Ardelyx (ARDX) Presents Positive Penapanor Phase 2b Endpoint Data in IBS-C Patients

October 19, 2016 7:08 AM EDT

Get access to the best calls on Wall Street with's Ratings Insider Elite. Get your Free Trial here.

Ardelyx, Inc. (Nasdaq: ARDX) announced the presentation of positive global endpoint data from its Phase 2b trial, completed in September 2014, which evaluated tenapanor for the treatment of patients with irritable bowel syndrome with constipation (IBS-C). These pre-specified analyses build off of positive efficacy findings on the study's primary and key secondary endpoints in the same patient population, as previously announced in October 2014 and presented at Digestive Disease Week in 2015. They also further validate the 50 milligram (mg), twice-daily dose of tenapanor chosen for the two ongoing Phase 3 studies, T3MPO-1 and T3MPO-2, in patients with IBS-C, which are expected to have data readouts in mid- and late-2017, respectively. The company is also evaluating tenapanor in a Phase 3 study for the treatment of hyperphosphatemia in end-stage renal disease (ESRD) patients on dialysis, with data expected to be reported in the first quarter of 2017.

William D. Chey, M.D., the Timothy T. Nostrant professor of gastroenterology at the University of Michigan Health System, will present these secondary endpoint findings in an oral session today during the American College of Gastroenterology (ACG) Annual Scientific Meeting and Post Graduate Course.

"In this methodologically rigorous Phase 2b trial, 50 mg of tenapanor twice a day provided robust benefits for the key symptoms of IBS-C, including abdominal pain and stool frequency, compared to placebo," said Dr. Chey. "The results of this trial laid the groundwork for the ongoing Phase 3 clinical trials of tenapanor in patients with IBS-C. I eagerly await results of these trials and hope that tenapanor's unique mechanism of action will expand the list of options available to treat patients with IBS-C."

The IBS symptom global endpoints in the Phase 2b study included: adequate IBS symptom relief; improvements in IBS severity, constipation severity and treatment satisfaction. Compared to placebo, treatment with 50 mg of tenapanor twice a day resulted in statistically significant improvements in all global endpoints measured. Notably, 63.1 percent of patients treated with 50 mg of tenapanor twice a day reported adequate relief of IBS symptoms compared to 39.3 percent for patients on placebo (p = 0.002).

Additional clinically meaningful and statistically significant improvements with tenapanor 50 mg twice-daily dosing compared with placebo included reduction in IBS severity (p = 0.024); reduction in constipation severity (p < 0.001); increased mean satisfaction score (p < 0.001); and, improvement in the degree of IBS symptom relief (p < 0.001).

"IBS-C significantly impacts the quality of life of millions of people, but there are few, effective treatment options today," said Mike Raab, president and chief executive officer, Ardelyx. "These data further demonstrate the potential for tenapanor to effectively improve critical clinical symptoms in patients with IBS-C, and represent an important perspective for clinicians in evaluating patients' satisfaction and tolerability when treating with tenapanor. We look forward to sharing results from the Phase 3 trials throughout 2017 and believe that tenapanor's unique mechanism of action will provide a differentiated option for those affected by IBS-C."

Presentation Details

Title: The Effect of Tenapanor on Global Endpoints in Patients with Constipation Predominant Irritable Bowel Syndrome: Results from a 12-Week, Double-Blind, Placebo-Controlled, Randomized Phase 2b Trial Date: Wednesday, October 19, 2016Time: 8:30 a.m. – 8:40 a.m. PDTLocation: The Venetian Hotel, Las Vegas, NVRoom: Venetian Ballroom E

Serious News for Serious Traders! Try Premium Free!

You May Also Be Interested In

Related Categories

Corporate News, FDA

Add Your Comment