China-based LakeShore Biopharma Co Ltd (Nasdaq:LSB) announced on Wednesday that it has held the 2025 CSO (Contract Sales Organisation) Annual Meeting and the launch meeting of YSJA rabies vaccine (Vero cell) novel packaging solution (liquid drug transfer device) in Changsha, Hunan Province.
Approved for lot release by regulatory authorities on 15 April 2025, the new formulation will begin nationwide distribution in China within weeks.
The company says that to address pain points such as compounding contamination, occupational exposure of medical staff and needle tip pain, the novel packaging YSJA vaccine has been upgraded accordingly. The novel packaging product is equipped with specially designed clasp, puncture device and suction head, which can realise automatic clamping, needle-free reconstitution and new needle injection, improve the convenience and safety of vaccination, reduce the risk of particle pollution and inflammation, and protect medical staff from needlestick injuries.
"The YSJA packaging innovation represents humanised design in vaccine delivery," said Wang Xu, LakeShore Biopharma CEO. "By leveraging closed sterile connection technology, this novel design will gradually address the industry pain points of 'occupational exposure and pollution risk' in the traditional liquid preparation process. This launch marks the first commercial application of such advanced liquid transfer device in China's rabies vaccine market, filling a significant unmet need."
TNF Pharmaceuticals showcases isomyosamine's clinical promise at BGS Spring Meeting 2025
Hoth Therapeutics reports positive initial data from Phase 2a pruritus trial
Galmed reveals novel pharmacodynamic blood markers for Aramchol SCD1 inhibitor
Evommune initiates EVO756 Phase 2b trial in adults with chronic spontaneous urticaria
Sanofi advances respiratory pipeline with positive amlitelimab data and expanded clinical programmes
Halozyme Therapeutics' VYVGART Hytrulo prefilled syringe for self-injection receives US FDA approval
Alphyn doses first patient in Phase 2b trial of Zabalafin Hydrogel in Australia
Ananda Pharma's MRX1 receives ethics approval for Phase 1 study in Australia
Organon acquires US rights to TOFIDENCE from Biogen
Dupixent receives approval in Japan as first biologic for COPD treatment
Celltrion adds STEQEYMA to Costco Member Prescription Program
Alys Pharmaceuticals doses first patient in Phase IIa trial of ALY-101
Bio-Thera Solutions signs commercialisation and licence agreements with Dr. Reddy's Laboratories
Spyre Therapeutics starts dosing in Phase 1 clinical trial of SPY003
Vast Therapeutics' ALX1 drug candidate granted QIDP designation by US FDA