Recent Updates
Recently added Catalysts

CHI-554

Phase 2

Anxiety | Small molecule | Psychiatry |Canopy Growth Corporation Common Shares|Last Updated: Jun 2, 2021

Success Probability

Subscribe to view

Market & Valuation

Subscribe to view

Trial Design

UNCONTROLLED
Total Trials1
Total Enrollment84

FDA Designations

No designations recorded

Clinical trial landscape

CHI-554 · 1 trial · 3 indications

Phase 2 1
NCT04577612A Randomized Controlled Test of the Effects of CHI-554 on Fear.Anxiety
COMPLETED84 Analytics
PHASE2COMPLETED
A Randomized Controlled Test of the Effects of CHI-554 on Fear.
AnxietyUnlock trial analytics

Study Design & Arms

Interventions

NameTypeDescription
CHI-554DRUGhemp-derived CBD in MCT oil
Unlock Study Design Details

Frequently asked questions about CHI-554

What is CHI-554 used for?

CHI-554 is an investigational small molecule being developed for the treatment of anxiety. It is in Phase 2 clinical development, and a completed trial has studied its effects on fear, anxiety, and panic. The drug is not approved and remains under investigation.

Who makes CHI-554?

CHI-554 is being developed by Canopy Growth Corporation, traded under the ticker CGC. The company is conducting clinical research on this investigational drug for anxiety, with a Phase 2 trial already completed.

What phase is CHI-554 in?

CHI-554 is in Phase 2 clinical development. One Phase 2 trial has been completed, and the drug is still investigational, meaning it has not been approved for any use. The completed trial enrolled 84 participants.

What clinical trials is CHI-554 in?

CHI-554 has one completed Phase 2 trial, identified as NCT04577612, titled "A Randomized Controlled Test of the Effects of CHI-554 on Fear." The trial studied conditions including anxiety, fear, and panic, with an enrollment of 84 participants.

Is CHI-554 FDA approved?

No, CHI-554 is not FDA approved. It is an investigational drug in Phase 2 clinical development for anxiety. A Phase 2 trial has been completed, but the drug has not received regulatory approval and remains under study.