Indication

Philadelphia chromosome positive acute lymphoblastic leukemia

Philadelphia chromosome-positive acute lymphoblastic leukemia is an aggressive hematologic malignancy characterized by the malignant proliferation of immature lymphoid precursor cells, primarily of B-cell lineage, within the bone marrow and peripheral blood. Read more about Philadelphia chromosome positive acute lymphoblastic leukemia

45 drugs 38 manufacturers

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Drugs that treat it

Common Philadelphia chromosome positive acute lymphoblastic leukemia therapies.

Showing 1–9 of 45 drugs

GLEEVEC (imatinib mesylate)

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

SPRYCEL (dasatinib)

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS·PHILADELPHIA CHROMOSOME POSITIVE ACUTE LYMPHOBLASTIC LEUKEMIA·+4
BMS PRIMARYCARE

IMATINIB MESYLATE

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

IMATINIB MESYLATE

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

IMATINIB MESYLATE

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

IMATINIB MESYLATE

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

IMATINIB MESYLATE

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

IMATINIB MESYLATE

PHILADELPHIA CHROMOSOME POSITIVE ACUTE LYMPHOBLASTIC LEUKEMIA·+11
NORTHSTAR RX LL
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About Philadelphia chromosome positive acute lymphoblastic leukemia.

Philadelphia chromosome-positive acute lymphoblastic leukemia is an aggressive hematologic malignancy characterized by the malignant proliferation of immature lymphoid precursor cells, primarily of B-cell lineage, within the bone marrow and peripheral blood.

It is pathologically defined by the t(9;22)(q34;q11.2) reciprocal chromosomal translocation that creates the Philadelphia chromosome, generating the oncogenic BCR::ABL1 fusion gene and producing a constitutively active tyrosine kinase that drives dysregulated cell proliferation and survival.

While occurring in both pediatric and adult populations, its incidence increases markedly with age, representing roughly one-fourth of adult cases.

Patients typically present with systemic features of bone marrow failure, including anemia, thrombocytopenia, recurrent infections, fatigue, bleeding, and potential extramedullary involvement.

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