Last updated on February 2019

Efficacy and Safety Study of Gantenerumab in Participants With Early Alzheimer's Disease (AD)


Brief description of study

This randomized, double-blind, placebo-controlled, parallel-group study will evaluate the efficacy and safety of gantenerumab versus placebo in participants with early (prodromal to mild) AD. All participants must show evidence of beta-amyloid pathology. Eligible participants will be randomized 1:1 to receive either subcutaneous (SC) injection of gantenerumab or placebo. The primary efficacy assessment will be performed at the end of the double blind period at week 104. Participants will then be offered to enter into an open-label extension (OLE). Participants not willing to go to the OLE will participate in a long term follow-up period for up to 50 weeks after the last gantenerumab dose.

Clinical Study Identifier: NCT03444870

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Reference Study ID Number: WN29922 ...

Juntendo University Urayasu Hospital
Chiba, Japan
0.56miles
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Reference Study ID Number: WN29922 ...

Tokyo Bay Advanced Medical and Makuhari Clinic
Chiba, Japan
7.07miles
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Reference Study ID Number: WN29922 ...

Tokyo Medical & Dental University Hospital
Tokyo, Japan
8.35miles
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Reference Study ID Number: WN29922 ...

Yotsuya Medical Cube
Tokyo, Japan
9.56miles
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Recruitment Status: Open


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