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A Study to Evaluate the Pharmacokinetic Interaction and the Safety of AD-236A and AD-236B

NCT07730567 · Status: NOT_YET_RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 44

Last updated 2026-07-28

No results posted yet for this study

Summary

To evaluate the pharmacokinetic interaction and the safety of AD-236A and AD-236B in healthy adult volunteers

Conditions

Interventions

DRUG

Treatment A(AD-236A)

AD-236A Oral Tablet

DRUG

Treatment B(AD-236B)

AD-236B Oral Tablet

DRUG

Treatment C(AD-236A+AD-236B)

AD-236A+AD-236B Oral Tablet

Sponsors & Collaborators

  • Addpharma Inc.

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
19 Years
Max Age
55 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-07-29
Primary Completion
2026-09-13
Completion
2026-09-26

Countries

  • South Korea

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07730567 on ClinicalTrials.gov