TrialSignal
Clinical trial intelligence report
Allopregnanolone Regenerative Therapeutic for MCI/AD: Dose Finding Phase 1
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT02221622-Jul 28, 2026
NCT ID
NCT02221622
Status
COMPLETED
Phase
Phase 1
Sponsor
University of Southern California
Executive brief
Investment-Ready Snapshot
The Phase 1 trial of allopregnanolone for mild cognitive impairment (MCI) and early Alzheimer's disease (AD) aims to establish safety and tolerability, with a focus on determining the maximally tolerated dose. Given the increasing prevalence of Alzheimer's disease and the limited treatment options available, successful outcomes could position allopregnanolone as a novel therapeutic approach in a competitive market. The collaboration with the National Institute on Aging (NIA) enhances credibility and may facilitate future funding opportunities. The trial's completion in February 2018 indicates that further analysis and potential progression to later phases could attract interest from larger pharmaceutical companies looking to expand their neurology portfolios.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT02221622
Indication
Mild Cognitive Impairment
Modality
small molecule
Target
GABA-A receptor complex modulation via allopregnanolone, a naturally occurring neurosteroid.
Intervention
Allopregnanolone injection (intravenous solution), Placebo injection (intravenous solution)
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.