aTyr Pharma Reveals Efzofitimod Trial Failure in Investor Call

Reuters11-21

aTyr Pharma Reveals Efzofitimod Trial Failure in Investor Call

aTyr Pharma Inc.'s management held an investor call on September 15, 2025, to address the results of the EFZO-FIT study for their drug Efzofitimod. During the call, they announced that the study did not meet its primary endpoint in changing the mean daily OSC dose at week 48. The company also stated that it would engage with the FDA to determine a path forward in light of the disappointing topline results. The full podcast discussing the class action lawsuit related to these events can be accessed at https://www.podbean.com/player-v2/?i=mj5ct-19ad352-pb&from=pb6admin&pbad=0&share=1&download=1&rtl=0&fonts=Arial&skin=1&font-color=auto&logo_link=episode_page&btn-skin=7.

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. aTyr Pharma Inc. published the original content used to generate this news brief via ACCESS Newswire (Ref. ID: 1105635) on November 21, 2025, and is solely responsible for the information contained therein.

Disclaimer: Investing carries risk. This is not financial advice. The above content should not be regarded as an offer, recommendation, or solicitation on acquiring or disposing of any financial products, any associated discussions, comments, or posts by author or other users should not be considered as such either. It is solely for general information purpose only, which does not consider your own investment objectives, financial situations or needs. TTM assumes no responsibility or warranty for the accuracy and completeness of the information, investors should do their own research and may seek professional advice before investing.

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During the call, they announced that the study did not meet its primary endpoint in changing the mean daily OSC dose at week 48. The company also stated that it would engage with the FDA to determine a path forward in light of the disappointing topline results. The full podcast discussing the class action lawsuit related to these events can be accessed at https://www.podbean.com/player-v2/?i=mj5ct-19ad352-pb&from=pb6admin&pbad=0&share=1&download=1&rtl=0&fonts=Arial&skin=1&font-color=auto&logo_link=episode_page&btn-skin=7.\n      \n\nDisclaimer: 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. aTyr Pharma Inc. published the original content used to generate this news brief via ACCESS Newswire (Ref. 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