Head-to-head evidence
ACI-35.030 vs Etalanetug
Same mechanism, same race: design-graded trial evidence for both assets, with the grading rationale shown. Grades describe the quality of the evidence, never the merits of either security.
Alzheimer's Disease
Shared mechanism: Tau (monoclonal antibody) · full Alzheimer's Disease pipeline
ACI-35.030
Developed by AC Immune and partners
NCT04445831 · Phase 1/2 · completed
This was a randomized, quadruple-blinded, placebo-controlled study, which is a strong design foundation, but the enrollment was very small (57 participants split across seven arms, several with only 4-6 subjects), and the primary endpoints were safety/tolerability counts and antibody-titer levels rather than a hard clinical or cognitive outcome - cognitive and functional scales (CDR-SB, RBANS, NPI) were only exploratory and their results were not even posted. Because the primary comparisons here are immunogenicity/safety readouts rather than a statistically tested clinical efficacy endpoint, this evidence is real but limited.
Etalanetug
Developed by Eisai
NCT04971733 · Phase 1/2 · completed
The study treated 8 participants with E2814 in open-label, single-arm cohorts without randomization, blinding, or a comparator, and its biomarker primary endpoint was not a controlled clinical comparison. Because the named drug is Etalanetug but the trial intervention was E2814, these results are not direct evidence for Etalanetug.
Next expected readout: December 2026 · NCT06602258 (registry estimate)
The full competitive landscape for each asset (every same-race competitor with aligned evidence, sortable) is on the asset pages: ACI-35.030's landscape · Etalanetug's landscape