media – Page 15 – Pharma & Medical Industry Insights Hub | Drugdu Insights & Updates

Fierce battle for acetylcysteine tablets! Huayi Pharmaceutical’s entry accelerates market differentiation

On June 17, according to the latest announcement on the CDE official website: Huayi Pharmaceutical’s application for the listing of the Class 3 generic drug acetylcysteine tablets was accepted, making it the eighth Chinese pharmaceutical company to enter this dosage form. This move has caused new waves in the acetylcysteine market. from Tidu , the sales of acetylcysteine tablets in all terminals have been growing in recent years. In 2024, the sales of all terminals exceeded 389 million yuan, a year-on-year increase of more than 13%. In the entire expectorant market, acetylcysteine has topped the list for four consecutive years with a share of over 50%. Acetylcysteine tablets are a commonly used expectorant in clinical practice. By decomposing the disulfide bonds of mucin in sputum, it effectively reduces the viscosity of sputum and promotes the discharge of sputum. In clinical practice, it is mainly used to treat symptoms such as ...
- Source: drugdu
- 133
- June 24, 2025
Lianya Pharmaceuticals opens up a new path to accelerate the export of domestic high-end preparations and domestic supply

The quality of drug preparations is directly related to the life, health and treatment effects of hundreds of millions of patients. At present, China is the world’s second largest pharmaceutical market. It is reported that the total output value of China’s pharmaceutical industry will reach about 3.8 trillion yuan in 2022, and generic drugs will dominate the Chinese pharmaceutical market, accounting for more than 60%. However, in the field of high-end generic drugs, especially in sustained-release preparations and complex injections, there are high technical barriers, and the market accessibility of domestic high-end generic preparations is relatively low. The root cause is the weakness of the core production process, especially the precise control of the drug release mechanism, the application of complex excipient systems, and the precision quality control technology in large-scale production, which has become a key bottleneck restricting domestic high-end preparations from achieving equivalence with original research drugs and ...
- Source: drugdu
- 133
- June 24, 2025
Guangzhou International High-end Medical Devices Exhibition

Organiser: China Association for Medical Devices Industry (CAMDI) Time：July 17 – 19, 2025 address：No. 1108, Yingbin Avenue, Baiyun District, Guangzhou City, Guangdong Province Exhibition hall：Guangzhou Airport Expo Center Product range: Medical Imaging: CT, DR, medical X-ray systems, ultrasonic diagnostic instruments, magnetic resonance equipment, tumor treatment machines, medical films and processing systems, medical 3D printing devices, etc. Remote, Mobile, and Intelligent Monitoring Medical Devices: Sleep monitors, remote ECG, blood pressure, blood oxygen, and body temperature detectors, cloud blood pressure meters, Bluetooth blood pressure and blood glucose monitors, wearable medical devices, and health kiosks; Mobile Medical: Telemedicine, APPs, big data cloud platforms, physical examination, rehabilitation, and medical diagnostic and treatment equipment. Diagnostic and Therapeutic Equipment: Endoscopic systems, otorhinolaryngological instruments, dynamic analysis instruments, cryogenic freezing equipment, dialysis treatment equipment, emergency rescue equipment, etc. Surgical Instruments: Electrosurgical units and consumables, staplers, suture devices, suture needles/threads, laser surgical instruments, ultrasonic surgical devices, equipment and ...
- Source: drugdu
- 129
- June 24, 2025
Zhengda Tianqing’s bispecific ADC is approved for clinical trials, and the competition for EGFR/c-Met targets heats up again

Recently, the official website of the Center for Drug Evaluation (CDE) of the China National Drug Administration showed that the TQB6411 injection, a Class 1 innovative drug independently developed by Zhengda Tianqing, has been approved for clinical use and is intended to be used to treat patients with advanced malignant tumors. As a dual-antibody ADC (antibody-drug conjugate) targeting EGFR/c-Met, this drug has become a “new species” that has not yet been approved for marketing in the world. The design logic of TQB6411 directly targets the key pain points of tumor treatment – drug resistance and compensatory activation of signal pathways. Epidermal growth factor receptor (EGFR) and mesenchymal epithelial transition factor (c-Met) are driver genes for various tumors such as lung cancer and colorectal cancer, and often form synergistic effects in signal transduction. When a drug inhibits only one of the pathways, the other pathway may be compensatorily activated, resulting in ...
- Source: drugdu
- 97
- June 23, 2025
New bispecific antibody company plans to go public in Hong Kong

In the biotechnology field, bispecific antibodies are becoming game-changing innovative therapeutics. On June 17, 2025, the Hong Kong IPO application of Innovent Biologics, a pioneer in the next-generation bispecific antibodies, was accepted and the prospectus was officially released. Founded in 2015, EpiMed Biopharma has been focused on developing bispecific antibodies using its proprietary bispecific antibody platform since its inception. Its strategic focus is on the field of T cell engagers, focusing on two major disease areas: tumors and autoimmune diseases. EpiMed has developed a proprietary technology platform designed to overcome the limitations of traditional bispecific antibody development: FIT-Ig platform: It has a unique linker-free, non-mutational and tetravalent bispecific antibody platform that can quickly generate bispecific antibody molecules while maintaining the biological function of each antibody domain, thereby achieving plug-and-play for multiple different targets. The FIT-Ig platform is the only bispecific antibody technology in the world that does not require any ...
- Source: drugdu
- 91
- June 23, 2025
Connoya sprints to become the “King of Chinese Self-immunity”

