“With the advancement of technology, we can achieve an accuracy rate of more than 90% in peripheral blood diagnosis of Alzheimer’s disease. Now many diagnostic companies have contacted us to carry out results transformation.” Recently, Alzheimer’s disease (hereinafter referred to as AD) expert Yu Jintai revealed to Jiemian News. Yu Jintai is the deputy dean of Fudan University Institute of Science and Technology, director of the Research Department of Shanghai Medical College of Fudan University, and deputy director of the Department of Neurology of Huashan Hospital Affiliated to Fudan University. Previously, he and the team of Professor Mao Ying, dean of Huashan Hospital, jointly with the team of Professor Feng Jianfeng and Cheng Wei of Fudan Brain-like Intelligence Science and Technology Research Institute, led a study to find a new AD peripheral blood protein target. Blood draws can predict the risk of dementia 15 years in advance, with an accuracy ...
In 1982, Weinberg and other laboratories discovered HRAS in human bladder cancer cells T24/EJ, making RAS the first human tumor gene discovered. Subsequently, other tumor genes KRAS and NRAS were also discovered. However, in the following decades, no targeted drugs for the KRAS gene have been successfully developed, and KRAS is considered an “undruggable” target. In 2021, the first KRAS G12C inhibitor, Sotorasib, was launched, making KRAS a hot target in the field of oncology. However, its clinical and commercialization progress after its launch was not satisfactory. Therefore, pan-KRAS inhibitors that can target multiple mutation forms of the KRAS gene have become a new research direction in the field of KRAS targeted drugs. The close connection between KRAS gene and cancer The full name of the KRAS gene is Kirsten Rat Sarcoma Viral Oncogene Homolog, which means “Kirsten rat sarcoma viral oncogene homolog” in Chinese. It is a proto-oncogene that ...
Drugdu.com expert’s response: The Chinese-made ECMO system has obtained EU Medical Device Certification, and the characteristics of this system are mainly embodied in the following aspects: I. Independent Research and Development and Technological Innovation This ECMO system is independently developed by Shenzhen Hanno Medical Technology Co., Ltd., a Chinese enterprise, marking a significant breakthrough for China in the field of high-end medical equipment. The system adopts advanced deep learning algorithms, enhancing cardiopulmonary support for patients through precise data analysis and real-time monitoring. II. Four Core Products Extracorporeal cardiopulmonary support auxiliary equipment: Provides critical support for patients with cardiopulmonary insufficiency. Disposable membrane oxygenator set: Ensures hygiene and safety during the oxygenation process. Disposable membrane oxygenator: Achieves efficient exchange of oxygen and carbon dioxide. Disposable centrifugal pump head: Provides stable and reliable power support. III. Wide Range of Applications This system is not only suitable for cardiopulmonary support within hospitals but can ...
With the advancement of technology, we can improve the accuracy of peripheral blood diagnosis of Alzheimer’s disease to over 90%. Now, multiple diagnostic companies have contacted us to carry out achievement transformation. Recently, Alzheimer’s disease (AD) expert Yu Jintai revealed to Interface News. Yu Jintai is the Vice Dean of the Institute of Science and Technology at Fudan University, the Director of the Research Department at Fudan University Shanghai Medical College, and the Deputy Director of the Neurology Department at Fudan University Affiliated Huashan Hospital. Previously, he and the team led by Professor Mao Ying, the director of Huashan Hospital, collaborated with Professor Feng Jianfeng and Professor Cheng Wei from Fudan Institute of Brain Intelligence Science and Technology to conduct a study that identified new peripheral blood protein targets for Alzheimer’s disease. By drawing blood, the risk of dementia can be predicted 15 years in advance, with an accuracy ...
Real life submission to the main board of the Hong Kong Stock Exchange, with China International Capital Corporation as its exclusive sponsor. The prospectus shows that RealBio is a biotechnology company driven by innovative research and development, focusing on the development, manufacturing, and commercialization of innovative drugs for the treatment of viral infections, tumors, and cardiovascular and cerebrovascular diseases. Our mission is to improve human health through true innovation, especially in the fields of antiviral and anti-tumor treatments, exploring and addressing the issue of drug resistance in existing treatment options. The company aims to seek updated and better treatment options to address unmet clinical needs. With rich experience in drug development, RealBio has established a comprehensive research and development platform, including a highly selective new nucleoside broad-spectrum anti-tumor drug development platform, TOPO1 inhibitor and XDC drug development platform, drug target discovery and validation platform, and innovative drug design and optimization ...
