drugset / Trial / NCT05811442

Study of 50561 in Patients With Mild or Moderate Alzheimer's Disease

NCT05811442 ↗

Phase 2 Completed 68 enrolled Beijing Joekai Biotechnology LLC
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a multi-center, Phase IIa, randomized, double-blind, placebo-controlled study designed to evaluate the efficacy, safety of two doses of 50561 compared to placebo in participants diagnosed with mild to moderate Alzheimer's disease.

Timeline

Start
2023-04-18
Primary completion
2025-08-22
Completion
2025-09-11

Drugs

EvaluationDrugModalityDoseRoute
Subject 50561 Unknown 128 mg —
Subject 50561 Unknown 256 mg —

Indications