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Clinical Trial 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.


Clinical Trial Description

The total duration of study period per patient is up to 28 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02667496
Study type Interventional
Source Sanofi
Contact
Status Withdrawn
Phase Phase 2
Start date November 2016
Completion date March 31, 2017

See also
  Status Clinical Trial Phase
Completed NCT01266525 - Effect of Different Doses of SAR110894 on Cognition in Patients With Mild to Moderate Alzheimer's Disease on Donepezil Phase 2