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RecruitingNCT05908695

An Efficacy and Safety Study of Sodium Oligomannate (GV-971) for the Treatment of Alzheimer's Disease

A 36-week, Multi-center, Randomized, Double-blind, Placebo-controlled, Parallel-group Clinical Trial to Evaluate the Efficacy and Safety of Sodium Oligomannate (GV-971) in Treatment of Mild to Moderate Alzheimer's Disease

Status
Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
1,312 (estimated)
Sponsor
Green Valley (Shanghai) Pharmaceuticals Co., Ltd. · Industry
Sex
All
Age
50 Years – 85 Years
Healthy volunteers
Not accepted

Summary

The primary purpose of this study is to confirm the clinical efficacy and mechanism of action of GV-971, and identify incidence of known adverse reactions in long-term use and observe new adverse reactions, providing more guidance for clinical use.

Conditions

Interventions

TypeNameDescription
DRUGGV-971Administered PO
DRUGPlaceboAdministered PO

Timeline

Start date
2023-08-31
Primary completion
2029-06-01
Completion
2029-12-01
First posted
2023-06-18
Last updated
2023-11-09

Locations

50 sites across 1 country: China

Source: ClinicalTrials.gov record NCT05908695. Inclusion in this directory is not an endorsement.

An Efficacy and Safety Study of Sodium Oligomannate (GV-971) for the Treatment of Alzheimer's Disease (NCT05908695) · Clinical Trials Directory