Improving quality-of-life through innovations in urology.
Urovant Sciences is a clinical-stage biopharmaceutical company focused on developing and commercializing innovative therapies for urologic conditions. Urovant is a nimble company with an entrepreneurial focus on improving the way providers and their patients confront urologic diseases that are difficult to treat.
Every employee at Urovant plays an integral role to our success. We are ambitious in our approach to improving outcomes for the patients and healthcare providers we serve. Our fast-paced environment rewards strategic decision-making and collaboration, giving team members opportunities to grow beyond their expertise.
Urovant's lead product candidate, vibegron, is a β3-adrenergic agonist being developed for an oral, once-daily treatment for overactive bladder with symptoms of urge urinary incontinence, urgency, and urinary frequency.
Urovant's second investigational product candidate, hMaxi-K, is a novel gene therapy for patients with overactive bladder symptoms who have failed oral pharmacologic therapy.
Overactive bladder (OAB) is a clinical condition characterized by the sudden urge to urinate, with or without accidental urinary leakage, and usually with increased frequency. The exact cause is unknown, making this a difficult condition to treat. In the United States, more than 30 million people over the age of 40 suffer from the bothersome symptoms of OAB1, which can lead to depression and anxiety and have a negative impact on quality of life.2
- Coyne, et al., EpiLUTS 2007
- Kinsey D, et al., J Health Psychol. 2016
Trust. Collaboration. Accountability. Expertise. Integrity. Every employee at Urovant plays an integral role to our success. We are ambitious in our approach to improving outcomes for the patients and healthcare providers we serve. Our fast-paced environment rewards strategic decision making and collaboration. Our team members have opportunities to grow beyond their expertise.
Join us at the Fall 2018 Biotech Bay & Genetown Talent Connect.
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Develop and execute global Investor Relations program that accurately reflects the company’s performance, vision, and strategy
Lead newly created managed markets function prior to launch.
Oversee the quality aspects of Clinical and Chemistry, Manufacturing, Controls (CMC).
Lead biologics pharmaceutical development for h-Maxi K, a novel gene therapy, and manage clinical trial supplies across multiple clinical studies.