A Study to Evaluate the Safety and Efficacy of CT1812 in Subjects With Mild to Moderate Alzheimer's Disease.
Trial details
- Registry ID
- NCT03507790
- Phase
- Phase 2
Company identity has not yet been verified
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Research sample: selected versions from May 2023 onward plus a preceding baseline where available. Only selected fields were retained; endpoint measures were truncated to 300 characters. This is not complete trial or sponsor history. Daily snapshots begin when collection starts.
| Trial | Sponsor | Phase | Status | Primary completion |
|---|---|---|---|---|
| A Study to Evaluate the Safety and Efficacy of CT1812 in Subjects With Mild to Moderate Alzheimer's Disease.NCT03507790 | Cognition Therapeutics | Phase 2 | Completed | 2024-05-29Actual |
| Pilot Clinical Study of CT1812 in Mild to Moderate Alzheimer's Disease Using EEGNCT04735536 | Cognition Therapeutics | Phase 2 | Completed | 2023-04-26Actual |
| Study to Evaluate the Safety, Tolerability and Efficacy of CT1812 in Subjects With Mild to Moderate Dementia With Lewy BodiesNCT05225415 | Cognition Therapeutics | Phase 2 | Completed | 2024-11-25Actual |
| A Study to Evaluate the Safety and Efficacy of CT1812 in Early Alzheimer's DiseaseNCT05531656 | Cognition Therapeutics | Phase 2 | Active not recruiting | 2027-05-31Estimated |
| Study to Evaluate the Efficacy and Safety of Oral CT1812 in Participants With Geographic Atrophy (GA) Secondary to Dry Age-Related Macular Degeneration (AMD).NCT05893537 | Cognition Therapeutics | Phase 2 | Terminated | 2025-03-04Actual |
NCT05531656 · Cognition Therapeutics
Apr 2027
31 May 2027
NCT05225415 · Cognition Therapeutics
Text changed; whether the study measures changed has not been verified. Saved text may be shortened.
Measure: Safety and Tolerability of CT1812
Measure: Number of Study Participants With at Least One Mild, Moderate, or Severe Treatment Emergent Adverse Events (TEAEs)