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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05631990
Other study ID # AD-209P2-02
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date April 5, 2023
Est. completion date November 27, 2023

Study information

Verified date April 2024
Source Addpharma Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the efficacy and safety of AD-209


Description:

Condition or disease : hypertension Intervention/treatment Drug : AD-209 Drug : AD-209-1A Drug : AD-209-1B Drug : AD-209-1C Drug : AD-209 Placebo Drug : AD-209-1 Placebo Phase : Phase 2


Recruitment information / eligibility

Status Completed
Enrollment 221
Est. completion date November 27, 2023
Est. primary completion date November 27, 2023
Accepts healthy volunteers No
Gender All
Age group 19 Years to 74 Years
Eligibility Inclusion Criteria: - Signed informed consent - Other inclusions applied Exclusion Criteria: - orthostatic hypotension with symptom - Other exclusions applied

Study Design


Intervention

Drug:
AD-209
PO, Once daily(QD), 8weeks
AD-209-1A
PO, Once daily(QD), 8weeks
AD-209-1B
PO, Once daily(QD), 8weeks
AD-209-1C
PO, Once daily(QD), 8weeks
AD-209 placebo
PO, Once daily(QD), 8weeks
AD-209-1 placebo
PO, Once daily(QD), 8weeks

Locations

Country Name City State
Korea, Republic of Korea University Guro Hospital Seoul

Sponsors (1)

Lead Sponsor Collaborator
Addpharma Inc.

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change rate of MSSBP Change from baseline in mean sitting systolic blood pressure Baseline, Week 8
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