · 12 incl. sub-types Sub-types →
- Congenital dyserythropoietic anemia 4 trials · 5 incl. sub-types Sub-types →
- Abetalipoproteinemia 2 trials
- Cutaneous porphyria 2 trials
- Hereditary spherocytosis 2 trials Sub-types →
- Southeast Asian ovalocytosis 2 trials
- Glycogen storage disease VII 1 trial
- Glycogen storage disease due to aldolase A deficiency 1 trial
- Rh deficiency syndrome 0 trials
- X-linked congenital hemolytic anemia 0 trials
- Cryohydrocytosis 0 trials
- Dehydrated hereditary stomatocytosis 2 0 trials
- Dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema 0 trials
- Elliptocytosis 1 0 trials
- Elliptocytosis 2 0 trials
- Familial pseudohyperkalemia 0 trials
- Hemolytic anemia due to diphosphoglycerate mutase deficiency 0 trials
- Hemolytic disease of fetus and newborn, RH-induced 0 trials
- Hereditary cryohydrocytosis with reduced stomatin 0 trials
- Overhydrated hereditary stomatocytosis 0 trials
- Primary CD59 deficiency 0 trials
- Renal tubular acidosis, distal, 4, with hemolytic anemia 0 trials
- Triosephosphate isomerase deficiency 0 trials
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Hereditary stomatocytosis 1 trial · 3 incl. sub-types
7 sub-types
- Southeast Asian ovalocytosis 2 trials
- Rh deficiency syndrome 0 trials
- Cryohydrocytosis 0 trials
- Dehydrated hereditary stomatocytosis 0 trials Sub-types →
- Familial pseudohyperkalemia 0 trials
- Hereditary cryohydrocytosis with reduced stomatin 0 trials
- Overhydrated hereditary stomatocytosis 0 trials
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Hereditary elliptocytosis 0 trials · 2 incl. sub-types
5 sub-types
- Southeast Asian ovalocytosis 2 trials
- Elliptocytosis 1 0 trials
- Elliptocytosis 2 0 trials
- Elliptocytosis 3 0 trials
- Hemolytic anemia with thermal sensitivity of red cells 0 trials
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Non-autoimmune hemolytic anemia 1 trial
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Heinz body anemia 0 trials
Most studied deeper sub-types
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Can a bispecific antibody tame two autoimmune blood disorders?
Disease control Not yet recruitingThis trial is testing an investigational drug called velinotamig in adults with immune thrombocytopenia (ITP) or warm autoimmune hemolytic anemia (wAIHA) that has relapsed or not responded to standard treatments. Velinotamig is an engineered bispecific antibody designed to target…
Phase 1/2 • Sponsor: Cullinan Therapeutics Inc. • Aim: Disease control
Last updated Aug 02, 2026 00:00 UTC
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Could vitamin c tame anemia? early trial tests high doses in rare blood disorders
Disease control Not yet recruitingThis early-stage study tests whether high-dose Vitamin C is safe for people with two rare inherited blood disorders—Pyruvate Kinase Deficiency (PKD) and a form of G6PD deficiency. Both conditions cause red blood cells to break down too quickly, leading to anemia. The study will e…
Phase 1 • Sponsor: University of Utah • Aim: Disease control
Last updated Jun 27, 2026 12:39 UTC