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NCT05604287

Safety, Tolerability, and Pharmacokinetics of ID119031166M With the Exploration of Pharmacodynamic Effects

Terminated Phase 1 Last updated 11 July 2024
What this trial tests

Phase 1 trial testing ID119031166M in Healthy Participants in 67 participants. Terminated before completion.

Timeline
10 October 2022
Primary endpoint
12 April 2024
12 April 2024

Quick facts

Lead sponsorIlDong Pharmaceutical Co Ltd
PhasePhase 1
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designsequential
Maskingdouble
Primary purposetreatment
Enrollment67
Start date10 October 2022
Primary completion12 April 2024
Estimated completion12 April 2024
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

IlDong Pharmaceutical Co Ltd — full company profile →

Who can join

Adults 18 to 70, any sex, with Healthy Participants. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study will evaluate safety, tolerability, and Pharmacokinetics (PK) of ID119031166M with the Exploration of Pharmacodynamic (PD) effects in Healthy Participants.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Nuclear receptors in health and disease: signaling pathways, biological functions and pharmaceutical interventions.
    Jin P, Duan X, Huang Z, Dong Y, et al · · 2025 · cited 21× · PMID 40717128 · DOI 10.1038/s41392-025-02270-3

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Other recruiting trials for Healthy Participants

Currently open trials in the same condition.

Other IlDong Pharmaceutical Co Ltd trials

Trials by the same sponsor.

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Data sources for this page

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing