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A Study to Evaluate the Efficacy and Safety of AD-224

A

Addpharma

Status and phase

Enrolling
Phase 3

Conditions

Hypertension,Essential

Treatments

Drug: Placebo of AD-224A
Drug: AD-224B
Drug: AD-224C
Drug: AD-224A
Drug: Placebo of AD-224C
Drug: Placebo of AD-224B

Study type

Interventional

Funder types

Industry

Identifiers

NCT06291207
AD-224P3

Details and patient eligibility

About

The purpose of this study is to evaluate the efficacy and safety of AD-224

Full description

Condition or disease : Essential Hypertension

Enrollment

252 estimated patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Signed informed consent
  • Patients with Essential Hypertension
  • Other inclusions applied

Exclusion criteria

  • Patient with Secondary Hypertension
  • Other exclusions applied

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

252 participants in 3 patient groups

AD-224A
Experimental group
Description:
AD-224A+Placebo of AD-224B+Placebo of AD-224C
Treatment:
Drug: Placebo of AD-224B
Drug: Placebo of AD-224C
Drug: AD-224A
AD-224B
Experimental group
Description:
Placebo of AD-224A+AD-224B+Placebo of AD-224C
Treatment:
Drug: Placebo of AD-224C
Drug: AD-224B
Drug: Placebo of AD-224A
AD-224C
Active Comparator group
Description:
Placebo of AD-224A+Placebo of AD-224B+AD-224C
Treatment:
Drug: Placebo of AD-224B
Drug: AD-224C
Drug: Placebo of AD-224A

Trial contacts and locations

1

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Central trial contact

JeongEun Park

Data sourced from clinicaltrials.gov

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