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NCT05053035TERMINATEDanonymous

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

Sponsor

Source record

Alector Inc.

Phase

Source record

Phase 2

Modality

AI-normalized

small molecule

Target

AI-normalized

C9orf72 mutation in Amyotrophic Lateral Sclerosis (ALS)

Indication / condition

AI-normalized

Amyotrophic Lateral Sclerosis

Intervention

Source record

AL001, Placebo

Source & freshness

Source record

NCT ID

NCT05053035

Original source

ClinicalTrials.gov

Source last updated

Jun 18, 2025

Ingested at

Jun 13, 2026

Internal sync

Jun 13, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

Open original registry record
View original source fields

NCT ID

NCT05053035

Title

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

Sponsor

Alector Inc.

Status

TERMINATED

Phase

Phase 2

Condition raw

Amyotrophic Lateral Sclerosis

Condition normalized

Amyotrophic Lateral Sclerosis

Modality raw

small molecule

Modality normalized

small molecule

Target raw

C9orf72 mutation in Amyotrophic Lateral Sclerosis (ALS)

Target normalized

C9orf72 mutation in Amyotrophic Lateral Sclerosis (ALS)

Interventions

AL001, Placebo

Public preview

Source record

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.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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