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Lumateperone的处方量(TRxs)
Lumateperone的处方量(TRxs)
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所属报告:
CNS创新药系列报告(四):新机制抗抑郁药快速改善症状有望重塑市场格局-241010(44页).pdf
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相关数据
Auvelity的处方量(TRxs)
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行业数据
2024-10-14
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美国精神分裂症、双相障碍和抑郁症患者人数及Lumateperone的市场空间
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行业数据
2024-10-14
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Lumateperone与部分第2代抗精神病药受体亲和性(Ki值)比较(nM)
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2024-10-14
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Lumateperone 已获批精神分裂症和双相障碍适应症。2019 年 12 月,美国 FDA 批准Lumateperone(42mg/日,商品名 Caplyta)用于成人精神分裂症的治疗。2021 年 12 月,美国 FDA批准 Lumateperone 新适应症:作为单药疗法、以及作为锂盐或丙戊酸盐的辅助疗法(范围最广),用于成人双相障碍 I 型或 II 型患者的抑郁发作,新适应症获批后总处方量(TRxs)迅速增加。2023年,Caplyta 实现销售额 4.62 亿美元(YoY+86%),2024 年公司指引为 6.45-6.75 亿美元。
行业数据
原图定位
当前图表所属:
CNS创新药系列报告(四):新机制抗抑郁药快速改善症状有望重塑市场格局-241010(44页).pdf
2024年抗抑郁药物行业报告:现有疗法缓解率仅67%,新机制快速起效
氨基酸类神经质靶点在研抗抑郁药物
一线抗抑郁药物常见不良反应发生率
抗抑郁药物导致的神经突触可塑性变化
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