At the beginning of the Spring Festival, DeepSeek quickly became popular, and then the topic of AI software predicting the future became a hot topic, sparking discussions among netizens. Similar topics such as “using DeepSeek to predict the future development direction of the pharmaceutical industry”, “predicting the top ten golden tracks for medical devices in 2025”, and “predicting the investment trend in the medical device industry in 2025” are constantly emerging. Is AI prediction reliable? To explore this question and continue the AI speculation, in DeepSeek’s eyes, who will be the top 10 most valuable innovative medical devices in China? Today we will pose this question to DeepSeek, using its intelligent analysis to examine the current development status of innovative medical devices in China. DeepSeek defines innovative medical devices Value evaluation criteria for innovative medical devices – According to the Special Approval Procedure for Innovative Medical Devices, selected products must ...
Today (February 18th), Zhuhai Beihai Biotechnology Co., Ltd. (referred to as “Beihai Biotechnology”) announced that it has reached a significant strategic cooperation with Zydus Lifesciences, granting its new drug BEIBRAY (docetaxel BH009) exclusive commercialization rights in the US market. The news pointed out that BEIZRA is the first improved new drug in China to successfully achieve authorization for export to the United States in recent years. According to the terms of the agreement, Beihai Biotechnology will be responsible for the production and supply of BEIBRAY, while Zydus Pharmaceuticals, a US subsidiary of Zydus, will be responsible for the commercialization of the product in the United States. Beihai Biotechnology will receive a down payment of $15 million (to be paid after the agreement is signed) and $10 million (to be paid after the first product delivery), as well as multiple sales milestone payments and high double-digit profit sharing. According to a ...
On February 17, Watson Pharmaceuticals announced that the company recently received the “Drug Re-registration Approval Notice” for the company’s product Orlistat Capsules approved and issued by the Chongqing Municipal Drug Administration. The drug approval number of Orlistat Capsules is valid until January 22, 2030. The product was originally a cooperative product of the company. At the end of 2021, the company reached a further agreement with its partners to sell and operate Orlistat Capsules under its own brand “Quchang”. At present, this variety has little impact on the company’s operating income and profits. It will not have a significant impact on the company’s operating performance in the short term. https://finance.eastmoney.com/a/202502173321214653.html
Baili Tianheng (688506) announced on the evening of February 18 that the company recently received the “Drug Clinical Trial Approval Notice” officially approved and issued by the National Medical Products Administration (NMPA), and the Phase II/III clinical trial of the company’s independently developed innovative biological drug BL-M07D1 (HER2-ADC) for injection was approved. As of the disclosure date of this announcement, in addition to the newly approved clinical trial, BL-M07D1 is being evaluated as a single drug or in combination in 10 Phase I/II/III clinical trials in China and the United States. The various clinical studies include patients with various HER2-expressing/mutated solid tumors (including non-small cell lung cancer, breast cancer, urothelial carcinoma, gynecological tumors and digestive tract tumors). https://finance.eastmoney.com/a/202502183322435142.html
Reporters learned from Merck that Beijing’s male HPV vaccination work has been fully launched. Related studies have confirmed that HPV vaccines can provide lasting protection and are safe. Several new indications of the quadrivalent human papillomavirus vaccine (brewer’s yeast) have been approved for marketing by the National Medical Products Administration and are suitable for males aged 9-26. This is the first and currently the only HPV vaccine approved for males in China, filling an important gap in the field of male HPV prevention. Merck said that at present, the supply of vaccines in Beijing is stable, and the official platform for male HPV vaccination appointments has been officially opened. Citizens only need to pull down the Jingtong applet on WeChat, find vaccination in the “appointment registration” on the main page, enter to make a vaccine appointment, or download the Capital Vaccine Service app to make the same appointment, and then ...
Go to Page Go
your submission has already been received.
OK
Please enter a valid Email address!
Submit
The most relevant industry news & insight will be sent to you every two weeks.