TrialSignal
Clinical trial intelligence report
A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of AL001 in C9orf72-Associated Amyotrophic Lateral Sclerosis
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 16, 2026
NCT ID
NCT05053035
Status
TERMINATED
Phase
Phase 2
Sponsor
Alector Inc.
Executive brief
Investment-Ready Snapshot
AL001, developed by Alector Inc., targets C9orf72-associated ALS, a genetic form of the disease with significant unmet medical need. The ALS market is projected to grow due to increasing prevalence and awareness, with current therapies offering limited efficacy. Alector's focus on a specific genetic mutation positions it uniquely against competitors, particularly in a landscape dominated by symptomatic treatments. The termination of this trial suggests a strategic pivot, potentially indicating challenges in meeting inclusion criteria or efficacy expectations, which may affect investor confidence and future funding.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT05053035
Indication
Amyotrophic Lateral Sclerosis
Modality
small molecule
Target
C9orf72 mutation in Amyotrophic Lateral Sclerosis (ALS)
Intervention
AL001, Placebo
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.