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donanemab

Generic: donanemab·Brand: Kisunla

donanemab: 9 clinical trials tracked.

donanemab evidence translation

What we can confirm

9 tracked trials

No verified listed company relationship

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about donanemab, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence8 indications · 0 study sponsors
Clinical Trial Registry Records (9)

Alzheimer's Tau Platform (ATP): Regimen Specific Appendix for AADvac1

NCT07167966Registry updated 2026-09-08·Phase 2
Enrolling by invitation

Primary endpoint: Reduction of brain tau deposition as measured by tau positron emission tomography (PET)

InterventionalRandomizedquadruple450 targetStarted 2026-11Completion 2028-083 sites · United StatesPaul S. Aisen

A Phase 4, Multicenter, Open-Label, Single-Arm Study to Evaluate the Safety and Tolerability of Donanemab in Indian Participants With Early Symptomatic Alzheimer's Disease

NCT07838155Registry updated 2026-09-24·Phase 4
Not yet recruiting

Primary endpoint: Number of Participants with Any Occurrence of Amyloid-Related Imaging Abnormalities (ARIA)

Interventionalopen50 targetStarted 2026-10Completion 2030-079 sites · IndiaEli Lilly and Company

An Annual Dosing Study of Donanemab in Participants Who Completed Donanemab Study AACM

NCT07602582Registry updated 2026-07-07·Phase 3
Recruiting

Primary endpoint: Change from Baseline as Measured by Clinical Dementia Rating - Sum of Boxes (CDR-SB)

InterventionalRandomizeddouble550 targetStarted 2026-05Completion 2029-0950 sites · United StatesEli Lilly and Company

A Phase 2 Randomized, Placebo-Controlled Clinical Trial to Assess the Safety and Efficacy of Donanemab in Participants With Early Cognitive Decline, at Least One Core Clinical Feature of Dementia With Lewy Bodies, and Confirmation of Alpha-Synuclein and Amyloid Co-pathology

NCT07589595Registry updated 2026-10-08·Phase 2
Recruiting

Primary endpoint: Change from Baseline on Clinical Dementia Rating - Sum of Boxes (CDR-SB)

InterventionalRandomizedquadruple350 targetStarted 2026-05Completion 2028-0872 sites · Japan, South Korea, Taiwan, United StatesEli Lilly and Company

A Study of Donanemab Versus Placebo in Chinese Participants at Risk for Cognitive and Functional Decline of Alzheimer's Disease

NCT07571161Registry updated 2026-08-24·Phase 3
Recruiting

Primary endpoint: Time to Clinical Progression as Measured by Clinical Dementia Rating-Global Score (CDR-GS)

InterventionalRandomizeddouble140 targetStarted 2026-04Completion 2030-0430 sites · ChinaEli Lilly and Company

Investigating the Effect of Different Donanemab Dosing Regimens on ARIA-E and Amyloid Lowering in Adults With Early Symptomatic Alzheimer's Disease

NCT05738486Registry updated 2026-06-18·Phase 3
Active, not recruiting

Primary endpoint: Percentage of Participants With Any Occurrence of Amyloid-Related Imaging Abnormality-Edema/Effusion (ARIA-E)

InterventionalRandomizeddouble1,175 targetStarted 2023-02Completion 2027-0549 sites · United Kingdom, United StatesEli Lilly and Company

Global Study to Investigate Safety and Efficacy of Donanemab in Early Symptomatic Alzheimer's Disease

NCT05508789Registry updated 2026-09-22·Phase 3
Active, not recruiting

Primary endpoint: Change from Baseline on the Integrated Alzheimer's Disease Rating Scale (iADRS)

InterventionalRandomizeddouble1,500 targetStarted 2022-10Completion 2028-0750 sites · Argentina, Australia, ChinaEli Lilly and Company

Assessment of Safety, Tolerability, and Efficacy of Donanemab in Early Symptomatic Alzheimer's Disease

NCT04437511Registry updated 2026-08-26·Phase 3
Active, not recruiting

Primary endpoint: Change From Baseline on the Integrated Alzheimer's Disease Rating Scale (iADRS) (Overall Population)

InterventionalRandomizeddouble1,736 enrolledStarted 2020-06Completion 2028-1150 sites · United StatesEli Lilly and Company

Assessment of Safety, Tolerability and Efficacy of LY3002813 in Early Symptomatic Alzheimer's Disease

NCT03367403Registry updated 2026-03-19·Phase 2
Completed

Primary endpoint: Change From Baseline in the Integrated Alzheimer's Disease Rating Scale (iADRS) Score

InterventionalRandomizeddouble272 enrolledStarted 2017-12Completion 2021-0950 sites · United StatesEli Lilly and Company