| 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.