1. Jimu Biological License: Tian Tian Pharmaceutical ARVN001 600 million yuan On November 13th, Tian Shan Pharmaceutical and Ji Mu Biotechnology announced that Ji Mu Biotechnology has authorized Tian Shan Pharmaceutical with exclusive commercial rights for its ARVN001 (Triamcinolone Acetonide Choroidal Injection Suspension) under development in mainland China. ARVN001 uses a suprachoroidal microinjection (SCS microinjection) system ®) The patented technology will be used to treat uveitis related macular edema (UME) and other potential ophthalmic indications under development. Jimu Biotech will receive a total down payment and milestone payments of up to 85 million US dollars (approximately 600 million RMB). Previously, Jimu Biotechnology obtained the rights to develop and commercialize this therapy in the Asia Pacific region from Clearside Biomedical Inc. In July 2024, Jimu Biotechnology announced that ARVN001 achieved positive top line results in the Phase III clinical trial of UME in China. Meanwhile, research on the use of this ...
On November 20, local time, Jazz Pharmaceuticals announced that the U.S. FDA has accelerated the approval of its HER2-targeted bispecific antibody Zanidatamab (Ziihera), developed in collaboration with Zymeworks, for marketing for the treatment of patients with previously treated, unresectable, locally advanced or metastatic HER2-positive biliary tract cancer. The press release pointed out that this is the first and only HER2 bispecific antibody approved by the FDA for HER2+ biliary tract cancer. Zanidatamab (ZW25) is a bispecific antibody based on the Zymeworks Azymetric platform that can simultaneously bind to two non-overlapping HER2 epitopes, i.e., biparatopic binding. This unique design can form multiple mechanisms of action, including dual blocking of HER2 signals, enhanced binding and removal of HER2 proteins on the cell surface, and strong antibody effector functions to enhance anti-tumor activity in patients. Previously, Zenidatumomab has been granted breakthrough therapy designation, fast track qualification, priority review qualification, orphan drug qualification, etc. ...
On November 21, China Resources Pharmaceutical issued the “Latest Information on the Proposed Internal Restructuring of its China Resources Shenghuo” announcement. China Resources Sanjiu and Kunming Pharmaceutical Group have entered into an equity transfer agreement. China Resources Sanjiu has conditionally agreed to sell, and Kunming Pharmaceutical Group has conditionally agreed to acquire 51% of the equity of China Resources Shenghuo, with a total price of 1.791 billion yuan (equivalent to approximately HK$1.938 billion). It is expected that China Resources Sanjiu will use the funds to supplement operating funds. After the internal restructuring is completed, China Resources Pharmaceutical’s interest in China Resources Shenghuo will be reduced from approximately 63.02% to 39.90%, and China Resources Shenghuo will remain a non-wholly owned subsidiary of China Resources Pharmaceutical. On the same day, China Resources Sanjiu announced that it had signed the “Equity Transfer Agreement between China Resources Sanjiu Pharmaceutical Co., Ltd. and Kunming Pharmaceutical ...
On November 15, according to the official website of CDE, the Class 1 new drug DR10624 injection of Huadong Medicine’s subsidiary Daoer Biotechnology has obtained implicit approval for clinical trials, and its indications are metabolic-related fatty liver disease/metabolic-related fatty hepatitis. According to public information, the drug is a GLP-1R/GCGR/FGF21R triple agonist. DR10624 is a chimeric peptide segment targeting GLP1R/GCGR at the N-terminus, fused to an engineered IgG1 Fc, and a recombinant FGF21 mutant is fused to the C-terminus of the Fc. Preclinical study results show that DR10624 has strong metabolic regulation and improved efficacy. Huadong Medicine mentioned in the announcement that DR10624 is a symmetrical dimer in structure. While having the biological activity of GLP-1R, GCGR, and FGF21R triple agonists, it can also be fused with a deglycosylated IgG1 Fc to extend the half-life. In April 2022, Doer Biopharma was approved to conduct a Phase I clinical trial of DR10624 ...
AtriCure, a leading company in the treatment of atrial fibrillation, announced today that its EnCompass cardiac tissue ablation clip has received the EU CE mark, meaning the device can be sold in more than 30 countries in the European Economic Area (EEA). A number of innovative products were launched AtriCure was founded in 2000 and focuses on cardiac surgery solutions. The company mainly produces and sells cardiac ablation devices, providing innovative technologies for the treatment of atrial fibrillation and related diseases. At present, AtriCure has 138 authorized patents in the United States and has served more than 300,000 patients with atrial fibrillation since 2004. It is understood that the EnCompass cardiac tissue ablation clamp is used for cardiac tissue ablation surgery, including comprehensive epicardial ablation of the left atrium during open heart surgery. This is a simpler and faster method of open-chest cardiac ablation, allowing doctors to perform comprehensive epicardial ...
