重药控股(000950.SZ)公告称,公司控股子公司重药股份收到国家药监局签发的《药物临床试验批准通知书》,同意开展盐酸普拉格雷片的临床试验。盐酸普拉格雷片原研公司为第一三共株式会社,是第三代的抑制ADP激活的血小板聚集的药物,适应于预防接受经皮冠状动脉介入治疗后的急性冠状动脉综合征、稳定型心绞痛、陈旧性心肌梗塞患者的血栓形成。目前已在全球70多个国家和地区上市(中国境内未上市)。
重药控股(000950.SZ)公告称,公司控股子公司重药股份收到国家药监局签发的《药物临床试验批准通知书》,同意开展盐酸普拉格雷片的临床试验。盐酸普拉格雷片原研公司为第一三共株式会社,是第三代的抑制ADP激活的血小板聚集的药物,适应于预防接受经皮冠状动脉介入治疗后的急性冠状动脉综合征、稳定型心绞痛、陈旧性心肌梗塞患者的血栓形成。目前已在全球70多个国家和地区上市(中国境内未上市)。
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