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
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.
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