Verve Therapeutics Gets FDA Fast Track Designation for VERVE-102

MT Newswires Live

04/11

Verve Therapeutics (VERV) said Friday the US Food and Drug Administration granted fast track designation for its experimental VERVE-102 treatment for hyperlipidemia and high lifetime cardiovascular risk to lower low-density lipoprotein cholesterol.

The company is testing VERVE-102 in a phase 1b clinical trial. The study's demographic and initial safety and efficacy data are expected in Q2.

Verve Therapeutics shares were up 4.9% in recent premarket activity.

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The study's demographic and initial safety and efficacy data are expected in Q2.</p><p>Verve <a href=\"https://laohu8.com/S/LENZ\">Therapeutics</a> shares were up 4.9% in recent premarket activity.</p></body></html>\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":"FAST","symbol_name":"快扣","start_time":0,"source_url":"https://www.mtnewswires.com/","article_id":"2526668852","we_media_id":"1092851196","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2526668852","pubTimestamp":1744371630,"columns":[],"sourceInfo":{"source_id":"mtnewswires_news","name":"MT Newswires"},"weMediaInfo":{"media_name":"MT Newswires Live","introduction":"The most recognized names in North America, Europe and Asia rely on MT Newswires to power their applications. 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