3PBIOVIAN and the Colombia INC has signed a contract to carry out the development of a biosimilar monoclonal antibody (mAb) for an oncology indication, marking the first biosimilar mAb to be developed...
Read moreEstos microcompartimentos pueden encapsular ADN o ARN y fusionarse con la membrana celular de forma natural, liberando su contenido con una eficiencia sorprendentemente alta y una toxicidad mucho meno...
Read moreMientras que los ELISAs clásicos requieren múltiples fases de incubación, lavados y preparación manual de reactivos, los Instant ELISA de Abylabel están diseñados para ofrecer resultados en meno...
Read moreThe European Medicines Agency (EMA) has designated as an orphan drug a compound based on the bioactive lipid molecule Maresin-1 (MaR1), currently being investigated by a research team from the UAB for...
Read moreAptadel Therapeutics takes another step forward in the development of its treatment for Ewing’s sarcoma. The biotechnology company has closed a bridge round of 2 million euros with the entry o...
Read moreMTBVAC is based directly on Mycobacterium tuberculosis, the human pathogen, whereas BCG is derived from Mycobacterium bovis. This means that MTBVAC retains key antigens present in the original pathoge...
Read moreThe modern drug development timeline is highly shaped by manufacturing readiness, analytical understanding, and regulatory alignment. While innovation in therapeutic modalities has accelerated target ...
Read moreBiotechnology company 53Biologics, specialized in the development and manufacturing of biologic drugs, has announced the closing of a strategic funding round led by European private equity firm Ren Li...
Read moreLa Agencia Estadounidense de Alimentos y Medicamentosha aprobado el medicamento de terapia génica denominado KRESLADI™ (marnetegragene autotemcel) de la empresa Rocket Pharma para el tratamiento de...
Read moreMost biotech teams assume GMP readiness begins when a product enters clinical phases. In reality, the foundations of GMP are built much earlier, during drug development, often without being explicitly...
Read moreSponsored by F. Hoffmann-La Roche Ltd, in collaboration with Vall d’Hebron Institute of Oncology (VHIO), a first-in-human clinical trial was designed to assess the safety, maximum tolerated dose, an...
Read moreGTX-11, developed by GAT Therapeutics and protected by patent, is a small oral molecule that modulates the TGFβ signalling pathway, a key factor in fibrotic processes, characterised by the excessive ...
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