Recently, Gilead announced that the European Commission (EC) has conditionally approved Seladelpar for marketing in combination with ursodeoxycholic acid (UDCA) to treat patients with primary biliary cholangitis (PBC) who have an insufficient response to UDCA alone; or as a single drug to treat PBC patients who are intolerant to UDCA treatment. Seladelpar is the first and only therapy to achieve significant improvements in biochemical responses, alkaline phosphatase normalization, and pruritus relief compared to placebo. This approval means that patients with rare liver diseases in the European Economic Area (EEA) will have an important new treatment option. From the MASH dilemma to the PBC breakthrough, Seladelpar’s research and development journey has been full of twists and turns. Originally developed by CymaBay, in 2006, Johnson & Johnson and CymaBay Therapeutics reached a comprehensive development and commercialization agreement on metabolic disease drugs, and Johnson & Johnson obtained the licensing rights for three drugs ...
Organiser:Informa Markets Time:September 1st – 3rd, 2025 Address:El-Nasr Rd, Al Estad, Nasr City, Cairo Governorate Exhibition hall:Cairo International Convention Centre Product range: Vitamins, Hormones, Antipyretic and Analgesic Drugs, Medications for Digestive System, Anti-infective Drugs, Antiparasitic Drugs, Cardiovascular System Drugs, Intermediates Pharmaceutical Packaging Materials, PVC/PVDC Laminates, PVC Rigid Sheets, PS Sheets, Packaging Anti-counterfeiting Technology, Sleeve Labeling Techniques, Labeling Machines, Packaging Containers, Form-Fill-Seal Machines, Wrapping Machines, Paper Film Packaging Machinery, Bag Packaging Machines, etc. Infusion Equipment Production Lines, Dryers, Water Treatment Equipment, Refrigeration Compressors, Distillation Equipment, Sterilization Equipment, Tablet Press Machines, Coating Machines About Pharmaconex: Pharmaconex, the Pharmaceutical Ingredients and Technologies Exhibition in Cairo, Egypt, is the most renowned exhibition dedicated to pharmaceutical ingredients and technologies in the country. It is organized by Informa Markets, a prestigious exhibition company in the UK, with extensive experience and strong capabilities in organizing exhibitions. The event holds significant importance for exploring the Egyptian ...
Recently, Elekta (EKTA-B.ST) announced that its President and CEO, Gustaf Salford, and board of directors have unanimously decided to resign on March 6th. The board of directors of Yikeda is conducting international recruitment for the position of new CEO. During this period, the board has appointed Jonas Bolander, Executive Vice President, General Counsel, and Group Functional Head with 23 years of experience at Medda, as Acting President and CEO. 01. Net profit decreased by 30% For the nine months ending January 31, 2025, Elekta achieved revenue of 12.86 billion Swedish kronor and a net profit of 621 million Swedish kronor. Compared to the same period last year, net profit decreased by 30% and revenue decreased by 2%. In the latest Medical Technology Top 100 Report, it ranks 56th in annual revenue. Dr. Laurent (Larry) Leksell, Chairman of the Board, stated, “Although Elekta’s mid-term performance in the third quarter did not ...
Every year’s Rare Disease Day is an important moment for us to pay attention to these ‘minority groups’. For rare disease patients, the development and approval of new drugs mean hope for life. In recent months, the China National Medical Products Administration’s Center for Drug Evaluation (CDE) has prioritized the evaluation of multiple rare disease drugs, including symptomatic giant cell tumors of the tendon sheath, myasthenia gravis, giant cell arteritis, idiopathic pulmonary fibrosis, and other indications. These drugs are expected to accelerate approval and bring new treatment options to patients. This article will review the research and development progress of 7 new drugs based on publicly available information, hoping that they will be launched soon and light up the future for rare disease patients. According to the official website of CDE, since September 2024, CDE has added a “rare disease drug” label to new drugs included in priority review. This ...
Recently, Hengrui Pharmaceutical has lost its position as the “top pharmaceutical company”. On February 21st, the A-share pharmaceutical sector ushered in a historic turning point – at the closing price, BeiGene surpassed Hengrui Pharmaceutical’s 308 billion yuan market value with a market value of 310.7 billion yuan, and for the first time topped the A-share pharmaceutical company market value list with a slight advantage of 2.7 billion yuan, overturning Hengrui Pharmaceutical’s long-standing position as the “top pharmaceutical company”. BeiGene’s transcendence sends a signal. For a long time in the past, Hengrui Pharmaceutical was undoubtedly the leader in the pharmaceutical industry. With its “imitation+innovation” model, Hengrui has been leading the entire industry, and its multiple core products once occupied half of the domestic pharmaceutical market. As early as 2021, the stock price of Hengrui Pharmaceutical continued to rise after a continuous surge, reaching a peak of 96.7 yuan per share, with ...
