On September 4th, Huashen Technology announced its intention to relist the 51% stake in its controlling subsidiary, Tibet Kangyu Pharmaceutical Co., Ltd., for a price of 42.5 million yuan. The company had already publicly listed the shares on the Southwest United Equity Exchange, but after the second round of listing announcements expired without a qualified prospective transferee, the company decided to relist the shares. Comment: The failure to attract qualified potential transferees in the first two rounds of listing may mean that the market’s valuation expectations for the equity sale are different from the company’s, or that potential buyers have concerns about Kangyu Pharmaceutical’s future development, industry competition situation, financial status, etc. The effect of re-listing will depend on the final transfer situation and market reaction. https://finance.eastmoney.com/a/202509053505290366.html
On September 3, the marketing application for Madeuroxavir Granules, developed jointly by Simcere Pharmaceuticals and Antikang Biopharmaceuticals, was accepted for use in the treatment of uncomplicated influenza A and B in children aged 2 to 11 years. This is the first innovative anti -influenza virus drug for pediatric patients in China to successfully complete Phase III clinical trials and be approved for marketing.. Comment: If approved, the first domestically produced pediatric anti-influenza drug will create a new growth point for Simcere Pharmaceuticals and enhance its competitiveness in the anti-influenza market. It also demonstrates Antikang Biopharmaceuticals’ strength in innovative drug research and development, helping to boost its valuation in the capital market. https://finance.eastmoney.com/a/202509053505290366.html
On September 4, Lianhuan Pharmaceutical announced that its subsidiary, Xinxiang Changle Pharmaceutical Co., Ltd., had received approval in China for its amlodipine besylate tablets. Amlodipine besylate tablets are a commonly used medication for regulating vascular pressure. In 2024, sales of amlodipine besylate tablets (2.5mg/5mg/10mg) in hospitals nationwide reached 1.216 billion yuan. Comment: This event further enriches the product lines of the company and its subsidiaries, helping to enhance the market competitiveness of their products. However, this market is already crowded with numerous participants and fiercely competitive. The company needs to strengthen its marketing and channel development efforts to effectively increase its market share. https://finance.eastmoney.com/a/202509053505290366.html
Daiichi Sankyo and AstraZeneca’s TROP2-targeting antibody-drug conjugate (ADC), Dazhuoyou (generic name: dedaburumab for injection), has been approved by the China National Medical Products Administration for the treatment of adult patients with unresectable or metastatic hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative breast cancer who have previously received endocrine therapy and at least one line of chemotherapy in the advanced stage of the disease. Dazhuoyou is an Xd antibody-drug conjugate (ADC) targeting TROP2 developed using unique technology. It was developed by Daiichi Sankyo and co-developed with AstraZeneca. This is also the second DXd ADC designed using Daiichi Sankyo’s DXd ADC technology and approved in China. Breast cancer ranks second among malignant tumors in women in my country. In 2022, there were approximately 357,000 new cases of breast cancer in China, with approximately 75,000 deaths, posing a serious threat to women’s health. Approximately 70% of confirmed cases were HR-positive, ...
On September 3, Sanofiannounced that its Tilizumab Injection (trade name: Terico) has been approved by the China National Medical Products Administration (NMPA) for use in children aged 8 years and above and adults with stage 2 type 1 diabetes to delay progression to stage 3 type 1 diabetes. https://finance.eastmoney.com/a/202509033503446424.html
On September 3, 2025, Argo Biopharma Co., Ltd. announced a new strategic collaboration agreement with Novartis (NYSE: NVS) to jointly develop multiple cardiovascular products. This new agreement expands upon the existing collaboration between the two parties. Under this agreement, Argo Biopharma granted Novartis an option for ex-China rights to two early-stage molecules for the treatment of severe hypertriglyceridemia (sHTG) and mixed dyslipidemia, as well as a right of first negotiation for BW-00112 (ANGPTL3). This product is currently in Phase II clinical trials in the United States and China, with Argo Biopharma leading the subsequent combination therapy clinical trials. For another preclinical siRNA drug candidate, Argo Biopharma granted Novartis an exclusive ex-China license, including a reciprocal option to share profits and losses (P&L) in the United States and China. This product is expected to initiate Phase I clinical trials in 2026. https://finance.eastmoney.com/a/202509053505318712.html
September 4th that Dalirexant (trade name: Covitra), a global next-generation insomnia drug introduced by Simcere Pharmaceuticals, officially launched on Alibaba Health . Currently, Dalirexant is the only DORA (dual orexin receptor antagonist)-class insomnia drug approved by the European Medicines Agency to improve daytime function. Originating in Switzerland, it was jointly developed and introduced by Simcere Pharmaceuticals and Idorsia. The drug has previously been approved for marketing in 11 countries, including the United States, the United Kingdom, Switzerland, Japan, Canada, and Hong Kong. (21st Century Business Herald) https://finance.eastmoney.com/a/202509043505017121.html
September 5, Hengrui Medicine announced in the morning that it had reached an agreement with BraveheartBio, Inc. (hereinafter referred to as “Braveheart Bio”) of the United States to have independent intellectual property rights .Category 1 innovative drugsHengrui is licensed the HRS-1893 (HRS-1893) program to Braveheart Bio for a fee. Braveheart Bio will pay Hengrui an upfront payment of US$65 million (consisting of US$32.5 million in cash and an equivalent of US$32.5 million in Braveheart Bio equity) and US$10 million in near-term milestone payments upon completion of technology transfer, for a total of US$75 million. Hengrui is eligible to receive milestone payments related to clinical development and sales, up to US$1.013 billion. https://finance.eastmoney.com/a/202509053505416531.html
On the afternoon of September 5th, Hong Kong stocks opened higher and continued to rise, with innovative drugs leading the way in gains. The Hong Kong pharmaceutical ETF (159718. SZ) now rose 2.14%, with a year-on-year increase of over 89%. Component stocks such as San Sheng Pharmaceutical (01530) rose 12.00%, Kangnuoyo-B (02162) rose 10.44%, Jingtai Holdings (02228) rose 7.25%, and stocks such as Huang Pharmaceutical (00013) and Tongyuan Kangzheng-B (02410) followed suit. On the news front, the 2025 World Congress on Lung Cancer (WCLC) will be held in Barcelona, Spain from September 6th to 9th. Several innovative drug leaders will release heavyweight new products during the conference. The release and exchange of research results at academic conferences will bring new development opportunities and market attention to innovative drug companies. Institutions are optimistic about the potential for valuation recovery in the innovative drug sector, and the logic is that in the ...
Over the past few decades, the biopharmaceutical industry has been constantly advancing. From initially relying on traditional mass production processes to now exploring more intelligent and efficient continuous flow processes, the entire industry is undergoing a profound transformation. This transformation is not only expected to improve the efficiency and quality of drug supply, but also directly related to the accessibility of patient medication and the sustainable development of the healthcare system. For the general public, these seemingly professional terms are actually closely related to our daily health. Recently, the life science group Sartorius teamed up with the Shanghai Biopharmaceutical Industry Association to hold the 2025 Enhanced Process Summit. The summit gathered industry experts, scholars, and business representatives from around the world, focusing on the cutting-edge trends and development paths of biopharmaceutical continuous flow strengthening processes, and re emphasizing the release of the “White Paper on Biopharmaceutical Continuous Flow Strengthening Processes”. ...
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