GV1001 Subcutaneous for the Treatment of Moderate to Severe Alzheimer's Disease(AD)

Samsung Pharmaceutical Co., Ltd.

Source: ClinicalTrials.gov (U.S. National Library of Medicine), data processed 2026-10-29T09:00:05; modifications: selected fields only; whitespace normalized; brief summary truncated to 2,000 characters. Not a U.S. Government endorsement.

Brief summary

The objective of this study is to evaluate the safety and efficacy of GV1001 administered subcutaneously in patients with moderate to severe Alzheimer's disease (AD).

Source: ClinicalTrials.gov (U.S. National Library of Medicine), data processed 2026-10-29T09:00:05; modifications: selected fields only; whitespace normalized; brief summary truncated to 2,000 characters. Not a U.S. Government endorsement.

Trial details

status
NOT_YET_RECRUITING
phase
PHASE3
study type
INTERVENTIONAL
enrollment
750
sponsor
Samsung Pharmaceutical Co., Ltd.
conditions
Moderate to Severe Alzheimer's Disease
interventions
DRUG: GV1001 Placebo; DRUG: GV1001 1.12mg
start date
2027-07-01
start date type
ESTIMATED
primary completion date
2028-01-01
has results
false
data source
ClinicalTrials.gov
data processed
2026-10-29T09:00:05
modifications
selected fields only; whitespace normalized; brief summary truncated to 2,000 characters

Record

Archive ID
nct:NCT05303701
Published
Mar 31, 2022
Updated
Jun 10, 2026
Venue
ClinicalTrials.gov
ClinicalTrials.gov
NCT05303701
Categories
Moderate to Severe Alzheimer's Disease
License
ClinicalTrials.gov terms (attribution, processing date, modifications noted)
Provenance
clinicaltrials

Topics