Spero Therapeutics Announces Early Success in Phase 3 Trial of Tebipenem HBr for Complicated UTIs, Plans FDA Filing in 2025

Reuters
05-28
Spero <a href="https://laohu8.com/S/LENZ">Therapeutics</a> Announces Early Success in Phase 3 Trial of Tebipenem HBr for Complicated UTIs, Plans FDA Filing in 2025

CAMBRIDGE, Mass., May 28, 2025 - Spero Therapeutics Inc. and GSK plc have announced the early conclusion of their pivotal Phase 3 PIVOT-PO trial for tebipenem HBr, an investigational oral treatment for complicated urinary tract infections (cUTIs), including pyelonephritis. The trial ended early following a recommendation from an Independent Data Monitoring Committee, which found that the primary endpoint of non-inferiority compared to intravenous imipenem-cilastatin had been met. The trial involved 1,690 patients and did not reveal any new safety concerns. If approved, tebipenem HBr could become the first oral carbapenem antibiotic available for U.S. patients with cUTIs. Data from the trial will be included in a planned FDA filing in the second half of 2025.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Spero Therapeutics Inc. published the original content used to generate this news brief via EDGAR, the Electronic Data Gathering, Analysis, and Retrieval system operated by the U.S. Securities and Exchange Commission (Ref. ID: 0001193125-25-128680), on May 28, 2025, and is solely responsible for the information contained therein.

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