Sangamo submits ST-920 BLA clinical and preclinical modules to FDA for Fabry disease accelerated approval review

Reuters

03/09

Sangamo submits ST-920 BLA clinical and preclinical modules to FDA for Fabry disease accelerated approval review

Sangamo advanced its rolling BLA submission to the FDA seeking accelerated approval of ST-920 for adults with Fabry disease. The company said it has submitted the preclinical and clinical modules for FDA review. Sangamo also said its antibody assay companion diagnostic was submitted to and accepted by the FDA’s Center for Devices and Radiological Health for Premarket Approval.

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. Sangamo Therapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202603090805PRIMZONEFULLFEED9667691) on March 09, 2026, and is solely responsible for the information contained therein.

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The company said it has submitted the preclinical and clinical modules for FDA review. Sangamo also said its antibody assay companion diagnostic was submitted to and accepted by the FDA’s Center for Devices and Radiological Health for Premarket Approval.\n      </p>\n</div><div xmlns:xsd=\"http://www.w3.org/2001/XMLSchema\" xmlns:xsi=\"http://www.w3.org/2001/XMLSchema-instance\">\n<p>\n<i>Disclaimer: <span>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. <a href=\"https://laohu8.com/S/SGMO\">Sangamo Therapeutics Inc</a>. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202603090805PRIMZONEFULLFEED9667691) on March 09, 2026, and is solely responsible for the information contained therein.</span></i>\n</p>\n</div></body></html>\n\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":"NDAQ","symbol_name":"纳斯达克OMX交易所","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260309:nNDL10sQg7:1","article_id":"2618636625","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2618636625","pubTimestamp":1773057985,"columns":[],"sourceInfo":null,"weMediaInfo":{"media_name":"Reuters","introduction":"Reuters.com brings you the latest news from around the world, covering breaking news in markets, business, politics, entertainment and technology","home_visible":1,"id":"1032215980","head_image":"https://community-static.tradeup.com/news/4567337cbdf294b657b1fa87c5488b48"},"summary":"Sangamo advanced its rolling BLA submission to the FDA seeking accelerated approval of ST-920 for adults with Fabry disease. 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