BRIEF-Eylea Hd® (Aflibercept) Injection 8 Mg Sbla Accepted For FDA Priority Review

Reuters

2025/04/17

April 17 (Reuters) - Regeneron Pharmaceuticals Inc REGN.O:

EYLEA HD® (AFLIBERCEPT) INJECTION 8 MG SBLA ACCEPTED FOR FDA PRIORITY REVIEW FOR BOTH THE TREATMENT OF MACULAR EDEMA FOLLOWING RETINAL VEIN OCCLUSION (RVO) AND FOR MONTHLY DOSING IN APPROVED INDICATIONS
REGENERON PHARMACEUTICALS INC - FDA TARGET ACTION DATE FOR EYLEA HD SBLA IS AUGUST 19, 2025

Source text: ID:nGNX9kVwHX

Further company coverage: REGN.O

((Reuters.Briefs@thomsonreuters.com;))

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</span>Regeneron Pharmaceuticals Inc <span>REGN.O</span>:</p><ul><li><p>EYLEA HD® (AFLIBERCEPT) INJECTION 8 MG SBLA ACCEPTED FOR FDA PRIORITY REVIEW FOR BOTH THE TREATMENT OF MACULAR EDEMA FOLLOWING RETINAL VEIN OCCLUSION (RVO) AND FOR MONTHLY DOSING IN APPROVED INDICATIONS</p></li><li><p>REGENERON PHARMACEUTICALS INC - FDA TARGET ACTION DATE FOR EYLEA HD SBLA IS AUGUST 19, 2025</p></li></ul><p>Source text: <span>ID:nGNX9kVwHX</span></p><p>Further company coverage: <span>REGN.O</span></p><p> ((Reuters.Briefs@thomsonreuters.com;))</p></body></html>\n\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":"LU0289739699.SGD","symbol_name":"AB INTERNATIONAL HEALTH CARE PORTFOLIO \"A\" (SGD) ACC","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20250417:nTUA9QTTVX:1","article_id":"2528790149","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2528790149","pubTimestamp":1744888023,"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":"BRIEF-Eylea Hd (Aflibercept) Injection 8 Mg Sbla Accepted For FDA Priority Review April 17 (Reuters) - 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Regeneron Pharmaceuticals Inc REGN.O:EYLEA HD® (AFLIBERCEPT) INJECTION 8 MG SBLA ACCEPTED FOR FDA PRIORITY REVIEW FOR BOTH THE TREATMENT OF MACULAR EDEMA FOLLOWING RETINAL VEIN OCCLUSION (RVO) AND FOR MONTHLY DOSING IN APPROVED INDICATIONSREGENERON PHARMACEUTICALS INC - FDA TARGET ACTION DATE FOR EYLEA HD SBLA IS AUGUST 19, 2025Source text: ID:nGNX9kVwHXFurther company coverage: REGN.O ((Reuters.Briefs@thomsonreuters.com;))","kind":"highlight","is_publish_news":true,"is_publish_highlight":false,"is_publish_live":false,"is_publish_wemedia":null,"editions":null,"column":"","sentiment":"1","news_tag":"","news_rank":0,"symbols":[],"gpt_button":1,"need_auth":false,"code":"91000000","status":"200"}}}