Drug class

Oral treatments for Non-Small Cell Lung Cancer

The phrase "oral treatments for non-small cell lung cancer" is not a formal or discrete pharmacological drug class recognized by regulatory agencies like the FDA or NCI, but rather an administrative grouping describing orally administered antineoplastic agents indicated for non-small cell lung cancer. Read more about Oral treatments for Non-Small Cell Lung Cancer

42 drugs in this class 30 manufacturers

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Drugs in Oral treatments for Non-Small Cell Lung Cancer

Showing 10–18 of 42 drugs

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

ERLOTINIB (erlotinib HCl)

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS · ADENOCARCINOMA OF PANCREAS ·+2
SUN PHARMACEUTI

ERLOTINIB (erlotinib HCl)

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS · ADENOCARCINOMA OF PANCREAS ·+2
MYLAN INSTITUTI

ERLOTINIB (erlotinib HCl)

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS · ADENOCARCINOMA OF PANCREAS ·+2
ARMAS PHARMACEU

ZYKADIA (ceritinib)

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

TABRECTA (capmatinib hydrochloride)

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS · NON-SMALL CELL LUNG CANCER WITH MESENCHYMAL-EPITHELIAL TRANSITION (MET) EXON 14 SKIPPING
Novartis Pharmaceuticals
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About Oral treatments for Non-Small Cell Lung Cancer.

The phrase "oral treatments for non-small cell lung cancer" is not a formal or discrete pharmacological drug class recognized by regulatory agencies like the FDA or NCI, but rather an administrative grouping describing orally administered antineoplastic agents indicated for non-small cell lung cancer.

This broad category predominantly comprises small-molecule targeted therapies—principally tyrosine kinase inhibitors and related molecular inhibitors targeting alterations such as EGFR, ALK, ROS1, BRAF, RET, MET, KRAS, and HER2—as well as select oral chemotherapeutic agents.

These agents function mechanistically by selectively disrupting intracellular oncogenic signaling cascades or inhibiting cell division to arrest tumor proliferation and induce apoptosis.

Clinically, they are used across early-stage adjuvant, locally advanced, and metastatic non-small cell lung cancer regimens matching specific genomic or clinical profiles.