Pemigatinib

Another Name
pemigatinib、佩米替尼、达伯坦
Indications
Used for the treatment of advanced, unresectable cholangiocarcinoma with FGFR2 gene fusion or rearrangement.
Reg No
07 L 0997/23
Inspection No
1764-23
dosage form:tablet
Specs:4.5mg
Indate:24 months
Date:2024-9-1 Views:1096

COMPOSITION:

Each LuciPem tablet contains: Pemigatinib 4.5mg

INDICATION:

LuciPem is a kinase inhibitor indicated for the treatment of adults with previously treated, unresectable locally advanced or metastatic cholangiocarcinoma with a fibroblast growth factor receptor 2 (FGFR2) fusion or other rearrangement as detected by an FDA-approved test.

DOSAGE AND USE:

Recommended dosage is 13.5 mg orally once daily for 14 consecutive days followed by 7 days off therapy in 21-day cycles. Continue treatment until disease progression or unacceptable toxicity occurs.

Severe Renal/Hepatic impairment: the recommended dosage of LuciPem is 9 mg orally once daily for 14 consecutive days followed by 7 days off therapy in 21-day cycles.

Tablets should be swallowed whole & not chewed or crushed.

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 the reach of Children. Do not administered LuciPem in Pregnancy and

Lactation patient treatment.

Original article, if reprinted, please indicate the link to this article: https://lucius-pharmaceuticals.com/drug/pemigatinib/

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