ALUNBRIG (brigatinib) by Takeda is tyrosine kinase inhibitors [moa]. Approved for kinase inhibitor [epc]. First approved in 2017.
Drug data last refreshed 20h ago · AI intelligence enriched 3w ago
ALUNBRIG (brigatinib) is an oral small-molecule tyrosine kinase inhibitor developed by Takeda and approved by the FDA on April 28, 2017. It is indicated for the treatment of patients with anaplastic lymphoma kinase (ALK)-positive non-small cell lung cancer. The drug works by inhibiting tyrosine kinase activity, disrupting cancer cell proliferation and survival pathways. ALUNBRIG serves as a treatment option for ALK-positive NSCLC patients, particularly those with resistance to crizotinib or other first-generation ALK inhibitors.
Tyrosine Kinase Inhibitors
Kinase Inhibitor
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
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Upgrade to Pro — $25/moALUNBRIG supports specialized oncology-focused commercial roles including product managers, medical science liaisons, and specialty sales representatives targeting pulmonology and oncology practices. Success in this role requires deep knowledge of ALK biology, NSCLC treatment algorithms, and ability to differentiate within a competitive kinase inhibitor market. Currently, zero open positions are linked to ALUNBRIG in available job tracking data.