NL-OMON55052已完成2 期
A multicentre study to assess safety and efficacy of COMP360 in patients with treatment-resistant depression following completion of COMP 001 and COMP 003 trials (P-TRD LTFU) - COMP360 in Participants with Treatment Resistant Depression
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 3
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •1)Signed ICF
- •2)Each participant having completed the final study visit of either COMP 001 or
- •3)Ability to complete all protocol required assessment tools (including having
- •access to the internet in order to complete the digital assessments) without
- •any assistance or alteration to the copyrighted assessments, and to comply with
- •all study visits
排除标准
- •1)Subject has any condition, for which in the opinion of the investigator,
- •participation would not be in the interest of the subject eg participation
- •could compromise the wellbeing of the participant or prevent, limit, or
- •confound the protocol-specified assessments
研究者
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ong Term Follow up study for subjects that participated in COMP001 and COMP003 trialTreatment-Resistant Depression (P-TRD)MedDRA version: 21.1Level: LLTClassification code 10025463Term: Major depressive disorder, single episodeSystem Organ Class: 100000004873MedDRA version: 21.1Level: LLTClassification code 10025454Term: Major depressive disorder, recurrent episodeSystem Organ Class: 100000004873EUCTR2020-001348-25-DKCOMPASS Pathfinder, Ltd150