Organiser:Informa Markets Time:May 20th – 23rd, 2025 Address: Centro de Exposições Imigrantes, Rodovia dos Imigrantes, Km 1.5, São Paulo – SP Exhibition hall:São Paulo Expo Product range: Medical Equipment Exhibition Area: Hospital technology facilities and equipment; medical clinic technology and equipment; ward furniture and equipment; diagnostic and treatment equipment; biochemical and testing equipment; pharmaceutical products; hygienic materials; medical communication technology and equipment; comprehensive hospital information technology and services. Rehabilitation Technology for Disabled Exhibition Area: Nursing equipment; nursing products; communication technology; mobile nursing; nursing services; medical technology; orthopedic technology; outpatient nursing; physiotherapy; prosthetics; services; ergotherapy; communication technology; wheelchairs. Pharmaceutical Exhibition Area: Prescription drugs; traditional Chinese medicines; western medicines; antibiotics; powdered injections; infusions; tablets; ointments; capsules; various new drugs; specialty drugs; national protected traditional Chinese medicine varieties; national basic medical insurance drugs; pharmaceutical raw materials; various intermediates; biochemical reagents and vaccines; various biological products. Dental Exhibition Area: Dental instruments and equipment; dental ...
A person in charge of Northeast Pharmaceutical recently stated in an interview with China Securities Journal that in recent years, the company has strategically laid out a new track for biopharmaceuticals and seized the pharmaceutical “blue ocean” market with more “new brand” products. In the future development, the company will continue to implement the “innovation+imitation” dual wheel drive strategy, and on the basis of further strengthening traditional businesses such as raw materials and chemical generic drugs, continue to focus on the new track of biopharmaceuticals, fully build new advantages for latecomers, and provide strong impetus for long-term development. Entering the field of cell therapy As an old pharmaceutical company with a history of 78 years, Northeast Pharmaceutical has always focused on raw materials and chemical generic drugs as its main products. It should be noted that in the pharmaceutical industry, including sub sectors such as chemical drugs, the track is ...
Drugdu.com expert’s response: In the context of normalized centralized procurement, the medical device industry faces a new market environment and competitive landscape. To explore new channels and markets, enterprises can proceed from the following aspects: Ⅰ. Optimize Resource Allocation to Enhance Product Competitiveness Focus on Innovative Research and Development: Medical device enterprises should increase investment in innovative research and development to launch products with differentiated competitive advantages, thereby avoiding the risks associated with centralized procurement of homogeneous products. Through innovation, enterprises can open up new market segments, meet the needs of specific patients, and thus obtain higher market shares and profit margins. Diversify Product Lines: Expand the industry chain and enhance risk resistance capabilities with a multi-product portfolio. Enterprises can achieve seamless integration of the industry chain by acquiring upstream and downstream related enterprises, thereby enhancing product competitiveness and creating a synergistic effect. Ⅱ. Leverage Centralized Procurement Platforms to Expand Sales ...
Together with Takeda Pharmaceuticals and Corplex, Schott Pharmaceuticals has successfully conducted a ton level emission reduction pilot study, improving resource utilization efficiency and reducing carbon emissions in the pharmaceutical supply chain Research has shown that closed-loop recycling of pallets used for packaging and shipping drug sealing solutions is technically and supply chain feasible. When using 70% recycled materials for pallets, greenhouse gas (GHG) emissions can be reduced by up to 50%. Schott Pharmaceuticals, a supplier of drug packaging and delivery solutions, Corplex, a leader in transportation packaging design, manufacturing, and recycling, and Takeda Pharmaceuticals, a leading global biopharmaceutical company, are collaborating to promote circular economy solutions in the pharmaceutical industry. Three companies have collaborated to conduct a pilot study on the closed-loop recycling of disposable pallets. During drug transportation, these trays are used to hold injection bottles, syringes, and ampoules, and are currently only for disposable use. We strive to ...
As one of the important treatment methods for tumors, the global radiotherapy industry is currently entering the path of precision, intelligence, and personalized development. Among them, precision radiotherapy, as an efficient, personalized, and precise cancer treatment method, is considered a new era in cancer treatment. Recently, there has been good news from the radiation therapy industry once again. On November 25th, Baiyang Pharmaceutical officially announced the acquisition of ZAP Surgical Systems, Inc.’s head and neck X-ray radiosurgery treatment system (trade name: ZAP-X) ® The exclusive commercial rights of the Mars Ark Radiosurgical Robot (ZAP-X) and related accessories in mainland China, Hong Kong, and Macau will fully promote the faster landing and wider application of ZAP-X in the Chinese market. 01. The world’s first self shielded radiotherapy surgical robot, solving pain points in the head and neck radiation surgery industry Public information shows that the common indications for ZAP-X include all ...
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