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Urovant Sciences Announces Publication of New Review of Efficacy and Safety Data for GEMTESA® (vibegron) 75 mg in Overactive Bladder Patients in the Journal Therapeutics and Clinical Risk Management
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Urovant Sciences Announces Positive Topline Results of Phase 2a Trial of its Potential Novel Gene Therapy, URO-902
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Myovant Sciences (MYOV) Receives Positive CHMP Opinion for ORGOVYX® (relugolix) for the Treatment of Advanced Prostate Cancer
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Myovant Sciences Receives Positive CHMP Opinion for ORGOVYX® (relugolix) for the Treatment of Advanced Prostate Cancer
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Myovant Sciences Receives Positive CHMP Opinion for ORGOVYX® (relugolix) for the Treatment of Advanced Prostate Cancer
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Myovant Sciences to Present at Upcoming Investor Conferences
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Myovant Sciences to Present at Upcoming Investor Conferences
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Myovant Sciences Announces Financial Results for Third Quarter of Fiscal Year 2021 and Corporate Updates
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Myovant Sciences Announces Financial Results for Third Quarter of Fiscal Year 2021 and Corporate Updates
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Myovant Sciences to Host Third Fiscal Quarter 2021 Earnings Conference Call at 8:30 a.m. Eastern Time on January 26, 2022
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Myovant Sciences to Host Third Fiscal Quarter 2021 Earnings Conference Call at 8:30 a.m. Eastern Time on January 26, 2022
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Myovant Sciences (MYOV) Reports Prelim Q3 Results
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Myovant Sciences Announces Preliminary Financial Results for Third Quarter of Fiscal Year 2021
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Myovant Sciences to Present at the 40th Annual J.P. Morgan Healthcare Conference
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Myovant Sciences to Present at the 40th Annual J.P. Morgan Healthcare Conference
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Urovant Sciences Announces Publication in Advances in Therapy of Analyses of Patient-Perceived Meaningfulness of Improvement in Symptom Reduction for Overactive Bladder Patients Treated with GEMTESA®
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Sumitovant Biopharma Highlights Significant Clinical, Regulatory and Commercial Achievements Across its Portfolio of Companies in the Second Quarter of FY2021
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Myovant Sciences to Participate in the Evercore ISI 4th Annual HealthCONx Conference
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Myovant Sciences to Participate in the Evercore ISI 4th Annual HealthCONx Conference
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Urovant Sciences Announces Publication in Blood Pressure Monitoring of Positive Ambulatory Blood Pressure Study Results for GEMTESA® (vibegron) 75 mg in Overactive Bladder Patients
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Myovant Sciences (MYOV) Appoints Nancy Valente to its Board
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Nancy Valente, M.D. Joins Myovant Sciences’ Board of Directors
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Nancy Valente, M.D. Joins Myovant Sciences’ Board of Directors
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Spirovant Presents Preclinical Data Showing SP-101 Restores CF Transmembrane Conductance Regulator Function at the 2021 North American Cystic Fibrosis Conference
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Myovant Sciences Announces Financial Results for Second Quarter of Fiscal Year 2021 and Corporate Updates
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Myovant Sciences (MYOV) and Pfizer (PFE) Report Data on Relugolix Combination Therapy from Studies in Uterine Fibroids and Endometriosis
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Myovant Sciences and Pfizer Present Data on Relugolix Combination Therapy from Studies in Uterine Fibroids and Endometriosis at the American Society for Reproductive Medicine Congress
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Myovant Sciences and Pfizer Present Data on Relugolix Combination Therapy from Studies in Uterine Fibroids and Endometriosis at the American Society for Reproductive Medicine Congress
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Myovant Sciences to Host Second Fiscal Quarter 2021 Earnings Conference Call at 8:30 a.m. Eastern Time on October 26, 2021
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Myovant Sciences to Host Second Fiscal Quarter 2021 Earnings Conference Call at 8:30 a.m. Eastern Time on October 26, 2021
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Enzyvant Receives FDA Approval for RETHYMIC® (allogeneic processed thymus tissue-agdc), a One-Time Regenerative Tissue-Based Therapy for Pediatric Congenital Athymia
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Enzyvant Receives FDA Approval for RETHYMIC® (allogeneic processed thymus tissue-agdc), a One-Time Regenerative Tissue-Based Therapy for Pediatric Congenital Athymia
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Myovant Sciences (MYOV), Pfizer (PFE) Announce FDA Acceptance of sNDA for MYFEMBREE for Management of Moderate to Severe Pain Associated With Endometriosis
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Myovant Sciences and Pfizer Announce FDA Acceptance of Supplemental New Drug Application for MYFEMBREE® for the Management of Moderate to Severe Pain Associated With Endometriosis
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Myovant Sciences and Pfizer Announce FDA Acceptance of Supplemental New Drug Application for MYFEMBREE® for the Management of Moderate to Severe Pain Associated With Endometriosis
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Myovant Sciences to Participate in the 2021 Baird Global Healthcare Conference
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Myovant Sciences to Participate in the 2021 Baird Global Healthcare Conference
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Enzyvant Announces First-Ever Data on Burden of Illness and Costs of Supportive Care for Pediatric Congenital Athymia
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Enzyvant Announces First-Ever Data on Burden of Illness and Costs of Supportive Care for Pediatric Congenital Athymia
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Myovant Sciences (MYOV) Appoints Uneek Mehra as Chief Financial and Business Officer
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Myovant Sciences Appoints Uneek Mehra as Chief Financial and Business Officer
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Myovant Sciences Appoints Uneek Mehra as Chief Financial and Business Officer
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Enzyvant Announces Publication of Positive Clinical Data in Pediatric Patients with Congenital Athymia Treated with Investigational RVT-802 (allogeneic processed thymus tissue-agdc)
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Enzyvant Announces Publication of Positive Clinical Data in Pediatric Patients with Congenital Athymia Treated with Investigational RVT-802 (allogeneic processed thymus tissue-agdc)
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Myovant Sciences Announces Financial Results for First Quarter of Fiscal Year 2021 and Corporate Updates
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Myovant Sciences Announces European Commission Approval for RYEQO® for the Treatment of Women With Uterine Fibroids
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Myovant Sciences Announces European Commission Approval for RYEQO® for the Treatment of Women With Uterine Fibroids
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Myovant Sciences to Host First Fiscal Quarter 2021 Earnings Conference Call at 8:30 a.m. Eastern Time on July 28, 2021
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Myovant Sciences to Host First Fiscal Quarter 2021 Earnings Conference Call at 8:30 a.m. Eastern Time on July 28, 2021
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Myovant Sciences to Present at Upcoming Investor Conferences

