NDAORALTABLET
Approved
May 2013
Lifecycle
Peak
Competitive Pressure
0/100
Clinical Trials
20
Data completeness
4/8 — Partial
Drug data last refreshed 12h ago · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
MEKINIST (trametinib) is an oral small-molecule MEK inhibitor approved by the FDA in May 2013 for treating 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 often used as monotherapy or in combination with BRAF inhibitors to enhance efficacy.
$173MPart D
Peak7.4 years to LOEPeak-stage product with $173M in Part D spending demonstrates strong market presence and stable commercial team supporting oncology portfolio.
Mechanism of Action
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (20)
DETERMINE Trial Treatment Arm 07: Dabrafenib in Combination With Trametinib in Adult, Paediatric and Teenage/Young Adult Patients With BRAF V600 Mutation-Positive Cancers.
Started Apr 2026
30 enrolled
Haematological MalignancyMalignant NeoplasmLymphoproliferative Disorders+17 more
XP-102 and XP-102 in Combination With Trametinib in Advanced Solid Tumor Patients With a BRAF V600 Mutation
Started Dec 2025
221 enrolled
CancerBRAF V600 MutationMelanoma+3 more
24VA021; VATCH Trametinib for Ras/MAPK Pathway VAs
Started Aug 2025
45 enrolled
Ras/MAPK Pathway Vascular AnomaliesVascular AnomaliesVascular Anomaly
Trametinib Plus Anlotinib Combined With Tislelizumab in KRAS-mutant NSCLC
Started Jul 2024
60 enrolled
KRAS Mutation-Related TumorsAdvanced Lung CancerRefractory Tumor
A Study to Assess Naporafenib (ERAS-254) Administered With Trametinib in Patients With NRAS-mutant Melanoma (SEACRAFT-2)
Started Apr 2024
78 enrolled
Advanced or Metastatic NRAS-mutant Melanoma
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
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.