申请人:Jina Pharmaceuticals, Inc.
公开号:US11291640B2
公开(公告)日:2022-04-05
A method for maintaining a therapeutically effective concentration of endoxifen for the treatment of patient with bipolar I disorder is provided. The method includes administering to the patient a dose of 2 mg to 16 mg of endoxifen citrate in an enteric coated tablet once per day for at least 21 days. Further, the said method provides a desirable in-vivo plasma profile. The therapeutic dose monitoring is not required in a patient undergoing the said treatment. Furthermore, the method provides a significant improvement in mania assessed by the YMRS and the MADRS scores in patient undergoing the said treatment. Furthermore, the method as provides an early response time of the treatment in at least 2 days and remission time that is not more than 4 days in patient undergoing the said treatment.
本研究提供了一种维持内昔芬治疗有效浓度的方法,用于治疗双相情感障碍 I 患者。该方法包括给患者服用剂量为 2 毫克至 16 毫克枸橼酸内酯的肠溶片,每天一次,持续至少 21 天。此外,所述方法还提供了理想的体内血浆谱。接受上述治疗的患者无需进行治疗剂量监测。此外,该方法还能显著改善接受上述治疗的患者通过 YMRS 和 MADRS 评分评估的躁狂症。此外,该方法还能为接受上述治疗的患者提供至少 2 天的早期治疗反应时间和不超过 4 天的缓解时间。