Healthcare firm Roivant Sciences has formed a new subsidiary known as 鈥楿rovant Sciences鈥� to develop new therapies for addressing urologic conditions.

Urovant has licensed global rights, except in certain Asian countries such as Japan, to develop and commercialise a therapeutic candidate called vibegron from Merck Sharp & Dohme.

Go deeper with GlobalData

  • ReportsLogo

  • ReportsLogo

Data Insights

The gold standard of business intelligence.

Find out more

Related Company Profiles

Vibegron is an oral 尾3-adrenergic agonist currently being developed to treat patients with an that is characterised by symptoms of urge urinary incontinence, urgency and urinary frequency.

The 尾3-adrenergic receptor is said to play a role in the bladder fill-void cycle, and by inducing the pathway, vibegron is expected to relax the bladder detrusor muscle and allow efficient storage of urine.

Roivant Sciences founder and CEO Vivek Ramaswamy said: “Urologic conditions such as overactive bladder adversely impact millions of individuals, and the current treatment options are unsatisfactory for many patients.

“Our aim is to provide patients with better options as quickly as possible.”

鈥淥ur aim is to provide patients with better options as quickly as possible.”

How well do you really know your competitors?

Access the most comprehensive Company Profiles on the market, powered by GlobalData. Save hours of research. Gain competitive edge.

Company Profile 鈥� free sample

Thank you!

Your download email will arrive shortly

Not ready to buy yet? Download a free sample

We are confident about the unique quality of our Company Profiles. However, we want you to make the most beneficial decision for your business, so we offer a free sample that you can download by submitting the below form

By GlobalData
Visit our for more information about our services, how we may use, process and share your personal data, including information of your rights in respect of your personal data and how you can unsubscribe from future marketing communications. Our services are intended for corporate subscribers and you warrant that the email address submitted is your corporate email address.

The product is undergoing evaluation for safety and efficacy in more than 2,700 patients with symptoms of overactive bladder.

Vibegron was reported to have met the primary and key secondary endpoints in a randomised, double-blind, placebo-controlled and active comparator-controlled Phase IIb clinical trial conducted in more than 1,300 subjects.

A randomised, placebo and active comparator-controlled Phase III trial of more than 1,000 patients also met its required endpoints.

In the coming months, Urovant intends to initiate a multinational Phase III registration programme for vibegron.