AIM Vaccine Gets Marketing Approval from China's NMPA After Phase III Trials Completion

MT Newswires Live

2024/11/01

AIM Vaccine (HKG:6660) said it applied for marketing registration for its 13-valent pneumonia conjugate vaccine with the National Medical Products Administration (NMPA) after its phase-III clinical trials were completed, according to a Friday filing with the Hong Kong bourse.

The results of the Phase III clinical trials were completed unblinding. The vaccine has good immunogenicity and safety and met the pre-defined clinical objectives, the filing added.

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The vaccine has good immunogenicity and safety and met the pre-defined clinical objectives, the filing added.</p></body></html>\n\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":"BK1161","symbol_name":"生物科技","start_time":0,"source_url":"https://www.mtnewswires.com/","article_id":"2480074110","we_media_id":"1092851196","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2480074110","pubTimestamp":1730453233,"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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