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A Phase I Trial to Evaluate Safety and Tolerability of Abatacept Followed by Subcutaneous Interleukin-2 Administration in Patients With Amyotrophic Lateral Sclerosis
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT06307301-Jul 28, 2026
NCT ID
NCT06307301
Status
COMPLETED
Phase
Phase 1
Sponsor
The Methodist Hospital Research Institute
Executive brief
Investment-Ready Snapshot
The Phase 1 trial, sponsored by The Methodist Hospital Research Institute, investigates the safety and tolerability of a combination therapy involving abatacept (Orencia) and subcutaneous IL-2 in ALS patients. Given the urgent need for effective treatments in ALS, which currently has limited therapeutic options, this trial could position the sponsor favorably within the niche ALS market. If successful, the findings may lead to further development and potential commercialization of this combination therapy, addressing a significant unmet medical need. Competitive implications include potential partnerships or licensing opportunities, particularly with companies focused on immunotherapy and neurodegenerative diseases. Diligence should focus on regulatory pathways and reimbursement strategies for ALS therapies.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT06307301
Indication
Amyotrophic Lateral Sclerosis
Modality
small molecule
Target
Regulatory T-lymphocytes (Tregs) and immune modulation in Amyotrophic Lateral Sclerosis (ALS)
Intervention
Abatacept Injection [Orencia] and Proleukin (aldesleukin)
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.