Study to Evaluate the Efficacy and Safety in Patients With Primary Hypercholesterolemia

  • STATUS
    Recruiting
  • days left to enroll
    76
  • participants needed
    264
  • sponsor
    Ahn-Gook Pharmaceuticals Co.,Ltd
Updated on 23 March 2022

Summary

To Evaluate the Efficacy and Safety of Combination Therapy of AGT and AGZ Versus Monotherapy of AGT in Patients With Primary Hypercholesterolemia.

Description

A Multi-center, Randomized, Double-blinded, Active-controlled, Factorial Design Phase 3 Clinical Trial

Details
Condition Primary Hypercholesterolemia
Treatment AGT2, AGZ, AGT2, AGT4, AGZ, AGT4
Clinical Study IdentifierNCT05206578
SponsorAhn-Gook Pharmaceuticals Co.,Ltd
Last Modified on23 March 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Patients with primary hypercholesterolemia

Exclusion Criteria

The subject not meet the specified LDL-C level
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  • You can expect the study team to contact you via email or phone in the next few days.
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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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