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Urovant Sciences and Pierre Fabre Médicament Enters into Exclusive License Agreement CI
Urovant Sciences Ltd. Presents New Data from EMPOWUR Study, Advancing Knowledge of the Treatment of Overactive Bladder at the 2022 American Urological Association Meeting CI
Urovant Sciences Presents Interim Data from Phase 2a Study of Investigational Novel Gene Therapy, URO-902, Supporting Safety, Tolerability, and Efficacy Endpoints CI
Urovant Sciences Announces the Publication of A New, Post-Hoc Analysis of Data from the Phase 3 EMPOWUR Trial of GEMTESA 75 Mg in the International Journal of Clinical Practice CI
Urovant Sciences Announces Management Changes CI
Urovant Sciences Ltd. Announces Executive Changes CI
Urovant Sciences Names Betzy Estrada as Executive VP and Chief Human Resources Officer CI
Urovant Sciences to Present Key Data for GEMTESA® 75 Mg At the 2021 Annual Meeting of the American Urological Association CI
Urovant Sciences Ltd.(NasdaqGS:UROV) dropped from S&P TMI Index CI
Urovant Sciences Ltd. Announces Board Changes CI
Urovant Sciences Ltd.(NasdaqGS:UROV) dropped from NASDAQ Composite Index CI
Sumitovant Biopharma Ltd. completed the acquisition of the remaining 27.6% stake in Urovant Sciences Ltd.. CI
Transcript : Urovant Sciences Ltd. - Shareholder/Analyst Call
Urovant Sciences : Posts Wider Fiscal Q3 Net Loss MT
Urovant Sciences Ltd. Reports Earnings Results for the Third Quarter Ended December 31, 2020 CI
Urovant Sciences : Safety Monitoring Board Recommends Phase 2a Trial of Urovant Sciences' URO-902 MT
Urovant Sciences Announces Progression of URO-902 Phase 2A Trial Following Positive Recommendation from the Data and Safety Monitoring Board CI
Urovant Sciences Ltd. Announces Amendments to Sumitomo Loan Agreement CI
Urovant Sciences : Gets FDA Nod For Overactive Bladder Drug Gemtesa -- Stock Up 3% After-Hours MT
Urovant Sciences Announces U.S. FDA Approval of GEMTESA 75 mg Tablets for the Treatment of Patients with Overactive Bladder CI
Urovant Sciences : Says Topline Data From Vibegron Study for Irritable Bowel Syndrome Failed to Meet Primary Endpoint MT
Urovant Sciences Reports Topline Data from the Phase 2A Clinical Trial Evaluating Once-Daily Vibegron 75 Mg CI
Urovant Sciences : Reports Positive Data From Study of Vibegron to Treat Overactive Bladder MT
Urovant Sciences Announces Positive Clinical Efficacy and Safety Data from Vibegron Empowur Long Term Extension Study CI
UROVANT SCIENCES : HC Wainwright Downgrades Urovant Sciences to Neutral From Buy; Price Target is $16.25 MT
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Urovant Sciences Ltd. is a biopharmaceutical company. The Company is focused on developing and commercializing therapies for a range of urologic conditions. The Company's lead product, GEMTESA (vibegron), is an oral, once-daily (75 mg) small molecule beta-3 agonist for the treatment of adult patients with overactive bladder (OAB) with symptoms of urge urinary incontinence, urgency, and urinary frequency. GEMTESA is also being evaluated for the treatment of OAB in men with benign prostatic hyperplasia. The Company's second product candidate, URO-902, is a gene therapy being developed for patients with OAB who have failed oral pharmacologic therapy.
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