According to a new research published in the journal Cell Reporting Medicine on the 10th, the team of the University of Massachusetts Amherst in the United States has developed a nano vaccine to prevent animal cancer, which has shown significant effects in preventing mouse melanoma, pancreatic cancer and triple negative breast cancer. Among the mice vaccinated with this vaccine, up to 88% remained tumor free (the specific proportion varies depending on the type of cancer), and the vaccine effectively inhibited the spread of cancer cells, even completely preventing metastasis in some cases. This platform technology has broad applicability and can be used for the prevention and treatment of various types of cancer, and is expected to be used in high-risk cancer populations in the future. Previous team research has demonstrated that this nanoparticle based drug design can shrink and eliminate tumors in mice. This study further confirms that the ...
Recently, Nuocheng Jianhua and global biopharmaceutical company Zenas jointly announced a global authorization cooperation agreement, with a potential total transaction amount of over 2 billion US dollars, adding another heavyweight footnote to China’s innovative drugs going global. Since 2025, the trend of innovative drugs going global has continued to heat up. Previously, leading pharmaceutical companies such as Hengrui Pharmaceutical and Xinda Biotechnology have successively achieved international breakthroughs in technology and market through overseas authorization. Analysts believe that the continuous increase in the amount and quantity of foreign authorizations for innovative drugs in China is an inevitable trend after the research and development capabilities in this field are globally recognized. In the past few years, the product data of domestic innovative pharmaceutical companies has continuously verified their clinical value, from early individual enterprise breakthroughs to collective global cooperation today. Essentially, it is the global market’s recognition of Chinese pharmaceutical companies’ “efficient ...
FDA announced its approval of Boehringer Ingelheim’s Jascayd (nerandomilast) tablets for the treatment of idiopathic pulmonary fibrosis (IPF). Jascayd’s approval makes it the first approved new therapy treatment for IPF in over 10 years, and with IPF being a rare, serious, and progressive disease with no cure and limited treatments, the approval marks a significant step in supporting those suffering from the disease. FDA’s approval of Jascayd was a data backed decision FDA based its approval on results collected from two Phase III trials, Fibroneer-IPF and Fibroneer-ILD.1 Jascayd’s efficiency was evaluated in both randomized, double-blind, placebo-controlled trials of adults with IPF.1 The primary endpoint was the absolute change from baseline in Forced Vital Capacity, which is the maximum amount of air a person can forcefully exhale after taking the deepest possible breath.1 Results indicated that Participants administered with Jascayd had significantly reduced FVC decline when compared to participants treated with ...
By Dennis Thompson HealthDay ReporterTHURSDAY, Oct. 9, 2025 (HealthDay News) — A widely prescribed opioid painkiller is not all it’s cracked up to be, a new evidence review has concluded. The opioid painkiller tramadol does little to reduce moderate to severe pain, according to results published Oct. 7 in the journal BMJ Evidence Based Medicine. At the same time, tramadol increases a person’s risk of serious side effects, including heart disease and pre-cancerous cells, researchers found. The drug’s use should be minimized, and guidelines that recommend it reconsidered, the research team concluded. “The potential harms associated with tramadol use for pain management likely outweigh its limited benefits,” wrote the research team led by Jehad Ahmad Barakji of the Center for Clinical Intervention Research at Rigshospitalet in Copenhagen, Denmark. Tramadol is a dual-action opioid, researchers said in background notes. It works on the usual opioid receptors in the brain, much like ...
PlasmidFactory GmbH and the Fraunhofer Institute for Cell Therapy and Immunology IZI have signed a Memorandum of Understanding to combine expertise in cell therapy process development and GMP manufacturing, aiming to accelerate non-viral cell and gene therapies for the benefit of patients. PlasmidFactory GmbH, a leading European CDMO for plasmid and Minicircle DNA, brings more than 25 years of experience and over 3,500 DNA constructs delivered worldwide. The Fraunhofer IZI contributes extensive translational capabilities in immuno-oncology, regenerative medicine, and advanced cell manufacturing. Together, they are accelerating the development of next-generation, virus-free genetic engineering platforms while maintaining the highest quality and regulatory standards. In the past, the two partners have already successfully established new manufacturing processes for CAR-T cells at Fraunhofer IZI and conducted joint research projects on virus-free gene transfer, which served as the foundation for the production of clinical cell products. By building on our long-standing collaboration, this partnership ...
