Category News

Cayuga Biotech Accelerates Life-Saving Hemorrhage Treatment with PolyP-SNP Complex, Promising 12x Faster Coagulation

Cayuga Biotech introduced groundbreaking preclinical findings today on its innovative polyphosphate (polyP)-based therapy aimed at combating life-threatening hemorrhage. The study revealed that the polyP-SNP (silica nanoparticle) complex accelerates thrombin production 12 times faster than conventional methods under both standard and…

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PQE Group Introduces AI and Data Analytics Division: Pioneering Innovations in Life Science

PQE Group, a prominent consultancy in the Life Science sector, has announced the launch of its new Regulated Artificial Intelligence & Data Analytics division. This development follows the integration of AI-based tools within the industrial sector, marking a significant milestone…

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EU Approves Takeda’s FRUZAQLA for Treated Metastatic Colorectal Cancer

Takeda has announced that the European Commission (EC) has approved FRUZAQLA (fruquintinib) as a monotherapy for adult patients with metastatic colorectal cancer (mCRC) who have previously been treated with standard therapies. These therapies include fluoropyrimidine-, oxaliplatin-, and irinotecan-based chemotherapies, anti-VEGF…

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ISTH: Sanofi Strengthens Hemophilia Leadership with New Data on ALTUVIIIO and Fitusiran

Sanofi is set to present new data from its hemophilia portfolio at the 32nd Congress of the International Society on Thrombosis and Haemostasis (ISTH), occurring from June 22-26, 2024, in Bangkok, Thailand. Key presentations on ALTUVIIIO [Antihemophilic Factor (Recombinant), Fc-VWF-XTEN…

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Takeda Reports Phase 3 Findings of Soticlestat (TAK-935) in Patients with Dravet Syndrome and Lennox-Gastaut Syndrome

Takeda Releases Phase 3 Topline Results for Soticlestat (TAK-935) in Dravet Syndrome and Lennox-Gastaut Syndrome OSAKA, Japan & CAMBRIDGE, Mass.–(BUSINESS WIRE)–Takeda (TSE:4502/NYSE The SKYLINE trial (TAK-935-3001) was a multicenter, randomized, double-blind Phase 3 study examining soticlestat (TAK-935) alongside standard care…

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Celltrion Unveils Promising Phase III Results for CT-P47, a Biosimilar to RoActemra®, in RA Patients at EULAR 2024

Celltrion today presented positive Phase III data for CT-P47, a biosimilar referencing RoActemra® in patients with moderate-to-severe rheumatoid arthritis (RA), at the Annual European Congress of Rheumatology (EULAR) 2024. The trial demonstrated that CT-P47 has equivalent efficacy and comparable safety…

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Zimbabwe Achieves WHO Maturity Level 3 in Medicine Regulation, Joining Africa’s Elite Six

Zimbabwe has reached maturity level 3 (ML 3) in the WHO’s classification of regulatory authorities for medicines, marking a significant achievement in healthcare infrastructure. This classification, assessed using WHO’s Global Benchmarking Tool with over 260 indicators, signifies the establishment of…

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