Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
A Study to Evaluate the Safety and Efficacy of CT1812 in Subjects With Mild to Moderate Alzheimer's Disease.
NCT03507790 · View on ClinicalTrials.gov ↗
Study Summary
This is a multi-center, randomized, double-blind, placebo-controlled, parallel group 36 week multicenter Phase 2 study of two doses of CT1812 in adults with mild to moderate Alzheimer's Disease (AD).
Conditions Studied
Interventions
- DRUG Placebo
- DRUG CT1812
Study Locations (20)
Florida
- JEM Research Institute — Atlantis
- Charter Research — Lady Lake
- ClinCloud, LLC — Maitland
- Allied Biomedical Research Institute — Miami
- Compass Research LLC- Bioclinica Research — The Villages
- ClinCloud — Viera
Other
- Neuro Health Centrum ltd — Brno
- NeuropsychiatrieHK S.R.O — Hradec Králové
- A-Shine S.R.O — Pilsen
- Clintrial S.R.O — Prague
Victoria
- St Vincent's Hospital Sydney — Ivanhoe
- Alfred Health — Melbourne
- Melbourne Health — Parkville
Arizona
- 21st Century Neurology/ Xenoscience Inc. — Phoenix
- Imaging Endpoints — Scottsdale
Ohio
- The Ohio State University - Wexner — Columbus
- Neuro Behavirol Clinical Research C — North Canton
Connecticut
- Ki Health Partners, LLC dba New England Institute for Clinical Research — Stamford
North Carolina
- Alzheimer's Memory Center — Charlotte
Western Australia
- Australian Alzheimer's Research Foundation — Nedlands
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 153 participants |
| Start Date | 2018-10-10 |
| Est. Completion | 2024-05-29 |
| Phase | Phase 2 |
Interested in This Trial?
Always speak with your doctor before enrolling in a clinical trial.
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03507790
The ClinicalTrials.gov registry entry for NCT03507790 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 153 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Cognition Therapeutics, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Mild to Moderate Alzheimer's Disease appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT03507790 reports 20 study locations spanning 8 distinct geographic areas — top geographies include Florida, Other, Victoria. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT03507790 about?
NCT03507790 is a clinical study titled "A Study to Evaluate the Safety and Efficacy of CT1812 in Subjects With Mild to Moderate Alzheimer's Disease.". This is a multi-center, randomized, double-blind, placebo-controlled, parallel group 36 week multicenter Phase 2 study of two doses of CT1812 in adults with mild to moderate Alzheimer's Disease (AD).
What is the current status of trial NCT03507790?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 153 participants. The study started on 2018-10-10. Estimated completion is 2024-05-29.
What conditions does trial NCT03507790 study?
This clinical trial studies the following conditions: Mild to Moderate Alzheimer's Disease. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03507790?
The interventions under investigation include: Placebo (DRUG), CT1812 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03507790?
This trial is sponsored by Cognition Therapeutics, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT03507790 being conducted?
This trial has 20 study locations across Arizona, Connecticut, Florida, North Carolina, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
How Clinical Trials Work
Understand phases 1-4, trial design, randomization, and the informed consent process.
Patient Rights in Clinical Trials
Your rights as a participant: consent, withdrawal, privacy, and who to contact.
Finding the Right Clinical Trial
A practical guide to searching trials, understanding eligibility, and evaluating options.
All Guides
Browse our complete library of clinical trial educational resources.
Read our methodology — how this data is sourced, computed, and verified.