drugset / Trial / NCT02221622

Allopregnanolone for Mild Cognitive Impairment Due to Alzheimer's Disease or Mild AD

NCT02221622 ↗

RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the safety and tolerability of allopregnanolone, a naturally occurring brain steroid, in mild cognitive impairment and early Alzheimer's disease participants. The primary goal is to determine the maximally tolerated dose.

Timeline

Start
2014-08
Primary completion
2018-02
Completion
2018-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Allopregnanolone Small molecule 2 mg Intravenous
Subject Allopregnanolone Small molecule 4 mg Intravenous
Subject Allopregnanolone Small molecule 6 mg Intravenous
Subject Allopregnanolone Small molecule 10 mg Intravenous
Subject Allopregnanolone Small molecule 14 mg Intravenous