Bellerophon's stock tanks as inhaled drug-device fails to redeem itself in new PhIII after previous flops
In the five years since Bellerophon Therapeutics’ only program, a device for administering inhaled nitric oxide called INOpulse, flunked its first Phase III study, the New Jersey biotech has kept at it, starting multiple new trials in different indications.
But now the program has failed another Phase III study — definitively.
INOpulse, the company reported, did not meet the primary endpoint in a trial with 145 patients with fibrotic interstitial lung disease. Going to the secondary endpoints, Bellerophon found “minimal difference” between the treatment and placebo group, “with none approaching statistical significance.”
Unlock this article instantly by becoming a free subscriber.
You’ll get access to free articles each month, plus you can customize what newsletters get delivered to your inbox each week, including breaking news.