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Completed Phase 2 Interventional Results available

A Study of CST-2032 and CST-107 in Subjects With Mild Cognitive Impairment or Mild Dementia Due to Parkinson's or Alzheimer's Disease

ClinicalTrials.gov ID: NCT05104463

Public ClinicalTrials.gov record NCT05104463. 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 Jul 24, 2026, 8:12 AM 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 Phase 2a, Randomized, Placebo-Controlled, Double-Blind, Crossover Study to Evaluate the Safety, Tolerability and Effects of CST-2032 and CST-107 on Cognition in Subjects With Mild Cognitive Impairment or Mild Dementia Due to Parkinson's or Alzheimer's Disease

Study identification

NCT ID
NCT05104463
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
CuraSen Therapeutics, Inc.
Industry
Enrollment
64 participants

Conditions and interventions

Interventions

  • CST-2032, matching placebo for CST-2032, CST-107, matching placebo for CST-107 Drug

Drug

Eligibility (public fields only)

Age range
50 Years to 85 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
Apr 10, 2022
Primary completion
Dec 19, 2023
Completion
Jan 31, 2024
Last update posted
Jan 22, 2025

2022 – 2024

United States locations

U.S. sites
14
U.S. states
7
U.S. cities
14
Facility City State ZIP Site status
CuraSen Investigational Site Scottsdale Arizona 85258
CuraSen Investigational Site Lafayette California 94549
CuraSen Investigational Site Boca Raton Florida 33486
CuraSen Investigational Site Bradenton Florida 34205
CuraSen Investigational Site Lady Lake Florida 32159
CuraSen Investigational Site Miami Florida 33176
CuraSen Investigational Site New Port Richey Florida 34652
CuraSen Investigational Site Winter Park Florida 32792
CuraSen Investigational Site New York New York 10003
CuraSen Investigational Site Cincinnati Ohio 45242
CuraSen Investigational Site Houston Texas 77074
CuraSen Investigational Site Round Rock Texas 78681
CuraSen Investigational Site Stafford Texas 77477
CuraSen Investigational Site Salt Lake City Utah 84102

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05104463, 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 Jan 22, 2025 · Synced Jul 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05104463 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →