KCT0006614终止未知
A Double-blind, Multi-center, Multi-regional, Randomized Controlled, Phase 3 Clinical Trial to Evaluate the Efficacy and Safety of CKD-314 in Hospitalized Adult Patients Diagnosed with COVID-19
Chong Kun Dang0 个研究点目标入组 586 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 终止
- 发起方
- 入组人数
- 586
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional Study
入排标准
- 年龄范围
- 18(Year) 至 o Limit（—）
- 性别
- All
入选标准
- •1) Patients aged = 18 years
- •2) Patients diagnosed with COVID-19 infection and pneumonia
- •3) Patients who have voluntarily decided to participate in the study and signed the informed consent form
排除标准
- •1) Patients with history of hypersensitivity to the study drug
- •2) Female patients, either who are or may be pregnant or who are breastfeeding, or female patients of child-bearing potential who are unable to use adequate contraception during the study
- •3) Patients who are deemed to ineligible to participate in the study for other reasons by the investigator
研究者
相似试验
Unknown
3 期
Phase 3 Clinical Trial to Evaluate the Efficacy and Safety of CKD-314CTRI/2021/12/038691Chong Kun Dang Pharmaceutical Corp46
招募中
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进行中（未招募）
不适用
An International, Multicenter, Double-blind, Randomized, Placebo-controlled, Phase IV Study of the Safety and Efficacy of Lithium versus Placebo as an add on to SEROQUEL XR™ (Quetiapine Fumarate) in Adult Patients with Acute ManiaAcut mania in subjects with bipolar I disorderMedDRA version: 9.1Level: PTClassification code 10004939Term: Bipolar I disorderEUCTR2008-007190-20-DEAstraZeneca AB350