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drugset / Trial / NCT05701644

Study To Evaluate the Safety, Tolerability, and Pharmacokinetics After Subcutaneous Administration of C1K in Healthy Subjects

NCT05701644 ↗

Phase 1 Completed 36 enrolled Ensol Bioscience
RandomizedParallel-groupTriple-blindTreatment

Summary

A dose-block randomized, double-blind, placebo-controlled, single and multiple ascending dose, first-in-human, phase 1 first in human clinical trial to evaluate the safety, tolerability, and pharmacokinetics after subcutaneous administration of C1K in healthy Korean subjects.

Timeline

Start
2023-01-02
Primary completion
2023-06-28
Completion
2023-06-28

Drugs

EvaluationDrugModalityDoseRoute
Subject C1K Unknown 150 mg Subcutaneous
Subject C1K Unknown 300 mg Subcutaneous
Subject C1K Unknown 600 mg Subcutaneous
Subject C1K Unknown 900 mg Subcutaneous
Subject C1K Unknown 1200 mg Subcutaneous

Indications

No indication recorded.