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NCT05614544 · ClinicalTrials.gov registry record · Phase 1

Dose-Finding and Human Abuse Potential Study Of HSK3486 Injection In Nondependent, Recreational Central Nervous System Depressant Users

A Phase 1 study of General Anesthesia, sponsored by Haisco-USA Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
42
Enrollment target
1
Study location

NCT05614544: Completed Phase 1 study of General Anesthesia, sponsored by Haisco-USA Pharmaceuticals.

NCT05614544 is a Phase 1 study of General Anesthesia that has completed, run by Haisco-USA Pharmaceuticals. The registered enrollment target is 42 participants, below the 1,628-participant average among 4 other General Anesthesia trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05614544, a Phase 1 study of General Anesthesia, has completed, sponsored by Haisco-USA Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
42 participants
Enrollment target
1
Study location

Study Summary

Part 1: To determine the doses of IV HSK3486 and propofol for use in Part 2, the abuse potential part of the study. Part 2: To evaluate the abuse potential of HSK3486 compared with propofol when administered IV to healthy nondependent, recreational CNS depressant drug users.

Primary Outcome

To determine the doses of IV HSK3486 and propofol for use in Part 2, the abuse potential part of the study

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG Propofol
  • DRUG HSK3486

Study Locations (1)

Utah

  • ICON (LPRA) - Salt Lake - Salt Lake City

Trial Details

FieldValue
Enrollment Target 42 participants
Start Date 2022-08-16
Est. Completion 2023-10-03
Phase Phase 1
Haisco-USA Pharmaceuticals

5 total trials

What the finished NCT05614544 record still lists

NCT05614544 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 42 participants, a relatively small participant target, below the 1,628-participant average among 4 other General Anesthesia trials with a reported enrollment target (97% lower).

The record links to 1 condition, with General Anesthesia appearing as the primary indexed condition, and to 3 interventions - of which Placebo is the first listed.

NCT05614544 reports a single indexed study location in Utah.

Frequently Asked Questions

What is clinical trial NCT05614544 about?

NCT05614544 is a clinical study titled "Dose-Finding and Human Abuse Potential Study Of HSK3486 Injection In Nondependent, Recreational Central Nervous System Depressant Users". Part 1: To determine the doses of IV HSK3486 and propofol for use in Part 2, the abuse potential part of the study. Part 2: To evaluate the abuse potential of HSK3486 compared with propofol when administered IV to healthy nondependent, recreational CNS depressant drug users.

What is the current status of trial NCT05614544?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 42 participants. The study started on 2022-08-16. Estimated completion is 2023-10-03.

What conditions does trial NCT05614544 study?

This clinical trial studies the following conditions: General Anesthesia.

What interventions are being tested in trial NCT05614544?

The interventions under investigation include: Placebo (DRUG), Propofol (DRUG), HSK3486 (DRUG).

Who is sponsoring clinical trial NCT05614544?

This trial is sponsored by Haisco-USA Pharmaceuticals, which has 5 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05614544 being conducted?

This trial has 1 study location across Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for General Anesthesia

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Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

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Source: ClinicalTrials.gov NCT05614544, the US trial registry maintained by the National Library of Medicine. NCT05614544 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.