Study identifier:16557
ClinicalTrials.gov identifier:NCT02972658
EudraCT identifier:2016-003440-36
CTIS identifier:N/A
A Randomized, Double-Blind, Delayed-Start Study of LY3314814 (AZD3293) in Early Alzheimer’s Disease Dementia (Extension of Study AZES, The AMARANTH Study)
Alzheimer's disease
Phase 3
No
Lanabecestat
All
421
Interventional
55 Years +
Allocation: Randomized
Endpoint Classification: -
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment
Verified 01 Nov 2019 by AstraZeneca
AstraZeneca
Eli Lilly and Company
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: AZES Lanabecestat 20 milligrams (mg)/AZFD Lanabecestat 20 mg Participants who received Lanabecestat 20 mg in the feeder study (AZES) were randomized to receive Lanabecestat 20 mg. | Drug: Lanabecestat Administered orally Other Name: LY3314814 Other Name: AZD3293 |
Experimental: AZES Lanabecestat 50 mg/AZFD Lanabecestat 50 mg Participants who received Lanabecestat 50 mg in the feeder study (AZES) were randomized to receive Lanabecestat 50 mg. | Drug: Lanabecestat Administered orally Other Name: LY3314814 Other Name: AZD3293 |
Experimental: AZES Placebo/AZFD Lanabecestat 20 mg Participants who received placebo in the feeder study (AZES) were randomized to receive Lanabecestat 20 mg. | Drug: Lanabecestat Administered orally Other Name: LY3314814 Other Name: AZD3293 |
Experimental: AZES Placebo/AZFD Lanabecestat 50 mg Participants who received placebo in the feeder study (AZES) were randomized to receive Lanabecestat 50 mg. | Drug: Lanabecestat Administered orally Other Name: LY3314814 Other Name: AZD3293 |