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| Date | Press release |
|---|---|
| 2026-05-13 17:08:00 | New England Journal Of Medicine Publishes Shionogi Study Demonstrating Ensitrelvir Prevents Covid-19 Following Exposure Osaka, japan--(business wire)--shionogi & co., ltd. (head office: osaka, japan; chief executive officer: isao teshirogi, phd; hereinafter โshionogiโ) announced that results from its global, double-blind, randomized, placebo-controlled phase 3 study, scorpio-pep, were published in the new england journal of medicine. a five-day course of ensitrelvir significantly reduced the risk of symptomatic covid-19 by 67% in individuals following exposure to an infected individual through day 10 compare. |
| 2026-04-08 08:30:00 | Shionogi Receives Contract With U.s. Government Through Bardaโs Project Bioshield To Enhance National Preparedness For Drug-resistant Bacterial Threats Osaka, japan--(business wire)--shionogi & co., ltd. (head office: osaka, japan; chief executive officer: isao teshirogi, ph.d.; hereafter โshionogiโ) announced that shionogi inc., a new jersey-based subsidiary of shionogi, has been awarded a contract through the biomedical advanced research and development authorityโs (barda) project bioshield related to fetrojaยฎ (cefiderocol) as a critical countermeasure against difficult-to-treat gram-negative bacterial infections and pathogens that prese. |
| 2026-04-01 19:30:00 | Shionogi Completes Acquisition Of All Rights To Radicava (edaravone) Osaka, japan--(business wire)--shionogi & co., ltd. (head office: osaka, japan; chief executive officer: isao teshirogi, ph.d.; hereafter โshionogiโ) announced that we have completed the transfer of all rights for radicava (edaravone), including intellectual property rights and sales rights, in major countries and regions to our company from tanabe pharma corporation. transfer of rights in additional countries and regions is forthcoming. the acquisition and integration of radicava team memb. |
| 2026-03-19 08:45:00 | Shionogi Announces First Patients Enrolled In Global Phase 2 Clinical Trial In Adults With Late-onset Pompe Disease Osaka, japan--(business wire)--shionogi & co., ltd. (head office: osaka, japan; chief executive officer: isao teshirogi, ph.d.; hereafter โshionogiโ) announced the first patients were enrolled in esprit, a global phase 2 clinical trial evaluating s-606001, an investigational drug for the treatment of late-onset pompe disease (lopd). esprit is a multicenter, randomized, placebo-controlled, double-blind study evaluating the safety, pharmacodynamics and preliminary efficacy of s-606001 as an o. |
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