Drug class

Antineoplastic - Anaplastic Lymphoma Kinase (ALK) Inhibitors

Antineoplastic anaplastic lymphoma kinase (ALK) inhibitors are a targeted therapeutic class of small-molecule tyrosine kinase inhibitors designed to selectively block oncogenic ALK signaling. Read more about Antineoplastic - Anaplastic Lymphoma Kinase (ALK) Inhibitors

11 drugs in this class 8 manufacturers

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Drugs in Antineoplastic - Anaplastic Lymphoma Kinase (ALK) Inhibitors

Showing 1–9 of 11 drugs

XALKORI (crizotinib)

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS · ANAPLASTIC LYMPHOMA KINASE POSITIVE NON-SMALL CELL LUNG CANCER ·+3
Parke-Davis Pfizer

ZYKADIA (ceritinib)

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS · ANAPLASTIC LYMPHOMA KINASE POSITIVE NON-SMALL CELL LUNG CANCER
Novartis Pharmaceuticals

ALECENSA (alectinib HCl)

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

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

LORBRENA (lorlatinib)

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

ZYKADIA (ceritinib)

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS · ANAPLASTIC LYMPHOMA KINASE POSITIVE NON-SMALL CELL LUNG CANCER
Novartis Pharmaceuticals

XALKORI (crizotinib)

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS · ANAPLASTIC LYMPHOMA KINASE POSITIVE NON-SMALL CELL LUNG CANCER ·+3
Laboratories Div
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About Antineoplastic - Anaplastic Lymphoma Kinase (ALK) Inhibitors.

Antineoplastic anaplastic lymphoma kinase (ALK) inhibitors are a targeted therapeutic class of small-molecule tyrosine kinase inhibitors designed to selectively block oncogenic ALK signaling.

By binding to the ATP-binding pocket of the ALK receptor kinase, these agents disrupt constitutive phosphorylation and shut down downstream oncogenic cascades—such as the STAT3, AKT, and MAPK pathways—that promote malignant cell proliferation and survival.

Therapeutically, this class is primarily indicated for patients with locally advanced or metastatic non-small cell lung cancer harboring an ALK rearrangement.

Select agents within the class also have approved roles or established utility in other ALK-driven malignancies, including relapsed or refractory systemic anaplastic large-cell lymphoma and unresectable inflammatory myofibroblastic tumors.