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9月9日，中国国家药监局药品审评中心（CDE）官网公示，中国生物制药研发的1类新药TQC3721吸入粉雾剂获批临床，拟开发用于慢性阻塞性肺疾病（COPD）的维持治疗。TQC3721是中国研发进度最快的国产PDE3/4双重抑制剂。目前，吸入混悬液剂型正在中国开展治疗中重度COPD的II期临床研究，本次为吸入粉雾剂剂型首次在中国获批临床。

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With more than 300 patients in the trial, dubbed FOREMOST, 33.9% of those assigned to apremilast achieved minimal disease ...

By Dr. Priyom Bose, Ph.D. New study links higher antioxidant intake to reduced erectile dysfunction risk, highlighting the ...

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