TrialSignal
Clinical trial intelligence report
Phase I Study of Autologous T Lymphocytes Expressing GD2-specific Chimeric Antigen and Constitutively Active IL-7 Receptors for the Treatment of Patients With Relapsed or Refractory Neuroblastoma and Other GD2 Positive Solid Cancers(GAIL-N)
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT03635632-Jul 28, 2026
NCT ID
NCT03635632
Status
ACTIVE_NOT_RECRUITING
Phase
Phase 1
Sponsor
Baylor College of Medicine
Executive brief
Investment-Ready Snapshot
The GAIL-N trial, sponsored by Baylor College of Medicine, focuses on a novel gene therapy approach using autologous T lymphocytes engineered to express GD2-specific CAR and IL-7 receptors for treating relapsed or refractory neuroblastoma and other GD2-positive solid tumors. Given the lack of standard treatment options for these patient populations, the potential market for GD2-targeted therapies is significant. The competitive landscape includes existing CAR T-cell therapies and emerging immunotherapies targeting similar pathways. Successful outcomes could position this therapy as a leading option in a niche but critical segment of oncology, particularly for pediatric cancers. Diligence should focus on the trial's safety profile, efficacy data, and potential for regulatory approval, as well as the scalability of T-cell manufacturing processes.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT03635632
Indication
Relapsed Neuroblastoma
Modality
gene therapy
Target
GD2-specific Chimeric Antigen Receptor (CAR) and Constitutively Active IL-7 Receptors
Intervention
C7R-GD2.CART cells
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.