drugset / Trial / NCT02221622
Allopregnanolone for Mild Cognitive Impairment Due to Alzheimer's Disease or Mild AD
Phase 1
Completed
24 enrolled
University of Southern California
National Institute on Aging (NIA) · collab
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |