- Iterum Therapeutics plc ITRM has agreed with the FDA under the special protocol assessment (SPA) process on the design, endpoints, and statistical analysis of a Phase 3 trial for oral sulopenem etzadroxil-probenecid for uncomplicated urinary tract infections.
- The pivotal study under the SPA agreement is designed as a non-inferiority trial comparing oral sulopenem and Augmentin (amoxicillin/clavulanate).
- Related: Iterum Expects To Start Additional Sulopenem Trial In Urinary Tract Infections In 2H22.
- Patients will be randomized to receive either oral sulopenem twice daily for five days or Augmentin twice daily for five days.
- The primary endpoint is the overall response at Day 12 of the study.
- The study is expected to enroll approximately 1,966 patients and is anticipated to start enrolling in the fourth quarter of 2022.
- The Company has already commenced study start-up activities to enable timely initiation and recruitment.
- Price Action: ITRM shares are up 62.10% at $0.39 during the market session on the last check Monday.
© 2024 Benzinga.com. Benzinga does not provide investment advice. All rights reserved.
Comments
Loading...
Benzinga simplifies the market for smarter investing
Trade confidently with insights and alerts from analyst ratings, free reports and breaking news that affects the stocks you care about.
Join Now: Free!
Already a member?Sign in