Drug class

Antineoplastic - Protein-Tyrosine Kinase Inhibitors

Antineoplastic protein-tyrosine kinase inhibitors are a targeted therapeutic class of predominantly small-molecule agents designed to treat diverse malignancies. Read more about Antineoplastic - Protein-Tyrosine Kinase Inhibitors

170 drugs in this class 83 manufacturers

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Drugs in Antineoplastic - Protein-Tyrosine Kinase Inhibitors

Showing 37–45 of 170 drugs

IMATINIB MESYLATE

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

IMATINIB MESYLATE

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

ICLUSIG (ponatinib HCl)

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS · BLASTIC PHASE CHRONIC MYELOID LEUKEMIA ·+3
MILLENNIUM PHAR

ALUNBRIG (brigatinib)

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS · ANAPLASTIC LYMPHOMA KINASE POSITIVE NON-SMALL CELL LUNG CANCER
MILLENNIUM PHAR

ALUNBRIG (brigatinib)

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS · ANAPLASTIC LYMPHOMA KINASE POSITIVE NON-SMALL CELL LUNG CANCER
MILLENNIUM PHAR

VIZIMPRO (dacomitinib)

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS · METASTATIC NON-SMALL CELL LUNG CANCER WITH EGFR EXON 21 L858R SUBSTITUTION MUTATION ·+1
Parke-Davis Pfizer

LORBRENA (lorlatinib)

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS · ANAPLASTIC LYMPHOMA KINASE POSITIVE NON-SMALL CELL LUNG CANCER
Parke-Davis Pfizer

XOSPATA (gilteritinib fumarate)

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS · ACUTE MYELOID LEUKEMIA WITH FMS-LIKE TYROSINE KINASE-3 (FLT3) MUTATION
Astellas Pharma US

IMATINIB (imatinib mesylate)

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS · PHILADELPHIA CHROMOSOME POSITIVE ACUTE LYMPHOBLASTIC LEUKEMIA ·+11
ARMAS PHARMACEU
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About Antineoplastic - Protein-Tyrosine Kinase Inhibitors.

Antineoplastic protein-tyrosine kinase inhibitors are a targeted therapeutic class of predominantly small-molecule agents designed to treat diverse malignancies.

They function by competitively inhibiting the adenosine triphosphate (ATP)–binding sites or allosteric regulatory domains of receptor and non-receptor tyrosine kinases, thereby disrupting downstream intracellular signaling cascades essential for oncogenic cell proliferation, survival, and angiogenesis.

Clinically, these agents play a foundational role in managing both hematologic neoplasms, such as chronic myeloid leukemia, and a broad range of solid tumors, including non-small cell lung cancer, renal cell carcinoma, gastrointestinal stromal tumors, and breast cancer.