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Zai Lab’s Phase III clinical trial of this drug achieved positive results

On June 30, Zai Lab announced that the main data of the Phase III study of bemazumab for FGFR2b-positive first-line gastric cancer achieved positive results . Zai Lab said that the detailed results of the study will be announced at a future medical conference, but this achievement is expected to redefine the standard treatment of first-line gastric cancer and bring new hope of survival to gastric cancer patients. 01 New breakthrough The FORTITUDE-101 study is a global multicenter, randomized, double-blind, placebo-controlled clinical trial designed to evaluate the efficacy and safety of bematuzumab combined with mFOLFOX6 chemotherapy versus placebo combined with mFOLFOX6 as first-line treatment. The study was conducted in 300 research centers in 37 countries around the world, with a total of 547 patients enrolled. The study met its primary endpoint of overall survival (OS) at a pre-specified interim analysis, with bematumab plus chemotherapy demonstrating a statistically significant and clinically ...
- Source: drugdu
- 133
- July 3, 2025
The first domestic generic version of Lifelast Eye Drops (5%) was approved for marketing

On June 30, the official website of the National Drug Evaluation Center showed that Kanghong Pharmaceutical’s lifetilast eye drops (trade name Langyueming) were exclusively launched in China as a Class 3 new drug, which will provide a new option for dry eye treatment. With the popularization of electronic devices, the acceleration of the aging process and bad eye habits, the incidence of dry eyes in China has been increasing year by year. The number of people suffering from dry eyes or dry eye symptoms in China exceeds 300 million. According to a research report by the China Economic Industry Research Institute, the domestic dry eye drug market will reach 4.79 billion yuan in 2024, with a compound growth rate of 16.17% from 2020 to 2024, providing a huge market space for the development of dry eye drugs. Inflammatory response is the driving factor of ocular surface damage in the pathological ...
- Source: drugdu
- 132
- July 3, 2025
Arab Health

Organiser: Informa Group Time：February 9-12, 2026 address：Sheikh Zayed Road, Trade Centre – Trade Centre 2, Dubai, United Arab Emirates Exhibition hall：Dubai World Trade Centre Product range: Medical Devices and Instrumentation: Medical electronic instruments, medical ultrasonic instruments, medical X-ray equipment, medical optical instruments, clinical laboratory analytical instruments, dental equipment and materials, operating room/emergency room/consultation room equipment and appliances, disposable medical supplies, medical dressings and hygienic materials, various surgical instruments, medical wellness devices and supplies, traditional Chinese medical instruments and rehabilitation aids, hemodialysis equipment, anesthesia and respiratory equipment, etc. Home Healthcare Products and Portable Wellness Devices: Home health and wellness products, portable diagnostic, monitoring, and therapeutic instruments, rehabilitation/physical therapy devices and supplies, electronic medical instruments, dental tools, hospital office supplies, sports medicine products. Active Pharmaceutical Ingredients (APIs), Traditional Chinese Medicines, and Health Supplements: Therapeutic, rehabilitative, and wellness pharmaceuticals and products rooted in Eastern medical traditions. About Arab Health： The Arab Health ...
- Source: drugdu
- 133
- July 3, 2025
【EXPERT Q&A】How is medical device software recognized and classified in the European Union?

Drugdu.com expert’s response: I. How to Determine if a Software is Medical Device Software? In simple terms, for the European Union (EU), a software is considered medical device software (MDSW) when it meets three conditions simultaneously: It Performs Medical Tasks For example, diagnosing diseases, monitoring conditions, treating patients, or assisting in surgeries. If it merely records exercise steps, reminds users to drink water, or sends notifications to doctors (without involving medical decision-making), it doesn’t qualify. Examples: A software that analyzes electrocardiogram (ECG) data to assess heart disease risk is medical device software; a fitness app that records daily step counts is not. It Processes Data The software should not just store or display data (such as an electronic medical record system). It must analyze, calculate, modify the data, and then generate medical-related results. Examples: A software that automatically marks tumor locations based on computed tomography (CT) images is medical device ...
- Source: drugdu
- 143
- July 2, 2025
Apple may abandon its self-developed AI models; Zuckerberg announces restructuring of Meta AI team | Global technology early participation

NO.1 Apple may abandon self-developed AI models According to foreign media sources, Apple is considering abandoning its self-developed internal model and using Anthropic or OpenAI’s artificial intelligence (AI) technology to drive the new version of Siri. Insiders revealed that Apple has contacted these two companies to discuss deploying their Large Language Model (LLM) on Apple’s own cloud infrastructure for testing. Comment: This collaboration may indicate that Apple’s self-developed progress in the AI field is not as expected and requires external forces to accelerate development. NO.2 Moderna Influenza Vaccine Phase III Clinical Trial Successfully Completed On Monday, US vaccine manufacturer Moderna announced that its experimental influenza vaccine based on mRNA had a stronger immune response than the existing vaccine in a phase III trial, which paved the way for the approval of its COVID-19/influenza combined vaccine. Comment: This achievement not only brings new hope to the influenza vaccine market, but ...
- Source: drugdu
- 205
- July 2, 2025
The Hang Seng Hong Kong Stock Connect Innovative Drug Index is about to be revised; Hengrui Pharmaceutical’s alopecia areata drug has been approved for market launch | Medical Early Reference

