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Spero Therapeutics Jumps as Oral Carbapenem Hits Phase 3 Milestone
Spero Therapeutics Jumps as Oral Carbapenem Hits Phase 3 Milestone

Yahoo

time4 days ago

  • Business
  • Yahoo

Spero Therapeutics Jumps as Oral Carbapenem Hits Phase 3 Milestone

Spero Therapeutics, Inc. (NASDAQ:SPRO) saw its stock surge by 240% on May 28 following the company's announcement of the successful completion of the pivotal Phase 3 PIVOT-PO trial for tebipenem HBr, an investigational oral antibiotic intended for use in treating complicated urinary tract infections. The Phase 3 study, conducted in collaboration with development partner GSK plc, effectively achieved its primary goal, proving that tebipenem HBr is not inferior to the intravenous antibiotic imipenem-cilastatin in treating adult hospitalized patients with cUTI. According to a press statement issued by Spero on May 28, tebipenem HBr may be the first oral carbapenem antibiotic that patients in the U.S. can get, potentially addressing an estimated 2.9 million annual cases of cUTIs. The full trial results will be submitted to a peer-reviewed journal for publication and presentation at a later scientific convention, with Spero and GSK intending to submit the findings to the FDA in the second half of 2025. While we acknowledge the potential of SPRO to grow, our conviction lies in the belief that some AI stocks hold greater promise for delivering higher returns and have limited downside risk. If you are looking for an AI stock that is more promising than SPRO and that has 100x upside potential, check out our report about the cheapest AI stock. Read More: and . Disclosure: None. Error in retrieving data Sign in to access your portfolio Error in retrieving data Error in retrieving data Error in retrieving data Error in retrieving data

Biotech Finds Mid-Week Success After Meeting Primary Endpoint
Biotech Finds Mid-Week Success After Meeting Primary Endpoint

Globe and Mail

time5 days ago

  • Business
  • Globe and Mail

Biotech Finds Mid-Week Success After Meeting Primary Endpoint

A biotech company based out of Massachusetts found a tremendous amount of success mid-week after the company announced that the pivotal Phase 3 PIVOT-PO trial evaluating tebipenem HBr, an investigational oral treatment for complicated urinary tract infections (cUTIs), met its primary end point and will stop early for efficacy, according to a recent press release. Traders wasted no time snatching up shares of Spero Therapeutics Inc. (Nasdaq:SPRO), pushing the small cap to close the session up at $2.35/share (+244.57%). This move was a massive breakout from the multi-month downtrend this stock was stuck in since last year. Spero Therapeutics Inc is a clinical-stage biopharmaceutical firm. It focuses on identifying, developing and commercializing novel treatments for MDR (Multi-drug-resistant) bacterial infections and rare diseases. The company's product candidate, tebipenem pivoxil hydrobromide or tebipenem HBr, is designed to be an oral carbapenem-class antibiotic for use in adults to treat MDR Gram-negative infections. It is also developing SPR720, a novel oral antibiotic designed for the treatment of a rare, orphan disease caused by pulmonary non-tuberculous mycobacterial infections, or NTM disease. Besides, it is also focused on SPR206, a next-generation polymyxin investigational product candidate, being developed as an IV-administered medicine to treat MDR Gram-negative infections in the hospital. Copyright © 2025 All rights reserved. Republication or redistribution of content is expressly prohibited without the prior written consent of shall not be liable for any errors or delays in the content, or for any actions taken in reliance thereon. View more of this article on About Media, Inc.: Founded in 1999, is one of North America's leading platforms for micro-cap insights. Catering to both Canadian and U.S. markets, we provide a wealth of resources and expert content designed for everyone—from beginner investors to seasoned traders. is rapidly gaining recognition as a leading authority in the micro-cap space, with our insightful content prominently featured across numerous top-tier financial platforms, reaching a broad audience of investors and industry professionals. Want to showcase your company's story to a powerful network of investors? We can help you elevate your message and make a lasting impact. Contact us today. Contact: Media, Inc.

GSK, Spero Stop UTI Drug Trial After Early Success
GSK, Spero Stop UTI Drug Trial After Early Success

Medscape

time5 days ago

  • Business
  • Medscape

GSK, Spero Stop UTI Drug Trial After Early Success

(Reuters) -Spero Therapeutics and partner GSK are stopping a late-stage trial of an experimental oral drug for complicated urinary tract infections early as the study met its main goal, the companies said on Wednesday. Shares of Spero more than tripled to $2.24 in premarket trading. The decision comes after a recommendation from an independent committee that completed an interim analysis of data from 1,690 patients enrolled in the trial. The companies were studying the oral drug, tebipenem HBr, as a treatment for complicated urinary tract infections (cUTIs), including a type of kidney infection called pyelonephritis. An estimated 2.9 million cases of cUTIs are treated annually in the U.S. alone. The current standard of care includes antibiotics called carbapenem, but those are only available for intravenous administration. In the trial, the drug showed it was at least as good as an intravenous imipenem-cilastatin, a type of antibiotic, in hospitalized adult patients. If approved, the drug could be the first oral carbapenem antibiotic for patients with cUTIs. The review by the committee did not identify any new safety concerns beyond what had been reported in other studies, with diarrhea and headache as the two most reported side effects. The companies had entered into a licensing agreement for the development of tebipenem HBr in 2022. The U.S. FDA had previously declined to approve the drug saying a late-stage study testing it was insufficient and an additional study would be required. The British drugmaker plans to work with U.S. regulatory authorities to include the data as part of a filing in the second half of the year. Full results will be submitted for presentation at an upcoming scientific congress and for publication in a peer-reviewed journal, the companies said. (Reporting by Sriparna Roy and Yadarisa Shabong in Bengaluru; Editing by Devika Syamnath)

GSK Stops Antibiotic Trial Early After Seeing Positive Results
GSK Stops Antibiotic Trial Early After Seeing Positive Results

Bloomberg

time6 days ago

  • Business
  • Bloomberg

GSK Stops Antibiotic Trial Early After Seeing Positive Results

GSK Plc halted a trial following positive results for an oral antibiotic to treat complicated urinary tract infections that could replace an intravenous medicine that is typically used. The antibiotic called tebipenem HBr, which is being developed by GSK and Spero Therapeutics, worked as well as an intravenous antibiotic in the late stage trial, the company said Wednesday. GSK plans to file for US approval later this year and will submit the full results to an upcoming scientific congress.

GSK, Spero to stop urinary tract infection drug trial due to early success
GSK, Spero to stop urinary tract infection drug trial due to early success

Reuters

time6 days ago

  • Business
  • Reuters

GSK, Spero to stop urinary tract infection drug trial due to early success

May 28 (Reuters) - Spero Therapeutics (SPRO.O), opens new tab and partner GSK (GSK.L), opens new tab said on Wednesday an experimental drug for complicated urinary tract infections met the main goal of a late-stage trial and the companies will be stopping the trial early for efficacy. Spero shares nearly tripled to $2 in premarket trading. The decision comes after a recommendation from an independent committee that completed a pre-specified interim analysis of data from 1,690 patients enrolled in the trial. The companies were studying the oral drug, tebipenem HBr, as a treatment for complicated urinary tract infections, including pyelonephritis, in which kidneys become infected. In the trial, the drug showed it was at least as good as an existing intravenous treatment in hospitalized adult patients. GSK plans to work with U.S. regulatory authorities to include the data as part of a filing in the second half of the year.

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