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Trials / Recruiting

RecruitingNCT07433556

Safety, Tolerability, Pharmacokinetic and Pharmacodynamic of IY-828026 in Healthy Volunteers

A Randomized, Double-blinded, Partial-open, Placebo/Active-controlled, Single/Multiple Dosing, Dose Escalation Phase 1 Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Characteristics of IY-828026 in Healthy Adult Volunteers

Status
Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
86 (estimated)
Sponsor
Il-Yang Pharm. Co., Ltd. · Industry
Sex
All
Age
19 Years – 50 Years
Healthy volunteers
Accepted

Summary

A randomized, double-blinded, partial-open, placebo/active-controlled, single/multiple dosing, dose escalation phase 1 clinical trial to evaluate the safety, tolerability, pharmacokinetic, and pharmacodynamic characteristics of IY-828026 in healthy adult volunteers

Conditions

Interventions

TypeNameDescription
DRUGIY-828026IY-828026
DRUGPlaceboPlacebo comparator
DRUGIY-828026AActive comparator
DRUGIY-828026BActive comparator

Timeline

Start date
2026-03-23
Primary completion
2027-03-01
Completion
2027-06-01
First posted
2026-02-25
Last updated
2026-03-27

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT07433556. Inclusion in this directory is not an endorsement.

Safety, Tolerability, Pharmacokinetic and Pharmacodynamic of IY-828026 in Healthy Volunteers (NCT07433556) · Clinical Trials Directory