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NCT05833906

Safety, Tolerability, and Pharmacokinetic Evaluations of CKR-051 After Transdermal Administration in Healthy Male Subjects

Completed Phase 1 Last updated 19 January 2024
What this trial tests

Phase 1 trial testing CKR-051 Dose 1 in Healthy in 52 participants. Completed in 8 January 2024.

Timeline
25 April 2023
Primary endpoint
8 January 2024
8 January 2024

Quick facts

Lead sponsorCK Regeon Inc.
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposescreening
Enrollment52
Start date25 April 2023
Primary completion8 January 2024
Estimated completion8 January 2024
Sites1 location across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

CK Regeon Inc. — full company profile →

Who can join

Adults 19 to 60, male only, with Healthy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study will evaluate the safety, tolerability, and pharmacokinetics (PK) of CKR-051 in healthy participants. This study aiming to develop an agent for skin regeneration; potential treatments include acute and chronic wounds (c.f. Diabetic foot ulcers).

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05833906.

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