Biopharma Transcript

Alector, Inc. ALEC

Nasdaq · Phase 1 · CNS/neurology/psychiatry · antibody · EDGAR · Updated Nov 6, 2026

Alector, Inc. (Nasdaq: ALEC) is a CNS/neurology/psychiatry drug developer. Its lead program, AL137, is in Phase 1 for Alzheimer's disease. Its next catalyst on record is AL137: First-in-human subcutaneous dosing in Australia (April 2027).

Upcoming catalysts

No catalyst is dated to the next 30 days or to an FDA action date.

Next further out: AL137 — First-in-human subcutaneous dosing in Australia (April 2027). 4 catalysts on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
latozinemab (AL001)Frontotemporal dementia due to GRN mutation (FTD-GRN)antibodyPhase 3
nivisnebart (AL101/GSK4527226)Alzheimer's diseaseantibodyPhase 2
AL137Alzheimer's disease (amyloid beta targeting)antibodyPhase 1
AL164Alzheimer's disease and other tauopathies (tau siRNA)RNA (siRNA)Pre-clinical
AL062Parkinson's disease and Lewy body dementia (alpha-synuclein siRNA)RNA (siRNA)Pre-clinical
ADP065-ABCMultiple neurodegenerative conditions (NLRP3 siRNA)RNA (siRNA)Pre-clinical
AL050Parkinson's disease (GCase deficiency)protein/peptidePre-clinical
AL037Alzheimer's disease (amyloid beta targeting, backup to AL137)antibodyPre-clinical

Recent results and decisions

  1. Oct 21, 2025
    missed INFRONT-3 Phase 3 missed the clinical co-primary endpoint (CDR plus NACC FTLD-SB); plasma progranulin co-primary was significant but no effect on secondary/exploratory biomarkers or vMRI; OLE and continuation study discontinued.did not meet the clinical co-primary endpoint of slowing FTD-GRN progression Filing

For subscribers

Other phase 1 CNS/neurology/psychiatry companies