Biopharma Transcript

Alector, Inc. ALEC

Nasdaq · Pre-clinical · CNS/neurology/psychiatry · antibody · EDGAR · Updated Oct 24, 2026

Alector, Inc. (Nasdaq: ALEC) is a CNS/neurology/psychiatry drug developer. Its lead program, AL137, is in Pre-clinical for Alzheimer's disease. Its next catalyst on record is GSK collaboration: Termination effective (January 2, 2027).

Upcoming catalysts

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

Next further out: GSK collaboration — Termination effective (January 2, 2027). 3 catalysts on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
AL137 (anti-PyroGlu3 Abeta antibody + ABC)Alzheimer's diseaseantibodyPre-clinical
AL064/AL164 (tau siRNA)Alzheimer's disease and other tauopathiesRNA (siRNA/ASO/mRNA)Pre-clinical
AL050 (GCase ERT + ABC)Parkinson's disease / Lewy body dementia (GBA1)protein/peptidePre-clinical
ADP062-ABC (alpha-synuclein siRNA)Parkinson's diseaseRNA (siRNA/ASO/mRNA)Pre-clinical
ADP065-ABC (NLRP3 siRNA)Multiple neurodegenerative conditionsRNA (siRNA/ASO/mRNA)Pre-clinical

Recent results and decisions

  1. Oct 15, 2026
    n/a Alector entered into an underwriting agreement to sell 36,600,000 shares of common stock at $2.05 per share for gross proceeds of approximately $75 million.The gross proceeds from the Offering are expected to be $75,030,000.00 before deducting underwriting discounts and commissions and other offering expenses payable by the Company. Filing
  2. 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

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