Generic Name |
Trametinib | |
---|---|---|
IND |
GSK1120212 | |
Brand Name (US) |
Mekinist | |
Manufacturer |
GlaxoSmithKline | |
Drug Type |
||
Delivery |
Oral | |
Approval Status |
Approved for a non-GIST cancer | |
Indications |
Melanoma, BRAF driven cancers | |
Overall Strategy |
||
Strategy |
Block related tumor signal paths | |
Drug Category |
MEK inhibitor |
Trametinib is a MEK1 and MEK2 inhibitor. It was approved by the FDA (USA) for use in BRAF mutated melanoma in January, 2014.
It is used as a single agent or in combination with dabrafenib for the treatment of patients with unresectable or metastatic melanoma with BRAF V600E or V600K mutations as detected by an FDA-approved test.
The recommended dosage regimens of MEKINIST are 2 mg orally once daily as a single agent or in combination with dabrafenib 150 mg orally twice daily. Take MEKINIST at least 1 hour before or at least 2 hours after a meal. See prescribing information.