ID: cvn424
Aliases: CVN-424
Type: compound
Route/form: oral investigational drug
Status: investigational
Evidence level: human RCT
Best data tier: human controlled/review; exact-use indirect
Support scope: human, non-human/mechanistic
Source types: early_human, human_rct, preclinical
Linked sources: 3
Broad outcomes: Brain / mood / sleep
Reading note: These are curation notes anchored to linked sources, not a clinical recommendation or protocol.
Targets / mechanism
- GPR6 inverse agonism
- striatal indirect pathway
Optimization domains
- cognitive support
- parkinsons disease
- motor function
- early clinical
Research basis
- A phase 2 Parkinson's disease study reported acceptable tolerability and a clinically meaningful daily OFF-time signal at the 150 mg dose.
- Adds a modern CNS investigational program with human data to the graph.
Limits, risks, and missing evidence
- The study was short and small, and the endpoint is Parkinson's motor state rather than general cognition.
- Not a general nootropic despite optimization interest in CNS mechanisms.
Risk flags
- investigational
- disease specific
- limited trial duration
- CNS drug
Linked papers, labels, and reviews
- CVN424, a GPR6 inverse agonist, for Parkinson's disease and motor fluctuations
human_rct / pubmed_cvn424_phase2_2024
Double-blind randomized phase 2 trial in Parkinson's disease OFF-time. - A Phase I, First-in-Human, Healthy Volunteer Study of CVN424
early_human / pubmed_cvn424_phase1_2022
First-in-human safety, tolerability, and pharmacokinetics source for oral CVN424. - Development of CVN424: A Selective and Novel GPR6 Inverse Agonist Effective in Models of Parkinson Disease
preclinical / pubmed_cvn424_development_2021
Preclinical pharmacology and Parkinson disease model source for GPR6 inverse agonism.