drugset / Trial / NCT07828470

A Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of KL0011034 Injection Administered by Continuous Infusion in Healthy Adult Subjects

NCT07828470 ↗

Phase 1 Not yet recruiting 30 enrolled Hunan Kelun Pharmaceutical Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study is a randomized, double-blind, propofol position-controlled trial, evaluating the safety, tolerability, and pharmacodynamic of continuous infusion of KL0011034 injection compared with propofol injectable emulsion for durations of 1 hour, 2 hours, and 3 hours, and evaluating the pharmacokinetic of the KL0011034 injection.

Timeline

Start
2026-10-13
Primary completion
2026-11-13
Completion
2026-11-13

Drugs

EvaluationDrugModalityDoseRoute
Subject KL0011034 Unknown — Intravenous
Subject Propofol Small molecule 2 mg/kg Intravenous

Indications

No indication recorded.