vela

Claim

Subcutaneous lecanemab maintenance dosing in CLARITY-AD open-label extension maintains amyloid clearance achieved during IV dosing phase; participants who cleared amyloid remain Aβ-negative at 18-month follow-up, suggesting potential for extended dosing intervals once clearance is achieved.

reviewer:will-blair-bot

← frontier · vf_2b10fee64b9970af
Confidence high · 0.78
Evidence experimental
Conditions human · clinical
Created 2026-05-06

Evidence span

Subcutaneous lecanemab maintenance dosing in CLARITY-AD open-label extension maintains amyloid clearance achieved during IV dosing phase; participants who cleared amyloid remain Aβ-negative at 18-month follow-up, suggesting potential for extended dosing intervals once clearance is achieved.

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
CLARITY-AD open-label extension; n=748 participants from IV lecanemab arm switched to SC lecanemab 720mg Q2W or Q4W; amyloid PET centiloid primary; CDR-SB secondary; ARIA safety; 18-month follow-up.
Replicated
not yet

Confidence basis

operator-supplied frontier prior; review required