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Terminated Phase 1Phase 2 Interventional

A Phase 1b Study of the NLRP3 Inhibitor VENT-02 in Patients With Mild to Moderate Parkinson's Disease

ClinicalTrials.gov ID: NCT06822517

Public ClinicalTrials.gov record NCT06822517. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 9, 2026, 2:55 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind, Placebo-Controlled, Phase 1b Study of the NLRP3 Inhibitor VENT-02 in Patients With Mild to Moderate Parkinson's Disease

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This trial is a randomized, double-blind, placebo-controlled Phase 1b study evaluating the safety/tolerability, PK, and pharmacodynamics of VENT 02, administered orally at 1 dose level twice daily (BID) over 28 days in patients with mild to moderate Parkinson's disease. The study includes a screening period, a 28-day double-blind treatment period, and a 7-day follow-up period after last dose. Approximately 30 patients will be randomized into 1 of the 2 treatment arms.

Study identification

NCT ID
NCT06822517
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Ventus Therapeutics U.S., Inc.
Industry
Enrollment
29 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
45 Years to 90 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 5, 2025 (Actual)
Primary completion
Oct 9, 2025 (Actual)
Completion
Oct 9, 2025 (Actual)
Last update posted
Oct 29, 2025

2025

United States locations

U.S. sites
23
U.S. states
9
U.S. cities
22
Facility City State ZIP Site status
Investigative Site Fountain Valley California 92708 —
Investigative Site San Jose California 95124 —
Investigative Site West Hills California 91307 —
Investigative Site Englewood Colorado 80113 —
Investigative Site Aventura Florida 33180 —
Investigative Site Boca Raton Florida 33486 —
Investigative Site Coral Gables Florida 33134 —
Investigative Site Coral Springs Florida 33067 —
Investigative Site Cutler Bay Florida 33189 —
Investigative Site Daytona Beach Florida 32117 —
Investigative Site Doral Florida 33178 —
Investigative Site Jacksonville Florida 32256 —
Investigative Site Maitland Florida 32751 —
Investigative Site Miami Florida 33135 —
Investigative Site Miami Florida 33165 —
Investigative Site Winter Park Florida 32789 —
Investigative Site Scarborough Maine 04074 —
Investigative Site Farmington Hills Michigan 48334 —
Investigative Site Abington Pennsylvania 19001 —
Investigative Site Memphis Tennessee 38157 —
Investigative Site Cypress Texas 77429 —
Investigative Site Round Rock Texas 78681 —
Investigative Site Spokane Washington 99202 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06822517, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 29, 2025 · Synced Oct 9, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06822517 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →