Phase 1/2RecruitingAge-related condition
Clinical Study of SNK01 in Participants With Moderate Alzheimer's Disease
A Phase I/IIa, Study to Evaluate the Safety, Tolerability and Exploratory Efficacy of SNK01 in Participants With Moderate Alzheimer's Disease
- Sponsor
- NKGen Biotech, Inc. (Industry)
- Enrolment
- 36 planned
- Conditions
- Moderate Alzheimer Disease
- Interventions
- SNK01; Placebo
- Ages
- adults, older adults
- Registry
- NCT06189963
Full record on ClinicalTrials.gov
From the registry
The goal of this clinical trial is to test SNK01 in participants with moderate Alzheimer's Disease. The main questions it aims to answer are: 1. Is SNK01 safe and tolerable when administered every 3 weeks for up to 1 year as an intravenous infusion 2. Can SNK01 administration improve cognitive assessment scores and biomarkers
Primary outcomes
- Number of participants with dose-limiting toxicity
- Maximum tolerated dose determination
- Number of participants with treatment-related adverse events as assessed by CTCAE v5.0
- Preliminary efficacy in cognitive assessment scores of CDR-SB
History
Study completion expected
Primary completion expected
Last registry update
Registered
Started