A Study to Evaluate the Efficacy and Safety of AD-221 and AD-221A

  • STATUS
    Recruiting
  • participants needed
    240
  • sponsor
    Addpharma Inc.
Updated on 24 November 2021

Summary

The purpose of this study is to evaluate the efficacy and safety of AD-221 and AD-221A

Description

The purpose of this study is to evaluate the efficacy and safety of AD-221 and AD-221A in patients with primary hypercholesterolemia

Details
Condition Primary Hypercholesterolemia
Age 19years or above
Treatment AD-221, AD-221A, AD-221B, AD-221C
Clinical Study IdentifierNCT05131997
SponsorAddpharma Inc.
Last Modified on24 November 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Signed informed consent
Subjects with primary hypercholesterolemia

Exclusion Criteria

Patient with secondary dyslipidemia
Other exclusions applied
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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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