【财华社讯】长风药业(02652.HK)公布,ICF004吸入粉雾剂的I类新药临床试验("IND")申请近期已获得中国国家药品监督管理局("NMPA")批准。该产品拟用于治疗间质性肺病(ILD),包括但不限于特发性肺纤维化(IPF)及进行性肺纤维化(PPF)。
特别声明:以上内容(如有图片或视频亦包括在内)为自媒体平台“网易号”用户上传并发布,本平台仅提供信息存储服务。
Notice: The content above (including the pictures and videos if any) is uploaded and posted by a user of NetEase Hao, which is a social media platform and only provides information storage services.