drugset / Trial / NCT02667496
Safety Study of Sargramostim in Treating Patients With Mild Cognitive Impairment Due to Alzheimer's Disease
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | sargramostim | Protein / enzyme biologic | — | Subcutaneous |