- Iterum Therapeutics plc ITRM has concluded a late-cycle meeting with the FDA related to its application for sulopenem etzadroxil/probenecid.
- Sulopenem is under review as a treatment for uncomplicated urinary tract infections in patients with a quinolone non-susceptible pathogen.
- The agency determined that an Advisory Committee meeting is not currently necessary and is continuously working toward the action date of July 25.
- During the meeting, the FDA shared issues still under review, and the company responded.
- In April, the company disclosed that the FDA needed additional time to review its sulopenem application, and FDA Antimicrobial Drugs Advisory Committee June 2 meeting has been postponed.
- Price Action: ITRM shares are up 22.8% at $1.51 during the premarket session on the last check Friday.
- Related content: Benzinga's Full FDA Calendar
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