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MYOV News and Press, Myovant Sciences Ltd. From 04/12/21

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Company Name: Myovant Sciences Ltd.
Stock Symbol: MYOV
Market: NYSE
Website: myovant.com

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MYOV - Myovant Sciences and Pfizer Announce First Participant Dosed in Phase 3 SERENE Study Evaluating Contraceptive Efficacy of Once-Daily Relugolix Combination Tablet

SERENE is a Phase 3 single-arm, open-label study evaluating the contraceptive efficacy of investigational relugolix combination tablet in sexually active, healthy women ages 18-35 years Contraceptive potential of relugolix combination tablet supported by prior Phase 1 study that...

MYOV - Myovant Sciences names industry veteran as commercial chief

Myovant Sciences (MYOV) appointed Lauren Merendino as Chief Commercial Officer, effective today; she has 20+ years of pharmaceutical and biotech leadership experience.Most recently, she served as VP, Neurological Rare Diseases at Genentech."The recent FDA approval in advanced p...

MYOV - Myovant Sciences Appoints Lauren Merendino as Chief Commercial Officer

BASEL, Switzerland, April 05, 2021 (GLOBE NEWSWIRE) -- Myovant Sciences (NYSE: MYOV), a healthcare company focused on redefining care for women and for men, today announced the appointment of Lauren Merendino as Chief Commercial Officer of Myovant Sciences, Inc., effective April 5, 202...

MYOV - The 'Factor Zoo': Some Thoughts On 'Is There A Replication Crisis In Finance?'

A recent paper purports to show that academic research into factors is valid and that its results are replicable. I take a close look at the paper and read between the lines. I find that the authors' conclusions, while flawed, are valid and telling, and support the thesis that fac...

MYOV - Myovant Sciences Announces European Medicines Agency Validation of Marketing Authorization Application for Relugolix for the Treatment of Advanced Prostate Cancer

If approved, relugolix would be the first and only oral androgen deprivation therapy for advanced prostate cancer in Europe Relugolix is FDA-approved and currently available in the U.S. under the trade name ORGOVYX™ Pfizer has an exclusive option to commercializ...

MYOV - Pfizer, Myovant Sciences' relugolix combo shows positive action in uterine fibroids

Myovant Sciences (MYOV) and Pfizer (PFE) announce positive data from Phase 3 LIBERTY withdrawal study of relugolix combination therapy (relugolix 40 mg plus estradiol 1.0 mg and norethindrone acetate 0.5 mg) in women with uterine fibroids. The LIBERTY randomized withdrawal study met its prima...

MYOV - Myovant Sciences and Pfizer Announce Positive Data from Phase 3 LIBERTY Randomized Withdrawal Study of Once-Daily Relugolix Combination Therapy in Women with Uterine Fibroids

78.4% of women who continued on relugolix combination therapy remained responders (menstrual blood loss < 80 mL) through Week 76 compared with 15.1% of women who discontinued treatment at Week 52 (p < 0.0001) 69.8% of women who continued relugolix combination therapy remai...

MYOV - Myovant Sciences Announces Recipients of "Forward for Health Equity" Grants to Improve Healthcare Access in Prostate Cancer and Uterine Fibroids

BASEL, Switzerland, March 23, 2021 (GLOBE NEWSWIRE) -- Myovant Sciences (NYSE: MYOV), a healthcare company focused on redefining care for women and for men, today announced the four recipients of its Forward for Health Equity grants. The grant program provides funding to nonprofit heal...

MYOV - Myovant, Pfizer's relugolix combo shows durable efficacy in uterine fibroids

Myovant Sciences (MYOV) and Pfizer (PFE) announces publication of Phase 3 LIBERTY 1 and LIBERTY 2 studies of relugolix combination therapy (relugolix 40 mg plus estradiol 1.0 mg and norethindrone acetate 0.5 mg) in women with uterine fibroids in the New England Journal of Medicine.LIBERTY 1 a...

MYOV - Myovant Sciences and Pfizer Announce Publication in the New England Journal of Medicine of Phase 3 LIBERTY Studies of Once-Daily Relugolix Combination Therapy in Women with Uterine Fibroids

LIBERTY 1 and LIBERTY 2 achieved 73.4% and 71.2% response rates in menstrual blood loss, with an average reduction of 84.3% from baseline Achieved six of seven key secondary endpoints including reduction of pain Bone mineral density maintained at levels comparable to pla...

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