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      A 36-week multicenter, randomized, double-blind, placebo-controlled, parallel-group, phase 3 clinical trial of sodium oligomannate for mild-to-moderate Alzheimer’s dementia

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      Alzheimer's Research & Therapy
      Springer Science and Business Media LLC

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          Abstract

          Background

          New therapies are urgently needed for Alzheimer’s disease (AD). Sodium oligomannate (GV-971) is a marine-derived oligosaccharide with a novel proposed mechanism of action. The first phase 3 clinical trial of GV-971 has been completed in China.

          Methods

          We conducted a phase 3, double-blind, placebo-controlled trial in participants with mild-to-moderate AD to assess GV-971 efficacy and safety. Participants were randomized to placebo or GV-971 (900 mg) for 36 weeks. The primary outcome was the drug-placebo difference in change from baseline on the 12-item cognitive subscale of the Alzheimer’s Disease Assessment Scale (ADAS-cog12). Secondary endpoints were drug-placebo differences on the Clinician’s Interview-Based Impression of Change with caregiver input (CIBIC+), Alzheimer’s Disease Cooperative Study-Activities of Daily Living (ADCS-ADL) scale, and Neuropsychiatric Inventory (NPI). Safety and tolerability were monitored.

          Results

          A total of 818 participants were randomized: 408 to GV-971 and 410 to placebo. A significant drug-placebo difference on the ADAS-Cog12 favoring GV-971 was present at each measurement time point, measurable at the week 4 visit and continuing throughout the trial. The difference between the groups in change from baseline was − 2.15 points (95% confidence interval, − 3.07 to − 1.23; p < 0.0001; effect size 0.531) after 36 weeks of treatment. Treatment-emergent adverse event incidence was comparable between active treatment and placebo (73.9%, 75.4%). Two deaths determined to be unrelated to drug effects occurred in the GV-971 group.

          Conclusions

          GV-971 demonstrated significant efficacy in improving cognition with sustained improvement across all observation periods of a 36-week trial. GV-971 was safe and well-tolerated.

          Trial registration

          ClinicalTrials.gov, NCT02293915. Registered on November 19, 2014

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          Most cited references45

          • Record: found
          • Abstract: not found
          • Article: not found

          A RATING SCALE FOR DEPRESSION

            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Clinical diagnosis of Alzheimer's disease: Report of the NINCDS-ADRDA Work Group* under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease

            Neurology, 34(7), 939-939
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              The Neuropsychiatric Inventory: Comprehensive assessment of psychopathology in dementia

              Neurology, 44(12), 2308-2308
                Bookmark

                Author and article information

                Contributors
                Journal
                Alzheimer's Research & Therapy
                Alz Res Therapy
                Springer Science and Business Media LLC
                1758-9193
                December 2021
                March 17 2021
                December 2021
                : 13
                : 1
                Article
                10.1186/s13195-021-00795-7
                ae1b508e-0969-42ff-96a0-945b67848f91
                © 2021

                http://creativecommons.org/licenses/by/4.0/

                http://creativecommons.org/licenses/by/4.0/

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