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A clinical trial to look at the long-term effects of gantenerumab in people with Alzheimer’s disease
A Study to Evaluate the Safety and Tolerability of Long-term Administration of Gantenerumab in Participants With Alzheimer's Disease (AD)
- Neurodegenerative Disorder
- Alzheimer's Disease (AD)
Please note that the recruitment status of the trial at your site may differ from the overall study status because some study sites may recruit earlier than others.
Trial Status:
Terminated
This trial runs in
Cities
- Amsterdam
- Austin
- Baggiovara
- Barcelona
- Basel
- Brescia
- Buenos Aires
- Castellanza
- Chiba
- Chihuahua
- Elche
- Halifax
- Incheon
- İstanbul
- ivanhoe
- İzmir
- Kalamazoo
- København
- Las Condes
- Lombardia
- London
- Los Angeles
- Madrid
- matthews
- Memphis
- Monterrey
- New York
- Newcastle upon Tyne
- Orlando
- Otake
- penarth
- Peterborough
- Poznań
- Québec
- Saint Petersburg
- Samsun
- Sankt-Peterburg
- Seoul
- Sun City
- Tampa
- Terrassa
- The Villages
- Toronto
- Tulsa
- Urayasu
- València
- warrington
- Warszawa
- Woodville South
Trial Identifier:
NCT04339413 WN41874
Trial Summary
The main purpose of the study was to evaluate the safety and tolerability of long-term administration of gantenerumab in participants with AD. All participants who have completed the open-label extensions (OLEs) of studies WN25203 or WN28745 were enrolled in Part 1 of this study. Of these, participants who completed Week 104 visit in Part 1. Participants received open-label gantenerumab by subcutaneous (SC) injection every four weeks (Q4W) at the same dose as administered in the parent studies (part 1)/ Week 104 visit.
Hoffmann-La Roche
Sponsor
Phase 3
Phase
NCT04339413, WN41874
Trial Identifier
Gantenerumab
Treatments
Alzheimer Disease
Condition
Official Title
An Open-Label, Multicenter, Rollover Study to Evaluate the Safety and Tolerability of Long-Term Administration of Gantenerumab in Participants With Alzheimer's Disease
Eligibility Criteria
All
Gender
No
Healthy Volunteers
Inclusion Criteria
- Part 1: Participants who completed the open-label extensions (OLEs) of studies WN25203 or WN28745 will be eligible to participate in Part 1 of the study
- Part 2: All participants who have completed Week 104 visit in Part 1 will be eligible for Part 2 of the study
- For Part 1 and Part 2:
- For women of childbearing potential: agreement to remain abstinent (refrain from heterosexual intercourse) or use contraceptive methods that result in a failure rate of <1% per year during the treatment period and for at least 16 weeks after the last dose of study drug
- Agreement to not donate blood or blood products for transfusion for the duration of the study and for 1 year after final dose of study drug
- Availability of a person ('caregiver') who in the investigator's judgement, has frequent and sufficient contact with the participant
Exclusion Criteria
- Prematurely discontinued from the OLEs of studies WN25203 or WN28745 or from study drug for any reason
- Any medical condition that may jeopardize the participant's safety if he or she continues to receive study treatment
- If the participant is unlikely to benefit from gantenerumab therapy, based on disease progression or other factors, or if study participation is otherwise not in the participant's best interest
- Any investigational treatment other than gantenerumab during or since completion of the OLEs of studies WN25203 or WN28745
- Pregnancy
- Evidence of disseminated leptomeningeal hemosiderosis (i.e., more than three focal leptomeningeal hemosiderosis)
- Evidence of intracerebral macrohemorrhage
- Part 2: Participants who have been discontinued from Part 1 of the study
For the latest version of this information please go to www.forpatients.roche.com