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Clinical trial intelligence report
A Phase 1, Double-Blind, Placebo-Controlled, Single-Ascending-Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of BIIB100 Administered Orally to Adult Participants With Amyotrophic Lateral Sclerosis
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT03945279-Jul 28, 2026
NCT ID
NCT03945279
Status
COMPLETED
Phase
Phase 1
Sponsor
Biogen
Executive brief
Investment-Ready Snapshot
BIIB100, developed by Biogen, is currently in Phase 1 clinical trials for the treatment of amyotrophic lateral sclerosis (ALS). The market for ALS therapies is growing, driven by increasing awareness and diagnosis rates, alongside a limited number of effective treatment options. The competitive landscape includes established therapies like riluzole and edaravone, but there remains a significant unmet need for novel treatments that can improve patient outcomes. Successful completion of this trial could position Biogen favorably in the ALS market, potentially leading to partnerships or acquisition interest from larger pharmaceutical companies. Diligence should focus on the safety and tolerability profile of BIIB100, as well as its pharmacokinetic characteristics, which will be critical for future development stages.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT03945279
Indication
Amyotrophic Lateral Sclerosis
Modality
small molecule
Target
Not specified in the provided data; further investigation required to determine the precise molecular or mechanistic target profile of BIIB100.
Intervention
BIIB100, 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.