Dement Neurocogn Disord.  2023 Jul;22(3):100-108. 10.12779/dnd.2023.22.3.100.

Effects of GV1001 on Language Dysfunction in Patients With Moderate-to-Severe Alzheimer’s Disease: Post Hoc Analysis of Severe Impairment Battery Subscales

Affiliations
  • 1Department of Neurology, Hanyang University Guri Hospital, Hanyang University College of Medicine, Guri, Korea
  • 2Department of Translational Medicine, Hanyang University Graduate School of Biomedical Science & Engineering, Seoul, Korea
  • 3Department of Neurology, Inha University School of Medicine, Incheon, Korea
  • 4Department of Neurology, Ewha Womans University College of Medicine, Seoul, Korea
  • 5Department of Neurology, Bobath Memorial Hospital, Seongnam, Korea
  • 6Department of Neurology, Korea University Anam Hospital, Seoul, Korea
  • 7Department of Neurology, Soonchunhyang University Cheonan Hospital, Cheonan, Korea
  • 8Department of Neurology, Chungnam National University Hospital, Daejeon, Korea
  • 9Department of Neurology, Asan Medical Center, Seoul, Korea
  • 10Department of Neurology, Dong-A University Hospital, Busan, Korea
  • 11Department of Neurology, Myongji Hospital, Hanyang University College of Medicine, Goyang, Korea
  • 12Department of Neurology, Chonnam National University Medical School and Hospital, Gwangju, Korea
  • 13Department of Neurology, Haeundae Paik Hospital, Inje University, Buasn, Korea
  • 14Department of Neurology, Seoul Metropolitan Government-Seoul National University Boramae Medical Center, Seoul, Korea
  • 15Teloid Inc., Los Angeles, CA, USA

Abstract

Background and Purpose
The efficacy and safety of GV1001 have been demonstrated in patients with moderate-to-severe Alzheimer’s disease (AD). In this study, we aimed to further demonstrate the effectiveness of GV1001 using subscales of the Severe Impairment Battery (SIB), which is a validated measure to assess cognitive function in patients with moderate-tosevere AD.
Methods
We performed a post hoc analysis of data from a 6 month, multicenter, phase 2, randomized, double-blind, placebo-controlled trial with GV1001 (ClinicalTrials.gov, NCT03184467). Patients were randomized to receive either GV1001 or a placebo for 24 weeks. In the current study, nine subscales of SIB—social interaction, memory, orientation, language, attention, praxis, visuospatial ability, construction, and orientation to name— were compared between the treatment (GV1001 1.12 mg) and placebo groups at weeks 12 and 24. The safety endpoints for these patients were also determined based on adverse events.
Results
In addition to the considerable beneficial effect of GV1001 on the SIB total score, GV1001 1.12 mg showed the most significant effect on language function at 24 weeks compared to placebo in both the full analysis set (FAS) and per-protocol set (PPS) (p=0.017 and p=0.011, respectively). The rate of adverse events did not differ significantly between the 2 groups.
Conclusions
Patients with moderate-to-severe AD receiving GV1001 had greater language benefits than those receiving placebo, as measured using the SIB language subscale.

Keyword

GV1001; Efficacy; Alzheimer’s Disease; Language
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