drugset / Trial / NCT02667496

Safety Study of Sargramostim in Treating Patients With Mild Cognitive Impairment Due to Alzheimer's Disease

NCT02667496 ↗

RandomizedParallel-groupQuadruple-blindTreatment

Summary

Primary Objective: To compare the effect of repeat doses of Leukine to placebo administered subcutaneously (SC) on established cortical amyloid load in patients with mild cognitive impairment (MCI) due to Alzheimer's disease (AD). Secondary Objective: * To evaluate safety and tolerability of Leukine versus placebo. * To explore the effect of Leukine versus placebo on cognitive performance. * To collect biospecimens for future biomarker research.

Timeline

Start
2016-11
Primary completion
2017-03-31
Completion
2017-03-31

Outcome

Outcome not reported

Stopped (Enrollment): “Slow recruitment”

Drugs

EvaluationDrugModalityDoseRoute
Subject sargramostim Protein / enzyme biologic — Subcutaneous

Indications