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NCT04294056

A Study to Evaluate the Differences in Pharmadynamics, Pharmacokinetics, and Safety Between Ciprofol and Propofol

Completed Phase 1 Last updated 20 November 2020
What this trial tests

Phase 1 trial testing Ciprofol in Anesthesia in 18 participants. Completed in 18 September 2020.

Timeline
26 May 2020
Primary endpoint
22 June 2020
18 September 2020

Quick facts

Lead sponsorHaisco Pharmaceutical Group Co., Ltd.
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingnone
Primary purposetreatment
Enrollment18
Start date26 May 2020
Primary completion22 June 2020
Estimated completion18 September 2020
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Haisco Pharmaceutical Group Co., Ltd. — full company profile →

Who can join

Adults 18 to 45, male only, with Anesthesia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a single-center, open-label, randomized, two-stage, two-way crossover Phase I study in healthy male subjects.The main objective is to evaluate the differences in pharmadynamics (PD), pharmacokinetics (PK), and safety between ciprofol injectable emulsion and propofol injectable emulsion at different doses in healthy subjects.

Publications & conference data

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

  1. Effects of Cipepofol on Cardiac Depolarization and Repolarization in Healthy Subjects: A Single-Center, Randomized, Placebo and Positive-Controlled Thorough QT Study.
    Kleiman R, Rudo T, Daley W, Hu M, et al · · 2026 · PMID 41858914 · DOI 10.2147/dddt.s565051

Verify or expand the search:

Other trials of Ciprofol

Trials testing the same drug.

Other recruiting trials for Anesthesia

Currently open trials in the same condition.

Other Haisco Pharmaceutical Group Co., Ltd. trials

Trials by the same sponsor.

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Data sources for this page

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