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Yuekang Pharmaceutical: Subsidiary YKYY018's clinical approval for indications of inhalation aerosol therapy for the treatment and prevention of human parainfluenza virus infection
Recently, Yuekang Pharmaceutical issued an announcement stating that its wholly owned subsidiary, Beijing Yuekang Kerui Medical Technology Co., Ltd., has received a Notice of Approval for a drug clinical trial for its YKYY018 nebulized inhalation solution, approving the product to conduct clinical trials for the prevention and treatment of human parainfluenza virus infection.
YKYY018 nebulized inhalation solution is an internationally original fusion inhibition drug independently developed by the company based on its full-process AI platform. It has already received approval from the U.S. Food and Drug Administration and the National Medical Products Administration for clinical trials aimed at preventing and treating respiratory syncytial virus infection.
As of now, there are no approved drugs or vaccines for the treatment of human parainfluenza virus infection worldwide, and there is a significant and urgent unmet need in the fields of clinical treatment and prevention.
(Yuekang Pharmaceutical announcement)
(Editor: Yang Yan Lin Chen)
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