Drug data last refreshed 2d ago · AI intelligence enriched 6d ago
MEKINIST (trametinib) is an oral small-molecule MEK inhibitor approved in March 2023 for treatment of BRAF-mutant melanoma and other solid tumors. It works by inhibiting mitogen-activated protein kinase (MEK) signaling, a critical pathway in cancer cell proliferation. The drug is administered as an oral solution, offering convenience for patients requiring targeted cancer therapy.
At peak lifecycle with $173M in Part D spending, the brand is likely in growth mode with established commercial infrastructure, though competitive pressure (8/10) suggests team focus on differentiation and market defense.
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
DETERMINE Trial Treatment Arm 07: Dabrafenib in Combination With Trametinib in Adult, Paediatric and Teenage/Young Adult Patients With BRAF V600 Mutation-Positive Cancers.
XP-102 and XP-102 in Combination With Trametinib in Advanced Solid Tumor Patients With a BRAF V600 Mutation
24VA021; VATCH Trametinib for Ras/MAPK Pathway VAs
Trametinib Plus Anlotinib Combined With Tislelizumab in KRAS-mutant NSCLC
A Study to Assess Naporafenib (ERAS-254) Administered With Trametinib in Patients With NRAS-mutant Melanoma (SEACRAFT-2)
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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/moLOE in ~5 years — strategic planning for patent cliff underway
$173M Medicare spend — this is a commercially significant brand
MEKINIST offers career opportunities in a peak-lifecycle oncology asset at a major pharma sponsor (Novartis) with substantial market presence ($173M Part D spending). Roles span commercial execution, medical affairs support, and competitive positioning in the high-pressure BRAF/MEK inhibitor space.