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NCT06416865CompletedPhase 3

Efficacy and Safety of AJU-C52 in Essential Hypertension Patients

A Randomized, Double-blind, Multi-center, Phase III Trial to Evaluate the Efficacy and Safety of AJU-C52 in Compared With C52R1M for Essential Hypertension Patients in Inappropriately Controlled on C52R1L Treatment

Source: ClinicalTrials.gov · Last updated 21 Sept 2026

Brief summary (registry, in English)

A Randomized, Double-blind, Multi-center, Phase III study to evaluate the efficacy and safety of the AJU-C52 compared with the combination of C52R1M in patients with essential Hypertension Patients who have inappropriately controlled on C52R1L treament

Status (registry)
Completed
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
193 (actual)
First submitted
12 May 2024
Start date
18 Oct 2022
Primary completion date
23 Dec 2024
Lead sponsor
AJU Pharm Co., Ltd.
NCT number
NCT06416865

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 193
  • From 18 Oct 2022 to the primary completion date, 23 Dec 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Secondary hypertension patients or those with a history of suspected secondary hypertension
  • Cardiovascular/cerebrovascular disease
  • Those with a history of malignant tumor within 5 years

Other

  • At the screening visit (Visit 1), patients had 3 blood pressure measurements in the arm with the higher average MSSBP, those whose maximum and minimum blood pressure differences are MSSBP 20 mmHg and MSDBP 10 mmHg

Who the study is looking for

  • Adults aged ≤19 years.
  • Those who voluntarily signed the informed consent to participate in this study.
  • A patient diagnosed with essential hypertension or Patients taking hypertension medication
  • Those who are eligible for adequate blood pressure criteria during screening tests: Naïve patient-160 mmHg≤MSSBP\<200 mmHg and MSDBP\<110 mmHg/Patients taking hypertension medication-140 mmHg≤MSSBP\<200 mmHg and MSDBP\<110 mmHg

Age in the registry: 19 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
AJU Pharm Co., Ltd.
Coordinator of this site? Confirm its status
SeoulSouth KoreaUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.