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BioCina began manufacturing a reformulated injectable quetiapine for delirium treatment, supporting 2026 human trials under FDA’s 505(b)(2) pathway.
BioCina has launched a Chemistry, Manufacturing, and Controls (CMC) program for RLS-2201, a reformulated injectable quetiapine being developed by Patrys Ltd to treat delirium in intensive care.
Manufactured at BioCina’s Perth facility using a closed isolator system, the sterile product will support stability testing and supply early clinical materials.
First-in-human trials are expected in the second half of 2026, marking a key step toward regulatory approval under the FDA’s 505(b)(2) pathway.
The collaboration aims to de-risk development and establish a compliant manufacturing process.
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BioCina comenzó a fabricar una quetiapina inyectable reformulada para el tratamiento del delirio, apoyando 2026 ensayos en humanos bajo la vía 505 (b) (2) de la FDA.