Description
Trametinib
Each Tablet contains: 2.254 mg Trametinib dimethyl sulfoxide equivalent to Trametinib. … 2mg
INDICATION
LuciTram is a kinase inhibitor indicated as a single agent for the treatment of BRAF-inhibitor treatment-naïve patients with unresectable or metastatic melanoma with BRAF V600E or V600K mutations. LuciTram is indicated, in combination with dabrafenib, for: • The treatment of patients with unresectable or metastatic melanoma with BRAF V600E or V600K mutations. • The adjuvant treatment of patients with melanoma with BRAF V600E or V600K mutations. • The treatment of patients with metastatic non -small cell lung cancer (NSCLC) with BRAF V600E mutation. • The treatment of patients with locally advanced or metastatic anaplastic thyroid cancer • (ATC) with BRAF V600E mutation and with no satisfactory locoregional treatment options.
DOSAGE AND USE
The recommended dosage of LuciTram is 2 mg orally once daily. Take LuciTram at least 1 hour before or at least 2 hours after a meal. Tablet should be swallowed whole & not chewed or crushed.
STORAGE
In a dry place and store at 2°C to 8°C.
MANUFACTURED AND MARKETED BY
LUCIUS PHARMACEUTICALS(LAO) CO., LTD. No.26, Thongmang village, Xaythany district, Vientiane Capital, Laos
WARNING
Keep medicine out of the reach of Children. Do not administered LuciTram in Pregnancy and Lactation.




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