Clinical Trial to Evaluate the Efficacy and Safety of D064 and D702 Combination Therapy

Last updated: June 2, 2024
Sponsor: Chong Kun Dang Pharmaceutical
Overall Status: Completed

Phase

3

Condition

Diabetes And Hypertension

High Blood Pressure (Hypertension - Pediatric)

Vascular Diseases

Treatment

D660, placebo of D064, placebo of D702

D064, D702, placebo of D660

Clinical Study ID

NCT05931224
A30_15HT2213
  • Ages > 19
  • All Genders

Study Summary

Clinical Trial to Evaluate the Efficacy and Safety of D064 and D702 Combination Therapy

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Subjects who are 19 years old or older.

  • Subjects who have voluntarily decided to participate in this clinical trial andsigned ICF.

Exclusion

Exclusion Criteria:

  1. Subjects with a history of secondary hypertension or suspected secondaryhypertension

  2. Subjects with hypersensitivity or history of clinical trial drugs and similar drugs

  3. Subjects who are required to administer a combination of prohibited drugs specifiedin this plan during the clinical trial participation period

  4. Subjects with a history of drug or alcohol abuse or suspected patient within 24weeks as of the time of screening

  5. Subjects who received other clinical trial drugs within 4 weeks of screening visit.

  6. Pregnant women, lactating women, or Subjects who do not agree to use appropriatecontraception during the clinical trial period and for two weeks after the end ofadministration of the last clinical trial drug

  7. Subjects who are unable to participate in this clinical trial at the discretion ofthe investigator.

Study Design

Total Participants: 346
Treatment Group(s): 2
Primary Treatment: D660, placebo of D064, placebo of D702
Phase: 3
Study Start date:
June 28, 2023
Estimated Completion Date:
May 13, 2024

Connect with a study center

  • Seoul National University Bundang Hospital

    Seongnam, Bundang-gu 13620
    Korea, Republic of

    Site Not Available

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