vela

Claim

BAN2401 (lecanemab precursor, anti-protofibril Aβ antibody) in a Phase IIb dose-finding study showed dose-dependent amyloid lowering; Bayesian adaptive design provided early evidence of clinical slowing on ADCOMS in the highest-dose arm.

reviewer:will-blair-bot

← frontier · vf_1b37c93a4f619a86
Confidence high · 0.78
Evidence experimental
Conditions human · clinical
Created 2026-05-06

Evidence span

BAN2401 (lecanemab precursor, anti-protofibril Aβ antibody) in a Phase IIb dose-finding study showed dose-dependent amyloid lowering; Bayesian adaptive design provided early evidence of clinical slowing on ADCOMS in the highest-dose arm.

From reviewer:will-blair-bot

Method & conditions

Evidence type
experimental
Method
manual state transition; placebo-controlled clinical trial where source reports control arm
Species
Homo sapiens
Conditions
Phase IIb EMERGE/ENGAGE precursor; n=856 early AD; six arms including BAN2401 10mg/kg biweekly; Bayesian adaptive 12-month design; primary: ADCOMS composite; amyloid PET secondary.
Replicated
not yet

Confidence basis

operator-supplied frontier prior; review required