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A Study of a Potential Disease Modifying Treatment in Individuals at Risk for or With a Type of Early Onset AD Caused by a Genetic Mutation

Study acronym: DIAN-TU-002
StatusRecruiting
PhasePhase 2/3
Started2024-11-22
View on ClinicalTrials.gov ↗
The purpose of this research study is to test the study drug, referred to as remternetug, to determine its effectiveness for the study treatment of asymptomatic (at risk) Alzheimer disease in individuals with AD-causing mutations. This study will also investigate the effects of remternetug on biomarkers (measures of the disease including brain scans, blood and spinal fluid tests), examine safety data to identify any potential benefits or risks, and examine how well participants can tolerate remternetug. Stage 1 will determine if treatment with the study drug prevents or reverses amyloid beta (Aβ) accumulation compared with placebo in participants with dominantly inherited Alzheimer's disease (DIAD). Stage 2 will evaluate the effect of early anti-amyloid treatment on downstream biomarkers of AD in treated participants compared to external control groups.

Amendment record

Amended 7 times since 2024-10-15; most recent filed 2026-07-23. Every amendment is listed below.

Dates here are the day the sponsor filed the amendment, not the day ClinicalTrials.gov published it. Version history last read from ClinicalTrials.gov on 2026-08-30.

2026-07-23
Amendment Study Status, Eligibility, Contacts/Locations v7
2026-02-11
Amendment Study Status, Arms and Interventions, Contacts/Locations v6
2025-11-10
Amendment Study Status, Oversight, Contacts/Locations v5
2025-07-30
Amendment Study Status, Oversight, Arms and Interventions, Contacts/Locations v4
2025-03-31
Amendment Study Status, Contacts/Locations v3
2024-11-25
Amendment Not Yet RecruitingRecruiting Study Status, Sponsor/Collaborators, Outcome Measures, Eligibility, Contacts/Locations v2
2024-10-17
Amendment Study Identification, Study Status v1
2024-10-15
Original filing
Trial Details
NCT Number NCT06647498
Lead Sponsor Washington University School of Medicine
Collaborators: Alzheimer's Association, Eli Lilly and Company, National Institute on Aging (NIA), GHR Foundation, Private Donors
Conditions Alzheimers Disease, Dementia, Alzheimers Disease, Familial
Enrollment 280 participants
Start Date 2024-11-22
Primary Completion 2034-03 (estimated)
Study Completion 2034-08 (estimated)
Updated on ClinicalTrials.gov 2026-07-27