Follow along with the video below to see how to install our site as a web app on your home screen.
Note: This feature may not be available in some browsers.
IP addresses are NOT logged in this forum so there's no point asking. Please note that this forum is full of homophobes, racists, lunatics, schizophrenics & absolute nut jobs with a smattering of geniuses, Chinese chauvinists, Moderate Muslims and last but not least a couple of "know-it-alls" constantly sprouting their dubious wisdom. If you believe that content generated by unsavory characters might cause you offense PLEASE LEAVE NOW! Sammyboy Admin and Staff are not responsible for your hurt feelings should you choose to read any of the content here. The OTHER forum is HERE so please stop asking.
Shares of Iterum Therapeutics(NASDAQ:ITRM) had crashed 35.5% as of 11:08 a.m. EDT on Friday. The big decline came after the company announced after the market close on Thursday that it had received a letter from the Food and Drug Administration (FDA). This letter, the company said, "identified deficiencies that preclude the continuation of the discussion of labeling and post marketing requirements/commitments at this time" for its antibiotic candidate sulopenem etzadroxil/probenecid in treating uncomplicated urinary tract infections.
Iterum had hoped to win FDA approval for sulopenem etzadroxil/probenecid this month. The agency previously assigned a Prescription Drug User Fee Act (PDUFA) date of July 25 for the completion of its review of the company's regulatory filing for the antibiotic.
The FDA's letter didn't "reflect a final decision on the information under review," according to Iterum. But it seems a foregone conclusion that any potential approval for sulopenem etzadroxil/probenecid will be later than expected.
In May, Iterum met with the FDA, and the agency shared some issues that were still under review at that time. The company said that it had responded to those issues, and that the FDA decided not to convene an advisory committee meeting to review the application for approval of sulopenem etzadroxil/probenecid.
Now what
Iterum now plans to work with the FDA to learn more about the deficiencies mentioned in the agency's letter. CEO Corey Fishman said that his company will "resolve the issues as expeditiously as possible in order to continue advancing this much needed antibiotic."