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Bristol-Myers Squibb’s Opdivo-Yervoy Combo Nears FDA Approval for MSI-H Colorectal Cancer
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Bristol-Myers Squibb (BMS, NYSE: BMY) announced that the U.S. FDA has accepted its filing for Opdivo (nivolumab) combined with Yervoy (ipilimumab) as a first-line treatment for adult and pediatric patients (aged 12+) with unresectable or metastatic microsatellite instability-high (MSI-H) or mismatch repair deficient (dMMR) colorectal cancer (mCRC). The FDA set…
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CanSino Biologics Receives NMPA Approval for DTcP Hib MCV4 Combined Vaccine
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China-based vaccine specialist CanSino Biologics Inc. (HKG: 6185) announced that its absorbed diphtheria, tetanus, acellular pertussis (DTcP), Haemophilus influenzae type b (Hib), and Group ACYW135 meningococcal (MCV4) combined vaccine has received clinical trial approval from the National Medical Products Administration (NMPA). The single-dose vaccine aims to provide comprehensive immune protection…
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MGI Tech Partners with Oncoclínicas&Co to Advance Precision Medicine in Brazil
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China-based gene sequencing specialist MGI Tech Co., Ltd (SHA: 688114) has partnered with OC Medicina de Precisão of Oncoclínicas&Co, Latin America’s largest cancer treatment group. The collaboration aims to promote precision medicine innovation in Brazil, offering efficient and personalized cancer diagnosis and treatment. Partnership DetailsThe partnership combines OC Medicina de…
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Boehringer Ingelheim’s Nerandomilast Receives NMPA Review for IPF Treatment
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Boehringer Ingelheim announced that its investigational drug nerandomilast has been accepted for review by the Center for Drug Evaluation (CDE) of China’s National Medical Products Administration (NMPA). The German pharma giant seeks approval for the oral phosphodiesterase 4B (PDE4B) inhibitor to treat idiopathic pulmonary fibrosis (IPF) in adults. Clinical Trial…
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QYuns Therapeutics’ QX002N Meets Primary Endpoint in AS Phase III Study
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China-based Jiangsu QYuns Therapeutics Co., Ltd (HKG: 2509) announced that its Phase III study of QX002N, an anti-IL-17A monoclonal antibody, in ankylosing spondylitis (AS) has met its primary endpoint. The multi-center, randomized, double-blinded, placebo-controlled trial enrolled 641 patients with moderate to severe AS. Study Results
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Takeda’s Takhzyro Receives EMA Approval for New Administration Form in HAE Patients
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Japan-headquartered Takeda (NYSE: TAK, TYO: 4502) announced that the European Medicines Agency (EMA) has approved a label extension for Takhzyro (lanadelumab) for subcutaneous administration in adolescents aged 12 and above and adult patients with Hereditary Angioedema (HAE) using a 2 mL pre-filled pen. Drug ProfileTakhzyro is now approved in the…
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Ipsen Posts 8.7% Revenue Growth in 2024, Driven by Rare Diseases and Oncology
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French biopharma firm Ipsen (EPA: IPN, OTCMKTS: IPSEY) reported an 8.7% year-on-year (YOY) increase in global revenues to €3.4 billion ($3.57 billion) for 2024, according to its annual financial report. Core operating profit rose 10.8% YOY to €1.109 billion ($1.165 billion), driven by strong performances across all business sectors. Sector…
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Meyer FSMP Hong Kong Secures NMPA Approval for First FSMP in Greater China
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Hong Kong-based Meyer FSMP Hong Kong Limited, an oncology-focused foods for special medical purpose (FSMP) company, announced it has received marketing approval from China’s National Medical Products Administration (NMPA) for its carbohydrate component formula. The product is the first FSMP approved in the Hong Kong, Macao, and Taiwan regions. Product…
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Pfizer Halts Global Development of Hemophilia B Gene Therapy Beqvez Amid Limited Demand
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Pfizer Inc. (NYSE: PFE) has terminated the development and commercialization of Beqvez (fidanacogene elaparvovec), its hemophilia B gene therapy, globally, citing “limited interest” from patients and physicians, according to reports in Nikkei Asia and Reuters. The move marks the U.S. pharma giant’s exit from virally delivered gene replacement treatments. Decision…
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Jointown Pharmaceutical Partners with Shandong DYNE to Boost Pediatric Drug Distribution
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Jointown Pharmaceutical Group Co., Ltd (SHA: 600998), China’s largest private pharmaceutical distributor, has partnered with Shandong DYNE Marine Biopharmaceutical Co., Ltd., a state-owned firm specializing in pediatric medications. The collaboration aims to integrate Jointown’s nationwide logistics network with DYNE’s R&D expertise in pediatric drugs. Jointown’s Distribution EdgeJointown operates a logistics…
