Max Gelman
Associate Editor
Christmas has come early for Urovant Sciences as the former Vivek Ramaswamy outfit scored an FDA approval for its lead program.
James Robinson
The biotech’s overactive bladder candidate vibegron will be the newest drug to hit the market, the agency said Wednesday, giving Urovant its first approved product. Vibegron, a beta-3 agonist that’s taken as a once-daily pill, will be sold as Gemtesa. The drug is likely to launch in early 2021, CEO James Robinson has previously said.
The FDA based Gemtesa’s approval on data from a Phase III trial that raised nearly as many questions as it answered back in March 2019. The drug hit both co-primary endpoints and seven secondary endpoints compared with placebo after three months of treatment and a one-month safety follow-up. Gemtesa cut average instances of incontinence every 24 hours by 2 from a baseline of 3.43, achieving a clear win over the 1.4 drop in the placebo arm.
But Urovant tested the drug alongside a cheap generic called tolterodine, which also achieved statistical significance over placebo at a 1.8 drop from baseline, coming close to Gemtesa’s results. Researchers said at the time that even though vibegron achieved “numerically better efficacy than tolterodine,” they did not run a p-value for the Urovant drug against the generic.
That left analysts to make the comparisons on their own and sent Urovant’s stock price down 17% after an initial 20% spike. Ramaswamy originally bagged the drug in a small $25 million deal from Merck, and it’s one of multiple drugs he predicted would reach approval by 2022.
It’s a big win for the biotech, coming just over a month after its parent company, a subsidiary of Sumitomo Dainippon, bought Urovant out in full to bring the biotech closer into its own network of companies and former Vants.
Urovant was acquired for $584 million in an all-cash deal, valuing the biotech at $16.25 per share. The figure represented a 96% premium on the biotech’s closing price a day earlier, and the timing proved fruitful given Wednesday’s announcement.
Vivek Ramaswamy
Focusing on urinary diseases, Urovant was one of five biotech Ramaswamy sold to Sumitomo Dainippon about 15 months ago. The group included Myovant, which last week saw an approval of its own in prostate cancer; Enzyvant (pediatric rare diseases); Altavant (respiratory rare diseases) and Spirovant (pulmonary diseases). Ramaswamy brought in $3 billion with the move, and it included the option of buying another 6 of his startups.
Ramaswamy also remains on the board of Sumitovant, the ex-Vant umbrella owned by Sumitomo Dainippon.
The company is further evaluating vibegron in OAB in men with benign prostatic hyperplasia and for abdominal pain associated with irritable bowel syndrome. Further down the pipeline, Urovant has a gene therapy program called hMaxi-K, which is being researched for patients with OAB symptoms who have failed oral pharmacologic therapy.
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