Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
BUSINESS
FDA Defers PDUFA Date for Myfembree for Endometriosis Use: Myovant/Pfizer
The US FDA has extended the review period for Myfembree (relugolix + estradiol + norethindrone acetate) for an additional endometriosis indication, Myovant Sciences, a subsidiary of Sumitomo Pharma, and US partner Pfizer said on May 9. The US regulator has…
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