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Friday, August 2, 2019

FDA OKs Daiichi’s pexidartinib for rare synovial cancer

The FDA approves Daiichi Sankyo’s (OTCPK:DSNKY +0.2%) Turalio (pexidartinib) for the treatment of adult patients with symptomatic tenosynovial giant cell tumor (TGCT) associated with severe morbidity or functional limitations that cannot be improved with surgery.
TGCT is a rare benign cancer that occurs in the synovium, bursae and tendon sheath. Synovium is the thin membrane that covers the surface of joint spaces.
Small molecule pexidartinib inhibits a cell surface protein called colony stimulating factor-1 receptor (CSF1R) which is the primary growth driver of abnormal cells in the synovium.

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