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Esco Aster and Shine-On Biomedical secured FDA approval for a first-in-class exosome drug, now in Phase I trials.
Esco Aster, a Singapore-based CRDMO, has secured a clinical cGMP manufacturing agreement with Shine-On Biomedical to advance a first-in-class exosome drug platform targeting HLA-G.
The collaboration, active since 2023, supported Shine-On’s successful U.S. FDA IND approval in early 2025 for its lead candidate, SOB100, now in Phase I trials.
The platform shows promise in delivering therapeutic molecules, with positive preclinical biodistribution results.
Esco Aster’s 3D Tide Motion™ bioreactor enables efficient exosome production, and the company continues exploratory loading studies.
The partnership also supports autologous cell therapy programs across ASEAN and broader biomanufacturing efforts in the Asia-Pacific region.
Esco Aster y Shine-On Biomedical aseguraron la aprobación de la FDA para un fármaco exosómico de primera clase, ahora en ensayos de Fase I.