NDAORALCAPSULEPriority Review
Approved
Feb 2025
Lifecycle
Growth
Competitive Pressure
0/100
Clinical Trials
10
Data completeness
6/8 — Strong
Priority Review
GOMEKLI (mirdametinib) by SpringWorks Therapeutics is mitogen-activated protein kinase kinase 1 inhibitors [moa]. Approved for liposarcoma, neurofibromatosis type 1. First approved in 2025.
Drug data last refreshed 20h ago · AI intelligence enriched 2w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
GOMEKLI (mirdametinib) is an oral MEK1 inhibitor approved February 2025 for liposarcoma and neurofibromatosis type 1. It works by inhibiting mitogen-activated protein kinase kinase 1, a key driver of tumor cell proliferation in these rare cancers.
Growth18.4 years to LOE
Early-stage growth product with modest team size (7 linked jobs) offers opportunity to build commercial infrastructure in a rare disease franchise.
Mechanism of Action
Mitogen-Activated Protein Kinase Kinase 1 Inhibitors
Pharmacologic Class:
Kinase Inhibitor
Indications (2)
Clinical Trials (10)
A Study of Mirdametinib in People With Central Nervous System Tumors
Started Apr 2026
26 enrolled
Central Nervous System TumorsGlioma
To Assess the Enzyme Inducing Effects of Carbamazepine on the PK of Mirdametinib in Healthy Participants
Started Dec 2025
36 enrolled
HealthyVolunteer
Effect of Hepatic Impairment on the Pharmacokinetics of Mirdametinib
Started May 2025
32 enrolled
HealthyHepatic Impairment
A Study of Mirdametinib in Combination With Palbociclib in People With Liposarcoma
Started Feb 2025
54 enrolled
Well Differentiated LiposarcomaDedifferentiated LiposarcomaLiposarcoma+6 more
Mirdametinib Monotherapy in Adults With Neurofibromatosis 1 (NF1) and Cutaneous Neurofibromas (cNF).
Started Feb 2024
24 enrolled
NF1Cutaneous NeurofibromaMonotherapy
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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.