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NCT07312799Not yet recruitingPhase 1

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

A Two-arm, Open-label, Single-sequence, Multiple-dose Study to Evaluate the Pharmacokinetic Interaction and the Safety of AD-2321 and AD-2322 in Healthy Adult Volunteers

Source: ClinicalTrials.gov · Last updated 31 Dec 2025

Brief summary (registry, in English)

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

Status (registry)
Not yet recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
41 (estimated)
First submitted
17 Dec 2025
Start date
27 Jan 2026
Primary completion date
11 Feb 2026
Lead sponsor
Addpharma Inc.
NCT number
NCT07312799

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 41
  • From 27 Jan 2026 to the primary completion date, 11 Feb 2026
  • 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.

Prior treatment

  • Participation in another clinical study with an investigational drug within the 6 months from scheduled first administration

Other

  • Other exclusions applied

Who the study is looking for

  • 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

Age in the registry: 19 years to 64 years · Sex: All · Accepts 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
H+ Yangji Hospital
Coordinator of this site? Confirm its status
SeoulSouth KoreaUnknown status

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