Phase 3 Clinical Trial to Evaluate the Efficacy and Safety of CKD-314

  • days left to enroll
  • participants needed
  • sponsor
    Chong Kun Dang Pharmaceutical
Updated on 14 August 2021


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


To evaluate the efficacy and safety of CKD-314 by comparing the study group and control group in hospitalized adult patients diagnosed with COVID-19 pneumonia

Condition COVID 19 Pneumonia
Treatment CKD-314+SOC, CKD-314 Placebo+SOC
Clinical Study IdentifierNCT04871646
SponsorChong Kun Dang Pharmaceutical
Last Modified on14 August 2021


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Inclusion Criteria

Patients aged 18 years
Patients diagnosed with COVID-19 infection and pneumonia
Patients who have voluntarily decided to participate in the study and signed the informed consent form If a patient cannot provide consent on his or her own, informed consent by a legally authorized representative may be obtained

Exclusion Criteria

Patients with history of hypersensitivity to the study drug
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
Patients who are deemed to ineligible to participate in the study for other reasons by the investigator
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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