Indication

Chronic eosinophilic leukemia

Chronic eosinophilic leukemia is a rare myeloproliferative neoplasm characterized by the autonomous, clonal overproduction of eosinophils within the bone marrow, peripheral blood, and tissues. Read more about Chronic eosinophilic leukemia

28 drugs 27 manufacturers

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Drugs that treat it

Common Chronic eosinophilic leukemia therapies.

Showing 19–27 of 28 drugs

IMATINIB MESYLATE

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS·PHILADELPHIA CHROMOSOME POSITIVE ACUTE LYMPHOBLASTIC LEUKEMIA·+11
AHP

IMATINIB MESYLATE

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS·PHILADELPHIA CHROMOSOME POSITIVE ACUTE LYMPHOBLASTIC LEUKEMIA·+11
AUROBINDO PHARM

IMATINIB MESYLATE

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS·PHILADELPHIA CHROMOSOME POSITIVE ACUTE LYMPHOBLASTIC LEUKEMIA·+11
ARMAS PHARMACEU

IMKELDI (imatinib mesylate)

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS·PHILADELPHIA CHROMOSOME POSITIVE ACUTE LYMPHOBLASTIC LEUKEMIA·+11
SHORLA PHARMA I

IMATINIB MESYLATE

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS·PHILADELPHIA CHROMOSOME POSITIVE ACUTE LYMPHOBLASTIC LEUKEMIA·+11
QUALLENT PHARMA

IMATINIB MESYLATE

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS·PHILADELPHIA CHROMOSOME POSITIVE ACUTE LYMPHOBLASTIC LEUKEMIA·+11
BLUEPOINT/ONCOP

IMATINIB MESYLATE

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS·PHILADELPHIA CHROMOSOME POSITIVE ACUTE LYMPHOBLASTIC LEUKEMIA·+11
CAMBER PHARMACE

GLEEVEC (imatinib mesylate)

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS·PHILADELPHIA CHROMOSOME POSITIVE ACUTE LYMPHOBLASTIC LEUKEMIA·+11
Novartis Pharmaceuticals

IMATINIB MESYLATE

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS·PHILADELPHIA CHROMOSOME POSITIVE ACUTE LYMPHOBLASTIC LEUKEMIA·+11
SAFECOR HEALTH
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About Chronic eosinophilic leukemia.

Chronic eosinophilic leukemia is a rare myeloproliferative neoplasm characterized by the autonomous, clonal overproduction of eosinophils within the bone marrow, peripheral blood, and tissues.

Primarily affecting adults, the disease involves persistent hypereosinophilia accompanied by cytogenetic abnormalities, somatic driver mutations, or elevated blast counts, while excluding reactive causes and distinct myeloid neoplasms defined by rearrangements such as *PDGFRA*, *PDGFRB*, *FGFR1*, or *PCM1::JAK2*.

Widespread infiltration of tissues by mature and immature eosinophils releases cytotoxic granules, commonly causing organ dysfunction and damage across the cardiovascular system, central nervous system, lungs, skin, and gastrointestinal tract.

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