Recently, NEJM published the breakthrough data of Conoya’s BCMA/CD3 dual antibody CM336 in the treatment of refractory autoimmune hemolytic anemia (AIHA), with significant and lasting efficacy. This is not only a strong proof of its innovative strength, but also forms a synergy with the rapid commercialization of its trump card CM310, strongly supporting its sprint to become the king of autoimmune in China. BCMA/CD3 dual antibody autoimmune new blue ocean Bispecific antibody technology with T cell redirection as the core mechanism has made significant breakthroughs in the field of hematological tumors. Among them, BCMA/CD3 bispecific antibodies effectively guide cytotoxic T lymphocytes (CTL) to target and kill tumor cells through their unique dual antigen binding ability. Globally, two drugs, Teclistamab from Johnson & Johnson and Elranatamab from Pfizer, have been approved for relapsed and refractory multiple myeloma (RRMM). The former will land in the Chinese market in June 2024. Johnson & ...
- Source: drugdu
- 58
- June 23, 2025
Is It Worth Adding Chemo to ICI for NSCLC in Older Adults?

Immune checkpoint inhibitors (ICI) are a cornerstone of non-small cell lung cancer (NSCLC) treatment, but it’s not clear whether adding chemotherapy to ICI — a common practice with younger patients with NSCLC — helps older ones. No randomized trial has directly compared stand-alone ICI with chemoimmunotherapy in geriatric patients with NSCLC. Without strong data supporting the combined approach, oncologists may stay away from offering chemoimmunotherapy to older patients, especially to those with multiple comorbidities, given concerns about increased toxicity. To address the evidence gap, investigators linked Medicare and Surveillance, Epidemiology, and End Results data to compare outcomes between 14,249 older patients with NSCLC who received ICI alone (pembrolizumab or nivolumab) and 3432 treated with ICI and platinum doublet chemotherapy. Patients were aged 74 years, on average, and at least 66 years. The median follow-up duration was 211 days. The team weighed the risks and benefits of chemoimmunotherapy vs stand-alone ...
- Source: drugdu
- 52
- June 23, 2025
The World’s Only Twice-A-Year Shot to Prevent HIV Could Stop Transmission — if People Can Get It

WASHINGTON (AP) — The U.S. has approved the world’s only twice-a-year shot to prevent HIV, the first step in an anticipated global rollout that could protect millions – although it’s unclear how many in the U.S. and abroad will get access to the powerful new option. While a vaccine to prevent HIV still is needed, some experts say the shot made by Gilead Sciences — a drug called lenacapavir — could be the next best thing. It nearly eliminated new infections in two groundbreaking studies of people at high risk, better than daily preventive pills they can forget to take. “This really has the possibility of ending HIV transmission,” said Greg Millett, public policy director at amfAR, The Foundation for AIDS Research. Condoms help guard against HIV infection if used properly but what’s called PrEP — regularly using preventive medicines such as the daily pills or a different shot ...
- Source: drugdu
- 57
- June 23, 2025
【EXPERT Q&A】What are the characteristics of the medical device industry?

Drugdu.com expert’s response: The medical device industry is characterized by its interdisciplinary nature, knowledge-intensive and capital-intensive requirements, stringent regulation, substantial market potential, low industry concentration, and fierce competition. The details are as follows: Interdisciplinary Nature: It encompasses disciplines such as engineering, medicine, physics, biology, materials science, computer science, human-computer interaction, and aesthetics, resulting in a high R&D threshold. Knowledge-Intensive and Capital-Intensive: It is a typical technology-intensive industry, with its development highly reliant on continuous technological R&D and innovation, necessitating significant capital investment. For instance, the initial funding for a medium-sized medical device project can reach as high as 30 million yuan. Stringent Regulation: It is subject to strict laws and regulations. The R&D, production, distribution, and use of medical device products must comply with relevant national standards, industry standards, and regulatory requirements, with complete and traceable records required throughout the product lifecycle. Substantial Market Potential: Driven by factors such as ...
- Source: drugdu
- 122
- June 23, 2025
Are Pre-Workout Powders Overloading the Heart?

Pre-workout supplements are gaining popularity in Brazil because of their promising effects, including increased focus, energy, endurance, enhanced performance, and reduced muscle fatigue. A growing number of brands are now available in specialty stores, pharmacies, and supermarkets. However, with so many options in the market, are consumers aware of the risks and product components, and do these products benefit physical performance? Typically sold in powdered soluble form, but also available as capsules, gummies, gels, or ready-to-drink liquids, pre-workout supplements combine various substances, such as caffeine, beta-alanine, arginine, taurine, and creatine, with formulas that vary by brand. “Pre-workout [supplements] usually have a combination of multiple elements, such as vitamins, proteins and amino acids, but only a very small portion actually have any effect with proven scientific evidence on sports performance,” said Cristiano Barcellos, PhD, director of the Department of Sports and Exercise Endocrinology at the Brazilian Society of Endocrinology and Metabolism. ...
- Source: drugdu
- 80
- June 20, 2025

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