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  • Lenvima's PMS results for 6 years
  • by Lee, Hye-Kyung | translator Choi HeeYoung | Oct 25, 2022 05:45am
The incidence of abnormal cases is 93.94%
The Ministry of Food and Drug Safety's order to change the permission items will be inquired by the 3rd of next month
The permission of Lenvima, a thyroid-targeted anticancer drug, will be changed based on the results of a six-year post-marketing survey conducted in Korea. The Ministry of Food and Drug Safety will prepare a change order (proposal) based on the results of the post-marketing investigation of Lenvima by Eisai Korea and conduct an opinion inquiry by the 3rd of next month.

Lenvima treated patients with localized recurrent or metastatic progressive differentiated thyroid cancer who did not respond to radioactive iodine in October 2015. It obtained an item license in Korea for its effectiveness. Later, Lenvima's primary treatment for hepatocellular carcinoma and KIF5B-RET-positive lung adenocarcinoma clinical trials hav
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