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Clinical Trial Summary

This study will evaluate the safety, tolerability, and potential cognitive benefit of the experimental treatment GRF6019 in subjects with severe Alzheimer's disease.


Clinical Trial Description

This is a randomized, double-blind, placebo-controlled study to assess the safety, tolerability and potential cognitive benefit of GRF6019, a human plasma protein fraction. GRF6019 or placebo will be administered intravenously to subjects with severe Alzheimer's disease every day for 5 consecutive days. The total study duration for each subject is approximately 9 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03765762
Study type Interventional
Source Alkahest, Inc.
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Status Completed
Phase Phase 2
Start date January 15, 2019
Completion date December 17, 2019