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NCT05642455RecruitingPhase 1/2

SPEARHEAD-3 Pediatric Study

A Phase 1/2 Open Label, Basket Study to Assess the Safety, Tolerability and Anti-Tumor Activity of Afamitresgene Autoleucel in Pediatric Subjects With MAGE-A4 Positive Tumors

Source: ClinicalTrials.gov · Last updated 11 Aug 2026

Brief summary (registry, in English)

This is a pediatric basket study to investigate the safety and efficacy of afamitresgene autoleucel in HLA-A\*02 eligible and MAGE-A4 positive subjects aged 2-17 years of age with advanced cancers.

Status (registry)
Recruiting
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
20 (estimated)
First submitted
7 Nov 2022
Start date
1 Sept 2023
Primary completion date
1 Oct 2026
Lead sponsor
USWM CT, LLC
NCT number
NCT05642455

What you commit to

  • Study type: Interventional · Phase 1/2
  • Planned participants: 20
  • From 1 Sept 2023 to the primary completion date, 1 Oct 2026
  • 10 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to fludarabine, cyclophosphamide.
  • History of autoimmune or immune mediated disease
  • Other prior malignancy that is not considered by the Investigator to be in complete remission
  • Clinically significant cardiovascular disease
  • Active infection with human immunodeficiency virus, hepatitis B virus, hepatitis C virus, or human T cell leukemia virus
  • Experiencing ongoing rapid disease progression that in the opinion of the Investigator significantly increases the subjects risk associated with treatment.

Other

  • Positive for HLA-A\*02:05 in either allele; or any A\*02 having same protein sequence as HLA-A\*02:05
  • Known central nervous system (CNS) metastases.
  • Pregnant or breastfeeding

Who the study is looking for

  • Subject has histologically confirmed diagnosis of any one of the following cancers: (A) Synovial Sarcoma (SS), (B) MPNST, (C) Neuroblastoma, or (D) Osteosarcoma (OS).
  • Age:
    • (A) Synovial Sarcoma: 2 to 17 years (B) MPNST, Neuroblastoma and Osteosarcoma: 2 to 21 years
  • Body weight ≥ 10 kg
  • Must have previously received a systemic chemotherapy
  • Measurable disease prior to lymphodepletion according to RECIST v1.1 (or INCR, 2017 Neuroblastoma only).
  • HLA-A\*02 positive
  • Tumor shows MAGE-A4 expression confirmed by central laboratory.
  • Performance Status:
    • (A) Subjects ≥16: Eastern Cooperative Oncology Group (ECOG) 0 or 1 (B) Subjects 2 to 16: Lansky score ≥ 80
  • Subject has anticipated life expectancy of greater than 3 months in the opinion of the investigator.

Age in the registry: 2 years to 21 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (10)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
National Institutes of Health
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BethesdaUnited StatesRecruiting
Dana-Farber Cancer Institute
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BostonUnited StatesRecruiting
Cincinnati Children's Hospital Medical Center
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CincinnatiUnited StatesRecruiting
Duke University School of Medicine
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DurhamUnited StatesRecruiting
University of Wisconsin Cancer Center
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MadisonUnited StatesRecruiting
Memorial Sloan Kettering Kids
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New YorkUnited StatesRecruiting
Stanford University
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Palo AltoUnited StatesRecruiting
Children's Hospital of Philedephia
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PhiladelphiaUnited StatesRecruiting
Seattle Children's Hospital
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SeattleUnited StatesRecruiting
Washington University
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St LouisUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.