drugset / Trial / NCT05833906

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

NCT05833906 ↗

Phase 1 Completed 52 enrolled CK Regeon Inc.
RandomizedParallel-groupSingle-blindScreening

Summary

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).

Timeline

Start
2023-04-25
Primary completion
2024-01-08
Completion
2024-01-08

Drugs

EvaluationDrugModalityDoseRoute
Subject CKR-051 Unknown 5 g Other
Subject CKR-051 Unknown 10 g Other

Indications

No indication recorded.