COMPOSITION:
Each film-coated tablet contains Erdafitinib …………4 mg
INDICATION:
LuciErda is a kinase inhibitor indicated for the treatment of adult patients with locally advanced or metastatic urothelial carcinoma (mUC) that has
• susceptible FGFR3 or FGFR2 genetic alterations and
• progressed during or following at least one line of prior platinum-containing chemotherapy including within 12 months of neoadjuvant or adjuvant platinum-containing chemotherapy.
DOSAGE AND USE:
• Confirm the presence of FGFR genetic alterations in tumor specimens prior to initiation of treatment with LuciErda.
• Recommended initial dosage: 8 mg orally once daily with a dose increase to 9 mg daily if criteria are met.
• Swallow whole with or without food.
STORAGE:
in a dry place and store at 20°C to 25°C.
MANUFACTURED AND MARKETED BY:
LUCIUS PHARMACEUTICALS(LAO) CO., LTD
No.26, Thongmang village, Xaythany district, Vientiane Capital, Laos
WARNING:
Keep medicine out of reach of Children. Do not administer LuciErda during Pregnancy and Lactation.
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