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Cybin Inc., a clinical-stage biopharmaceutical company, has reported positive Phase 2 topline results for its CYB003 program in treating Major Depressive Disorder (MDD), with 79% of patients achieving remission after two doses. The company plans to advance to a Phase 3 trial in early 2024. Cybin's robust intellectual property portfolio includes 40 granted patents and over 170 pending applications. The company also highlighted its upcoming milestones, including additional Phase 2 data, an FDA end-of-Phase 2 meeting, and the initiation of a Phase 2 study of deuterated dimethyltryptamine (dDMT) for Generalized Anxiety Disorder (GAD) in early 2024. Cybin's CEO, Doug Drysdale, expressed confidence in the potential of their clinical programs to revolutionize mental health treatment. The company's DMT program, including CYB004 and SPL028, has completed multiple clinical trials, with Phase 1 topline data expected early in the first quarter of 2024. Cybin aims to initiate a Phase 2 GAD study within the same quarter.
Cybin Inc., a clinical-stage biopharmaceutical company, has reported positive Phase 2 topline results for its CYB003 program in treating Major Depressive Disorder (MDD), with 79% of patients achieving remission after two doses. The company plans to advance to a Phase 3 trial in early 2024. Cybin's robust intellectual property portfolio includes 40 granted patents and over 170 pending applications. The company also highlighted its upcoming milestones, including additional Phase 2 data, an FDA end-of-Phase 2 meeting, and the initiation of a Phase 2 study of deuterated dimethyltryptamine (dDMT) for Generalized Anxiety Disorder (GAD) in early 2024. Cybin's CEO, Doug Drysdale, expressed confidence in the potential of their clinical programs to revolutionize mental health treatment. The company's DMT program, including CYB004 and SPL028, has completed multiple clinical trials, with Phase 1 topline data expected early in the first quarter of 2024. Cybin aims to initiate a Phase 2 GAD study within the same quarter.
临床阶段的生物制药公司Cybin Inc. 报告了其治疗重度抑郁症（MDD）的 CYB003 项目的 2 期临床表现良好，79% 的患者在接种两剂后获得缓解。该公司计划在2024年初推进第三阶段试验。Cybin强大的知识产权组合包括40项已获授权的专利和170多项待处理的申请。该公司还强调了其即将到来的里程碑，包括额外的2期数据、FDA的第二阶段末会议以及2024年初启动的治疗广泛性焦虑症（GAD）的氘化二甲基色胺（ddMT）的2期研究。Cybin的首席执行官道格·德赖斯代尔对他们的临床项目有可能彻底改变心理健康治疗表示信心。该公司的DMT项目，包括 CYB004 和 SPL028，已经完成了多项临床试验，第一阶段的主要数据预计将在2024年第一季度初发布。Cybin的目标是在同一季度内启动一项第二阶段的GAD研究。
临床阶段的生物制药公司Cybin Inc. 报告了其治疗重度抑郁症（MDD）的 CYB003 项目的 2 期临床表现良好，79% 的患者在接种两剂后获得缓解。该公司计划在2024年初推进第三阶段试验。Cybin强大的知识产权组合包括40项已获授权的专利和170多项待处理的申请。该公司还强调了其即将到来的里程碑，包括额外的2期数据、FDA的第二阶段末会议以及2024年初启动的治疗广泛性焦虑症（GAD）的氘化二甲基色胺（ddMT）的2期研究。Cybin的首席执行官道格·德赖斯代尔对他们的临床项目有可能彻底改变心理健康治疗表示信心。该公司的DMT项目，包括 CYB004 和 SPL028，已经完成了多项临床试验，第一阶段的主要数据预计将在2024年第一季度初发布。Cybin的目标是在同一季度内启动一项第二阶段的GAD研究。
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