drugset / Trial / NCT06427668

Study of SPG302 in Adult Participants With Mild-to-Moderate Alzheimer's Disease (AD)

NCT06427668 ↗

Phase 2 Active not recruiting 24 enrolled Spinogenix
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This phase 2 study will evaluate the safety, tolerability, clinical efficacy, pharmacokinetics, and pharmacodynamics of SPG302 in adult participants with mild-to-moderate AD.

Timeline

Start
2024-07-29
Primary completion
2025-12
Completion
2026-06

Drugs

EvaluationDrugModalityDoseRoute
Subject SPG302 Small molecule 300 mg Oral

Indications