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Myovant Sciences and Pfizer Provide Update on Supplemental

BASEL, Switzerland and NEW YORK, April 12, 2022 (GLOBE NEWSWIRE) Myovant Sciences (NYSE: MYOV) and Pfizer (NYSE: PFE) announced today an update on the. ....

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Myovant Sciences and Pfizer Present Data on Relugolix

BASEL, Switzerland and NEW YORK, Oct. 19, 2021 (GLOBE NEWSWIRE) Myovant Sciences (NYSE: MYOV) and Pfizer Inc. (NYSE: PFE) today announced the. ....

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Myovant Sciences and Pfizer Receive FDA Approval for

In the Phase 3 LIBERTY 1 and LIBERTY 2 studies, MYFEMBREE demonstrated 72.1% and 71.2% response rates in menstrual blood loss (MBL) at Week 24, with MBL. ....

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Pfizer And Myovant Get FDA Nod For Myfembree

Pfizer And Myovant Get FDA Nod For Myfembree
NEW YORK CITY (dpa-AFX) - Pfizer Inc. and Myovant Sciences announced that the U.S. Food and Drug Administration has approved Myfembree, the first once-daily treatment for heavy menstrual bleeding associated with uterine fibroids.
Under the collaboration terms, Myovant and Pfizer will jointly commercialize Myfembree (relugolix 40 mg, estradiol 1 mg, and norethindrone acetate 0.5 mg) in the U.S. The drug is expected to be available in June 2021.
Myfembree is approved for management of heavy menstrual bleeding associated with uterine fibroids in premenopausal women, with a treatment duration of up to 24 months. Uterine fibroids are noncancerous tumors that develop in or on the muscular walls of the uterus. It is a chronic and debilitating disease for many women in the U.S. ....

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Myovant Sciences Says FDA Places Phase 3 SERENE Study On Partial Clinical Hold

NEW YORK CITY (dpa-AFX) - Myovant Sciences Ltd. (MYOV) said the Food and Drug Administration has placed a partial clinical hold on the Phase 3 SERENE study of its relugolix combination tablet proposed ....

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