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猪流行性腹泻病毒mRNA疫苗(RPS1903)
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世卫组织警示基孔肯雅热疫情风险;华熙生物发布《关于网络不实信息的严正声明》丨医药早参
Mei Ri Jing Ji Xin Wen· 2025-07-27 23:19
Group 1 - The World Health Organization warns that the Chikungunya virus is spreading globally, with 119 countries reporting cases and approximately 5.5 million people at risk of infection [1] - In Foshan, Guangdong Province, over 4,000 confirmed cases of Chikungunya have been reported, with Shunde District accounting for 3,627 cases, all of which are mild [1] Group 2 - Domestic animal health mRNA vaccines are entering a clinical boom, with recent approvals for clinical trials of mRNA vaccines for pig diarrhea and cat infectious peritonitis [2] - The rapid approval of mRNA vaccines reflects an accelerating trend in the application of mRNA technology in animal health, although the high development barriers pose risks for investors [2] Group 3 - Huaxi Bio issued a statement addressing false information circulating online, emphasizing the malicious nature of the claims and the background of the individual responsible for the misinformation [3] - The company's swift response highlights its commitment to managing reputation risks, especially in the sensitive beauty and medical aesthetics industry [3] Group 4 - Guangsheng Tang announced the successful enrollment of the first subject in the Phase III clinical trial for its innovative hepatitis B treatment, GST-HG141, marking a significant milestone in its development [4] - GST-HG141 is a novel hepatitis B core protein/capsid regulator and is the first of its kind with global intellectual property rights held by Guangsheng Tang [4]
重磅消息!瑞普生物获得国内首个经济动物用mRNA疫苗临床批件【附动物疫苗行业市场分析】
Qian Zhan Wang· 2025-07-27 04:00
Core Viewpoint - Tianjin Reap Bio-Tech Co., Ltd. has received clinical trial approval for its mRNA vaccine for porcine epidemic diarrhea virus (RPS1903), marking a significant advancement in the domestic animal vaccine sector [2] Company Summary - The mRNA vaccine is the first of its kind for economic animals in China, indicating that the company has developed a mature veterinary mRNA vaccine research platform, which will help expand its product line and development space [2] - The vaccine demonstrates a 98.7% success rate in immunization during preclinical trials, significantly outperforming traditional vaccines, which have an 85.3% success rate [3] - The mRNA vaccine utilizes advanced delivery technology and can potentially encode multiple pathogen antigens, laying the groundwork for the development of multivalent vaccines [3] Industry Summary - The animal vaccine market in China reached a size of $2.5 billion in 2022, remaining stable compared to 2021, but saw a slight decline to $2.373 billion in 2023, indicating a structural upgrade trend in the industry [3] - The market is expected to exceed $3.8 billion by 2029, with a compound annual growth rate (CAGR) of 6.8%, driven by the commercialization of African swine fever vaccines and increased penetration of pet vaccines [5] - The development of new vaccine technologies, such as mRNA and genetically engineered vaccines, is providing more efficient and safer solutions for animal disease prevention and control [3]
瑞普生物:获得国内首个经济动物用mRNA疫苗临床批件
news flash· 2025-07-25 07:47
Core Viewpoint - The company has received the first clinical trial approval for an mRNA vaccine for economic animals in China, marking a significant milestone in its veterinary mRNA vaccine development platform [1] Group 1: Company Developments - The company, 瑞普生物, announced that it has obtained a clinical trial approval from the Ministry of Agriculture and Rural Affairs for its mRNA vaccine targeting porcine epidemic diarrhea virus (RPS1903) [1] - This approval signifies that the company possesses a mature research and development platform for veterinary mRNA vaccines, which is expected to broaden its product line and development opportunities [1] Group 2: Industry Context - The approval of the mRNA vaccine is a pioneering step in the domestic market for economic animals, indicating a potential shift in veterinary vaccine development [1] - It is important to note that after obtaining clinical trial approval, the vaccine must complete clinical trials and submit for registration, which involves review and approval by the Ministry of Agriculture and Rural Affairs before it can be marketed [1]