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Monoclonal Antibodies

Donanemab for Alzheimer's Disease

Verified Trial
Phase 3
Recruiting
Research Sponsored by Eli Lilly and Company
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
You do *not* have Alzheimer's or dementia
Answer yes if you are *not* currently enrolled in another clinical trial
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, up to week 182
Awards & highlights

Study Summary

This trial will test a new drug, donanemab, for safety and effectiveness in people with early Alzheimer's disease.

Who is the study for?
This trial is for people aged 65-80 who are at risk of Alzheimer's but don't yet have it. Participants must be able to get an MRI and do cognitive tests, not be in another study, and have a family history of Alzheimer's or early signs of amyloid and tau pathology.Check my eligibility
What is being tested?
The trial is testing Donanemab against a placebo to see if it can prevent the onset of Alzheimer's Disease in individuals who show early signs but do not yet have symptoms. The safety and effectiveness will be evaluated.See study design
What are the potential side effects?
While specific side effects for Donanemab aren't listed here, similar drugs may cause reactions at the injection site, flu-like symptoms, headache, dizziness, nausea or allergic responses.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I do not have Alzheimer's or dementia.
Select...
You can only participate in this study if you are not already taking part in another research study.
Select...
I am between 65 and 80 years old.
Select...
I am willing and able to have an MRI scan.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, up to week 182
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline, up to week 182 for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Nootropic Agents
Secondary outcome measures
Change from Baseline in Behavioral Pattern Separation-Object test (BPS-O)
Change from Baseline in CDR-Sum of Boxes (CDR-SB)
Change from Baseline in Category Fluency
+9 more

Side effects data

From 2023 Phase 3 trial • 148 Patients • NCT05108922
21%
Amyloid related imaging abnormality-oedema/effusion
14%
Covid-19
14%
Amyloid related imaging abnormality-microhaemorrhages and haemosiderin deposits
8%
Headache
7%
Infusion related reaction
4%
Arthralgia
4%
Dizziness
3%
Pneumonia
3%
Vertigo
3%
Constipation
3%
Anxiety
3%
Upper respiratory tract infection
3%
Dyspnoea
3%
Nasopharyngitis
1%
Infusion site reaction
1%
Tooth infection
1%
Chest pain
1%
Campylobacter infection
1%
Macular hole
1%
Affective disorder
1%
Hypersensitivity
1%
Pericardial effusion
1%
Urinary tract infection
1%
Feeling abnormal
1%
Food poisoning
1%
Gastritis
1%
Aspartate aminotransferase increased
1%
Deep vein thrombosis
1%
Basal cell carcinoma
1%
Mental status changes
1%
Pulmonary embolism
1%
Rib fracture
1%
Gastrooesophageal reflux disease
1%
Insomnia
1%
Sinusitis
1%
Tooth abscess
1%
Dry skin
1%
Diarrhoea
1%
Oedema peripheral
1%
Nausea
1%
Diverticulitis
1%
Pruritus
1%
Knee arthroplasty
1%
Large intestinal polypectomy
1%
Alanine aminotransferase increased
1%
Hypotension
1%
Fall
1%
Abdominal discomfort
1%
Disturbance in attention
1%
Hypertonic bladder
1%
Onychomycosis
1%
Hypertriglyceridaemia
1%
Ear infection
1%
Ingrowing nail
1%
Nephrolithiasis
1%
Syncope
1%
Palpitations
1%
Cough
1%
Skin laceration
1%
Back pain
1%
Pneumothorax
1%
Pneumomediastinum
1%
Pain in extremity
1%
Sepsis
1%
Tachycardia
1%
Meniere's disease
1%
Gout
100%
80%
60%
40%
20%
0%
Study treatment Arm
Donanemab
Aducanumab

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: DonanemabExperimental Treatment1 Intervention
Donanemab administered intravenously (IV)
Group II: PlaceboPlacebo Group1 Intervention
Placebo is administered intravenously
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Donanemab
2017
Completed Phase 3
~500

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for Alzheimer's Disease (AD) often target amyloid-beta (Aβ) plaques, which are believed to play a critical role in the disease's progression. Donanemab, for example, is an antibody that specifically targets and helps clear Aβ plaques from the brain. This mechanism is crucial because the accumulation of these plaques is associated with neuronal damage and cognitive decline in AD patients. By reducing plaque buildup, treatments like Donanemab aim to slow disease progression and preserve cognitive function. Other treatments may focus on neurotransmitter regulation, such as cholinesterase inhibitors, which increase acetylcholine levels to improve communication between nerve cells. Understanding these mechanisms helps in developing targeted therapies that can more effectively manage or potentially alter the course of Alzheimer's Disease.
Lessons Learnt from the Second Generation of Anti-Amyloid Monoclonal Antibodies Clinical Trials.

Find a Location

Who is running the clinical trial?

Eli Lilly and CompanyLead Sponsor
2,624 Previous Clinical Trials
3,214,321 Total Patients Enrolled
Study DirectorEli Lilly and Company
1,349 Previous Clinical Trials
413,080 Total Patients Enrolled

Media Library

Donanemab (Monoclonal Antibodies) Clinical Trial Eligibility Overview. Trial Name: NCT05026866 — Phase 3
Alzheimer's Disease Research Study Groups: Donanemab, Placebo
Alzheimer's Disease Clinical Trial 2023: Donanemab Highlights & Side Effects. Trial Name: NCT05026866 — Phase 3
Donanemab (Monoclonal Antibodies) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05026866 — Phase 3
Alzheimer's Disease Patient Testimony for trial: Trial Name: NCT05026866 — Phase 3
~1425 spots leftby Oct 2027