By Dennis Thompson HealthDay ReporterWEDNESDAY, Oct. 8, 2025 (HealthDay News) — Many more folks fighting excess weight are using weight-loss drugs like Ozempic or Zepbound to cut pounds before undergoing bariatric surgery, a new study says. The use of these drugs before surgery rose 16-fold among patients preparing for weight-loss surgery, researchers reported Sunday at the American College of Surgeons’ annual meeting in Chicago. “While patients previously believed they had to choose between GLP-1 receptor agonists and surgery, we’re now seeing that people are using both,” said lead researcher Dr. Stefanie Rohde, a general surgery resident at the Ohio State University Wexner Medical Center in Columbus. “We know that patients can use GLP-1s after bariatric surgery to amplify their weight loss,” Rohde said in a news release. “But all of this is still very new in terms of how to manage patients effectively.” For the study, researchers looked at the ...
CanSino’s independently developed 13-valent pneumococcal polysaccharide conjugate vaccine PCV13i and Asia’s first quadrivalent meningococcal polysaccharide conjugate vaccine MCV4 were shipped to the domestic and overseas markets respectively. CanSino Biologics’ independently developed 13-valent pneumococcal polysaccharide conjugate vaccine, Upexin®, was officially approved by the National Medical Products Administration in June of this year. It is China’s first pneumococcal polysaccharide conjugate vaccine to utilize a dual vector consisting of an avirulent mutant of diphtheria toxin (CRM197) and tetanus toxoid (TT). This vaccine provides enhanced protection against the four serotypes (19F, 19A, 7F, and 3) that carry the heaviest burden of pneumococcal disease in children in China. It is reported that by 2026, Upexin® will expand its reach into the domestic market, with overseas expansion also in the works. When Youpexin® was shipped domestically, Asia’s first ACYW135 group meningococcal polysaccharide conjugate vaccine (CRM197 vector) Manhaixin® also departed from Tianjin and was sent to Indonesia. ...
Changchun High-techChangchun High-Tech Industry (Group) Co., Ltd. (hereinafter referred to as ” Changchun High-Tech “) issued an announcement stating that its subsidiary Changchun Jinsai Pharmaceutical Co., Ltd. (hereinafter referred to as “Jinsai Pharmaceutical”) recently received the “Drug Registration Certificate” approved and issued by the State Food and Drug Administration. Its application for the choriofollicle-stimulating hormone αN02 injection has been approved for marketing in China. The approved indication is for use in combination with a gonadotropin-releasing hormone antagonist for controlled ovarian stimulation to induce the development of multiple follicles. A single subcutaneous injection of choriofollicle-stimulating hormone αN02 injection (Jinsaijia®) replaces the 7-day use of follicle-stimulating hormone for assisted reproduction .Ovarian stimulation therapy brings new options. In recent years, demand for assisted reproductive technology has continued to grow. In 2015, Jinsai Pharmaceutical launched the first domestically developed recombinant human follicle-stimulating hormone (RFH) for injection (Jinsai Heng®). This short-acting formulation, administered daily, was ...
After the U.S. stock market opened on Tuesday, Pfizer, which has been deeply affected by the uncertainty of U.S. pharmaceutical policies this year,The company’s stock price rose by over 4% at one point. Multiple sources indicate that Pfizer CEO Albert Bourla will visit the White House later on Tuesday to announce drug pricing policies and a $70 billion domestic investment plan with Trump. ( Pfizer daily chart, Source: TradingView) In addition to Pfizer, many large pharmaceutical companies also rose .Bristol-Myers Squibb rose nearly 3%.Up 2%, AmgenUp 1%. If the news is true, Pfizer has resolved at least two policy uncertainties : US President Trump once wrote to Pfizer and 16 other pharmaceutical companies asking for price cuts, and demanded that prices in the United States should not be more expensive than those in developed countries such as Europe (the “most favored nation” policy); Trump also announced tariffs on branded drugs last ...
According to foreign media reports, Biogen has terminated all gene therapy projects based on adeno-associated virus (AAV) capsids. In fact, Biogen deprioritized gene therapy as early as 2023. Now, as part of its ongoing capital allocation strategy, the company will completely abandon AAV technology. Biogen is a biotechnology company with deep expertise in rare and genetic diseases. The company said it will continue to focus on this area in the future and concentrate its resources on advanced therapies and drugs that have greater potential and are more likely to bring better therapeutic effects to patients. Most of the team members who were previously responsible for AAV vector research and development have been reassigned to other positions within the company, but a small number of people are still facing layoffs, involving R&D, operations, technology and other positions. Biogen is not the first company to abandon AAV technology. AAV (adeno-associated virus) is ...
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