Takeda to retry expanding all-comer coverage on Zejula
By Eo, Yun-Ho | translator Byun Kyung A
21.01.20 16:02:39
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Cancer Deliberation Committee to evaluate in January, expansion on PARP inhibitor to be noted
Efficacy approved based on Phase III PRIMA study, PFS reaches 13.8 months
The pharmaceutical industry insider reported the drug could not overcome the hurdle of the Health Insurance Review and Assessment Service (HIRA) Cancer Deliberation Committee in last June, but the poly ADP-ribose polymerase (PPARP) inhibitor Zejula¡¯s (niraparib), applied again in last August to expand the reimbursed indication. On Jan. 27, the Cancer Deliberation Committee would assess expanding the healthcare reimbursement on the drug¡¯s indication as a monotherapy for the patients with platinum-sensitive relapsed high grade serous epithelial ovarian, fallopian tube, or prim
Eo, Yun-Ho(unkindfish@dailypharm.com)
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