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NCT07007117RECRUITINGanonymous

Phase 1 Trial of PHOX2B Peptide-Centric Chimeric Antigen Receptor Autologous T Cells (PHOX2B PC-CAR T) for Relapsed Neuroblastoma

Sponsor

Source record

Stephan Grupp MD PhD

Phase

Source record

Phase 1

Modality

AI-normalized

gene therapy

Target

AI-normalized

PHOX2B (Paired like homeobox 2B), a transcription factor specifically expressed in neuroblastoma cells.

Indication / condition

AI-normalized

Refractory Neuroblastoma

Intervention

Source record

PHOX2B PC-CAR T Cells

Source & freshness

Source record

NCT ID

NCT07007117

Original source

ClinicalTrials.gov

Source last updated

Dec 26, 2025

Ingested at

Jun 13, 2026

Internal sync

Jun 13, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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NCT ID

NCT07007117

Title

Phase 1 Trial of PHOX2B Peptide-Centric Chimeric Antigen Receptor Autologous T Cells (PHOX2B PC-CAR T) for Relapsed Neuroblastoma

Sponsor

Stephan Grupp MD PhD

Status

RECRUITING

Phase

Phase 1

Condition raw

Refractory Neuroblastoma, Relapsed Neuroblastoma, High-Risk Neuroblastoma

Condition normalized

Refractory Neuroblastoma, Relapsed Neuroblastoma, High-Risk Neuroblastoma

Modality raw

gene therapy

Modality normalized

gene therapy

Target raw

PHOX2B (Paired like homeobox 2B), a transcription factor specifically expressed in neuroblastoma cells.

Target normalized

PHOX2B (Paired like homeobox 2B), a transcription factor specifically expressed in neuroblastoma cells.

Interventions

PHOX2B PC-CAR T Cells

Public preview

Source record

The PHOX2B PC-CAR T cell therapy is positioned to address a significant unmet medical need in the treatment of relapsed high-risk neuroblastoma, a pediatric cancer with limited treatment options and poor prognosis. The trial is sponsored by a reputable institution, the Children's Hospital of Philadelphia, under the leadership of Dr. Stephan Grupp, a prominent figure in cell therapy. The potential success of this therapy could lead to a competitive advantage in the CAR T-cell market, particularly in pediatric oncology, which is currently underserved. The trial's focus on a specific patient population with defined HLA alleles may enhance the precision of treatment, potentially leading to higher response rates and improved outcomes. The market for neuroblastoma therapies is limited, but with the increasing interest in CAR T-cell therapies, successful outcomes could attract significant investment and partnerships for further development.

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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