NO.1 Support qualified traditional Chinese medicine and other biopharmaceutical companies to issue and list on the Shanghai and Shenzhen stock exchanges The China Securities Regulatory Commission has issued a letter in response to Proposal No. 4171 (Finance, Taxation, and Finance 261) of the Second Session of the 14th National Committee of the Chinese People’s Political Consultative Conference. Among them, it is mentioned that actively supporting qualified biopharmaceutical companies, including traditional Chinese medicine, to issue and list on the Shanghai and Shenzhen stock exchanges, focusing on expanding direct financing channels for biopharmaceutical companies, and fully leveraging the supportive role of the capital market in the development of the biopharmaceutical industry. Commentary: The China Securities Regulatory Commission supports the listing of traditional Chinese medicine and other biopharmaceutical companies, expanding direct financing channels. This move will help promote innovative development in the biopharmaceutical industry, enhance the support of the capital market for the ...
Robert Kennedy, Secretary of the U.S. Department of Health and Human Services, said he was aware of the serious impact of the current measles outbreak in Texas, and ending the measles outbreak was the top priority for him and his team. The U.S. Department of Health and Human Services will provide 2,000 doses of measles, mumps and rubella vaccines to Texas through its immunization program. According to data from the U.S. Centers for Disease Control and Prevention (CDC) on February 27, 164 measles cases have been reported in the United States, an increase of nearly 80% from the 93 cases reported a week ago. Of these cases, about 95% were from unvaccinated people, and another 3% were from people who had only received one dose and had not completed all immunizations. https://finance.eastmoney.com/a/202503013333801648.html
On the evening of February 28, Kangleweishi issued an announcement stating that on the same day, the independent data monitoring committee (IDMC) of the domestic phase III protective efficacy clinical trial of the company’s independently developed recombinant nine-valent human papillomavirus (6/11/16/18/31/33/45/52/58) vaccine (Escherichia coli) (female indication) has completed the first analysis unblinding, primary efficacy indicators and safety evaluation, and the company has received the IDMC’s recommendation letter based on the first analysis results. The company stated that the independent data monitoring committee (IDMC) confirmed that the efficacy results met the first analysis statistical criteria preset in the protocol. The first analysis results of the company’s nine-valent HPV vaccine (female indication) domestic phase III protective efficacy clinical trial were in line with expectations, marking a major progress in the clinical research of the nine-valent HPV vaccine. The company said the development is not expected to have a material impact on its ...
Rabies vaccine leader Chengda Bio (688739.SH) recently disclosed its performance report. In 2024, the company achieved operating income of 1.676 billion yuan, a year-on-year decline of 4.22%; and achieved a net profit attributable to the parent of 334 million yuan, a year-on-year decrease of 28.4%. This is the fourth consecutive year that Chengda Bio’s net profit has declined since its listing on the Science and Technology Innovation Board in 2021. Although the company has dominated the domestic human rabies vaccine market for 16 consecutive years since 2008, as more challengers have entered the market, its market share has fallen from more than 70% at its peak to less than 40% in 2024. In recent years, Chengda Bio has tried to find a second growth line, but with little success. The Japanese encephalitis inactivated vaccine launched in 2008 has accounted for less than 10% of the company’s revenue so far, and ...
Recently, Sinocell released its 2024 performance report, and the results are quite impressive. In 2024, Sinocell’s total operating revenue was 2.513 billion yuan, a year-on-year increase of 33.13%. Operating profit reached 568 million yuan, a year-on-year increase of 8829.33%, and the net profit attributable to the parent company’s owners was 112 million yuan, successfully turning losses into profits. In addition, the non-net profit also reached 474 million yuan, also turning losses into profits. 1 2 billion single product Sinocell is a leading innovative biopharmaceutical R&D and industrial development company founded by Dr. Xie Liangzhi, an internationally renowned biopharmaceutical expert. The company was listed on the Science and Technology Innovation Board in 2020, and launched its first listed product, recombinant human coagulation factor VIII for injection (Anjiayin) in 2021. In 2024, the company finally turned losses into profits. According to the announcement of Sinocell, the company’s total operating income in 2024 ...
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