NO.1 Hang Seng Hong Kong Stock Connect Innovative Drug Index is about to be revised, explicitly excluding CXO companies On June 30th, the Hang Seng Hong Kong Stock Connect Innovation Drug Index announced a revised compilation plan, adding a rule to exclude CXO (pharmaceutical outsourcing) companies. According to the new compilation plan, all the constituent stocks of the revised index are innovative pharmaceutical companies, making it one of the first innovative pharmaceutical indices tracked by ETFs to achieve a purity of 100%. Pang Yaping, General Manager of the Index Research Department of E Fund, stated that CXO mainly provides services and does not directly acquire the core intellectual property rights of innovative drugs. Generally, CXO does not participate in the patent development and commercialization of innovative drugs and does not obtain patent authorization benefits. Therefore, after excluding CXO, the Hang Seng Hong Kong Stock Connect Innovative Drug Index can focus ...
- Source: drugdu
- 482
- July 2, 2025
FDA Approves Benlysta Autoinjector for Pediatric Patients With Active Lupus Nephritis

By Lori Solomon HealthDay ReporterMONDAY, June 30, 2025 (HealthDay News) — The U.S. Food and Drug Administration has approved an autoinjector of Benlysta (belimumab) for subcutaneous injection in patients ≥5 years of age with active lupus nephritis who are receiving standard therapy. Benlysta (200 mg/mL), a B-lymphocyte stimulator-specific inhibiting monoclonal antibody, is the first and only approved biologic for both systemic lupus erythematosus and lupus nephritis. It is not recommended in patients with severe active central nervous system lupus. The most common major adverse reactions seen with Benlysta were serious infections, some of which were fatal. The most common adverse reactions (≥5 percent) were nausea, diarrhea, fever, inflammation of the nasal passages and throat, bronchitis, insomnia, pain in extremity, depression, migraine, and injection site reactions. “In children, lupus tends to be more aggressive and severe than it is in adults. The symptoms can be more intense, and the disease ...
- Source: drugdu
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- July 2, 2025
‘Pill-On-A-String’ Could Revolutionize Testing For Throat Cancer

By Dennis Thompson HealthDay ReporterMONDAY, June 30, 2025 (HealthDay News) — The thought of swallowing a pill on a thread isn’t the most pleasant notion, but it could be a vastly better alternative for people at increased risk of throat cancer, a new study says. For nearly 20 years, U.K. resident Duncan Cook has had regular endoscopies to monitor his case of Barrett’s esophagus, a condition in which acid reflux damages cells and can lead to throat cancer. Then researchers offered him another option: Swallow a capsule that dissolves in the stomach to release a small sponge. Using an attached string, health care professionals draw the sponge back up the throat, lightly scraping cells off the esophagus along the way. “The first time I had the sponge, I was a bit nervous. It’s quite a big pill to swallow, but it’s much better than going for endoscopies,” Cook, 57, ...
- Source: drugdu
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- July 2, 2025
Hybribio obtained 1 invention patent

July 1, Hybribio(300639) announced that the company and its subsidiaries have recently obtained authorization for an invention patent. The patent is called “Method, device and equipment for processing genome copy number variation analysis data”, the patent number is 202510354669.9, and the country of grant is China. The patent holders include Guangzhou Cap Medical Laboratory Co., Ltd., Guangzhou Cap Medical Laboratory Development Co., Ltd. and the company itself. The invention relates to the field of bioinformatics and provides a data screening logic and conditions that can accurately present the CNV results of the whole genome. This method can reduce interference information and improve the accuracy and readability of the interpretation of the test results. The company said that obtaining this patent is in line with its development strategy and will not have a significant impact on the current business situation, but it will help improve intellectual property rights.system to enhance core ...
- Source: drugdu
- 158
- July 2, 2025
RecBio and India’s Biological E company reached a product licensing cooperation on the recombinant nine-valent HPV vaccine

On June 30, RecBio announced that the company and Indian Biological ProductsBiological E (hereinafter referred to as “BE Company”) signed a product licensing cooperation agreement for the recombinant nine-valent HPV vaccine REC603. RecBio will transfer vaccine formulation and subpackaging technology to BE, and transfer stock solution production technology at an appropriate time. According to the agreement, BE is exclusively authorized to develop, produce and commercialize recombinant nine-valent HPV vaccines in India and the bidding market led by the United Nations Children’s Fund (UNICEF) and the Pan American Health Organization (PAHO). At present,RecBio has received an advance payment for the cooperation and will receive milestone payments according to the progress of the cooperation, as well as royalties based on a certain percentage of annual net sales. https://finance.eastmoney.com/a/202506303443960124.html
- Source: drugdu
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- July 2, 2025

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