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CSPC Pharmaceutical Initiates Phase III Trial for Ammuxetine in Depression Treatment
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China-based CSPC Pharmaceutical Group Ltd (HKG: 1093) announced the start of a Phase III clinical trial for its Category 1 chemical drug ammuxetine at the Shanghai Mental Health Center, a top-tier Class 3A mental hospital. Drug ProfileAmmuxetine, a small molecule SNR inhibitor discovered by the Chinese Academy of Military Medical…
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Subtle Medical Integrates DeepSeek with FDA-Approved SupMR AI Platform
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Shanghai-based Subtle Medical Inc., an AI-powered medical imaging firm operating in the U.S. and China, announced FDA approval for the updated version of its SupMR generative AI image enhancement technology. The upgraded platform delivers significant improvements in MRI image quality, speed, and efficiency. Technology HighlightsThe new SupMR AI leverages the…
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AWS Collaborates with MSK to Accelerate Oncology Research via AI and Cloud Tech
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Amazon Web Services (AWS) announced a strategic collaboration with Memorial Sloan Kettering Cancer Center (MSK), a world-leading cancer research institute based in New York. The partnership aims to leverage artificial intelligence (AI), high-performance computing (HPC), and cloud technologies to drive breakthroughs in oncology research and personalized treatment development. Collaboration DetailsAWS…
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Cholesgen Raises Over RMB100M in Series A to Advance Metabolic Disease Pipelines
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China-based glycolipid metabolism specialist Cholesgen (Shanghai) Co. Ltd. has reportedly raised over RMB100 million ($13.8 million) in a Series A financing round led by SDIC. The AstraZeneca-CICC Medical Industry Investment Fund, an existing investor, also participated. The proceeds will fund clinical filings, development of core pipelines, and expansion of the…
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Innorna’s IN013 Receives FDA Rare Pediatric Designation for Wilson’s Disease Treatment
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Shenzhen-based Innorna Co., Ltd, a platform company leveraging mRNA and lipid nanoparticle (LNP) delivery technologies, announced that its IN013 has received Rare Pediatric Disease Designation (RPDD) from the U.S. Food and Drug Administration (FDA). The mRNA drug is designed to treat hepatolenticular degeneration (HLD), also known as Wilson’s disease, a…
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Amoytop Biotech to Acquire Skyline Therapeutics’ Gene Therapy Assets for $15M Plus Milestones
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Xiamen-based Amoytop Biotech Co. Ltd (SHA: 688278) has announced plans to acquire partial assets of Skyline Therapeutics Limited, a clinical-stage gene therapy developer, excluding its U.S. subsidiary Skyline Therapeutics (US) Inc. The transaction includes a $15 million merger consideration plus up to $43 million in development, sales milestones, sub-license commissions,…
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Novo Nordisk’s Emerging Business Division VP Eve Jiang Departs for External Opportunities
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Jiang Yiwei (Eve Jiang), corporate vice president (CVP) of Novo Nordisk’s (NYSE: NVO) Emerging Business Division (EBD), is leaving the company to pursue external opportunities, with her last day set for March 3. Dr. Christine Zhou Xia Ping, Novo’s senior vice president and president of Region China, will assume the…
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Joyo Pharma’s JYP0015 Receives CDE Approval for RAS Mutation Cancer Trials
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China’s Center for Drug Evaluation (CDE) has tacitly approved Joyo Pharma’s Category 1 drug JYP0015, a molecular glue product, for clinical studies in hematological and solid tumors with RAS mutations. The approval follows positive preclinical data and a strategic licensing deal with U.S.-based Erasca, Inc. Drug ProfileJYP0015, a novel pan-RAS…
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Zhejiang Huahai Pharma’s HB0056 Receives NMPA Approval for Asthma Trials
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China-based Zhejiang Huahai Pharmaceutical Co., Ltd (SHA: 600521) announced that its bispecific antibody HB0056 has received clinical trial approval from China’s National Medical Products Administration (NMPA) for asthma. The approval follows similar clearances in New Zealand (October 2024) and the U.S. (January 2025), positioning the drug for global development. Clinical…
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Zhejiang Dian Diagnostics Partners with Best Covered to Tackle Alzheimer’s Disease
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Zhejiang Dian Diagnostics Co., Ltd (SHE: 300244), a China-based medical diagnostics firm, has formed a strategic partnership with Shanghai-based Best Covered, a technology company specializing in Alzheimer’s disease (AD). The collaboration aims to enhance early screening, precise testing, personalized intervention, and digital management of AD. Partnership GoalsThe two companies will…
