MedDataX Logo

Evaluate the Pharmacokinetic Interaction and the Safety of AD-2321 and AD-2322

NCT ID: NCT07312799

Last Updated: 2025-12-31

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

PHASE1

Total Enrollment

41 participants

Study Classification

INTERVENTIONAL

Study Start Date

2026-01-27

Study Completion Date

2026-02-26

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

To evaluate the pharmacokinetic interactions of AD-2321, AD-2322 in healthy adult volunteers.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Hypertension

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Arm A

Period 1 : Treatment A(AD-2321), Period 2 : Treatment C(AD-2321+AD-2322)

Group Type EXPERIMENTAL

Treatment A(AD-2321)

Intervention Type DRUG

AD-2321 Oral Tablet

Treatment C(AD-2321+AD-2322)

Intervention Type DRUG

AD-2321 Oral Tablet+AD-2322 Oral Tablet

Arm B

Period 1 : Treatment B(AD-2322), Period 2 : Treatment C(AD-2321+AD-2322)

Group Type EXPERIMENTAL

Treatment B(AD-2322)

Intervention Type DRUG

AD-2322 Oral Tablet

Treatment C(AD-2321+AD-2322)

Intervention Type DRUG

AD-2321 Oral Tablet+AD-2322 Oral Tablet

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Treatment A(AD-2321)

AD-2321 Oral Tablet

Intervention Type DRUG

Treatment B(AD-2322)

AD-2322 Oral Tablet

Intervention Type DRUG

Treatment C(AD-2321+AD-2322)

AD-2321 Oral Tablet+AD-2322 Oral Tablet

Intervention Type DRUG

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Healthy adult volunteers aged ≥19 and \<65 years at the time of the screening visit
* Body weight ≥50 kg (≥45 kg for females) and body mass index (BMI) between 18.0 kg/m² and 30.0 kg/m² at the time of the screening visit

Exclusion Criteria

* Participation in another clinical study with an investigational drug within the 6 months from scheduled first administration
* Other exclusions applied
Minimum Eligible Age

19 Years

Maximum Eligible Age

64 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Addpharma Inc.

INDUSTRY

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

H+ Yangji Hospital

Seoul, , South Korea

Site Status

Countries

Review the countries where the study has at least one active or historical site.

South Korea

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

SoonKeun Kwon

Role: CONTACT

Phone: +82318916915

Email: [email protected]

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

SeungHyun Kang

Role: primary

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

AD-232DDI

Identifier Type: -

Identifier Source: org_study_id