drugset / Trial / NCT01429623

A 3 Year Study to Evaluate the Safety and Efficacy of Low Dose Ladostigil in Patients With Mild Cognitive Impairment

NCT01429623 ↗

Phase 2 Completed 210 enrolled Avraham Pharmaceuticals Ltd
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine whether treatment with the investigational drug ladostigil will delay the onset of Alzheimer's disease(AD) in patients with Mild Cognitive Impairment (MCI). MCI is now recognized as a precursor to AD and clinical tools are available to assess cognitive performance at this earlier stage. Ladostigil is currently under investigation for the treatment of AD. In this study, the investigators will be examining ladostigil at a lower dose level. At this dose level, ladostigil has been shown to reduce signs of early memory loss in animals. Thus, in this study the investigators are attempting to determine if earlier invention with a lower dose of ladostigil will significantly reduce initial memory loss and delay the subsequent progression to more serious cognitive dysfunction.

Timeline

Start
2012-02
Primary completion
2016-07
Completion
2016-09

Outcome

Missed primary endpoint

paper After 36 months, 21 of 103 patients on placebo and 14 of 99 patients receiving ladostigil progressed to Alzheimer disease (log-rank test p = 0.162). PMID 31492718 ↗

paper CONCLUSION: Ladostigil was safe and well tolerated but did not delay progression to dementia. PMID 31492718 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject ladostigil Small molecule 10 mg —