New imaging method could spot hidden cancers
NCT ID NCT02307630
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This pilot study is testing a radioactive antibody called 124I-Humanized 3F8 to see how it travels through the body and attaches to tumors in people with melanoma, neuroblastoma, or sarcoma. Seven participants will receive the antibody and then have PET/CT scans at several time points. The goal is to learn about the antibody's distribution and how long it stays in the body, which could improve cancer imaging in the future.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- 124I-Humanized 3F8 (a radioactive antibody)
- What this could lead to
- If successful, this could lead to better PET scans for detecting certain solid tumors, helping doctors see where the cancer is more clearly.
- What could go wrong
- This is a very small pilot study with only 7 participants, so results may not apply to everyone. It is designed to test imaging, not to treat or cure cancer, so no direct benefit is expected.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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7 people
The number who actually took part.
- Started
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Nov 2014
- Expected to finish
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Nov 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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3 to 90 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients with the diagnosis of neuroblastoma must meet both of the following criteria: * Diagnosis confirmed by histological assessment by MSKCC Department of pathology or by the presence of BM metastases PLUS elevated urinary catecholamines * Relapsed or refractory stage 4 disease or relapsed or refractory stage MYCN-amplified 2B or 3 disease. * Patients with tumors other than neuroblastoma must meet both the following criteria: * Have one of the following diagnoses (these tumors are known to express GD2 on cell surface): * Melanoma * Osteogenic sarcoma * Leiomyosarcoma * Ewing sarcoma * Liposarcoma * Fibrosarcoma * Malignant fibrous histiocytoma * Spindle cell sarcoma * Small cell lung cancer * Medulloblastoma metastatic to extracranial sites * Paraganglioma * Have refractory or relapsed or metastatic disease * Patients with solid tumors with diagnoses OTHER than neuroblastoma or those listed above will be eligible if they meet both of the following criteria: * Immunohistochemical demonstration of GD2 expression on cell surface (Tumor assessment by immunohistochemistry is required for this group of patients) * Have refractory or relapsed disease or metastatic disease. All patients must have measurable or evaluable disease * Age 3-90 years * Prior treatment with anti-GD2 monoclonal antibody is permitted only if human anti-human antibody titer is ≤1300 assay developed by Dr. Nai-Kong Cheung. * Negative serum pregnancy test in women of childbearing potential * Women of child-bearing potential must be willing to practice an effective method of birth control while on study * Signed informed consent indicating awareness of the investigational nature of this study. Exclusion Criteria: * Existing major organ dysfunction \> grade 2, with the exception of myelosuppression (neutrophil count \> or = 500/μl and platelet count \> or = 25,000/μl are acceptable) and hearing loss. * Acute life threatening infection * Requirement for sedation for PET/CT scans * Pregnant women or women who are breast-feeding. * Inability to comply with protocol requirements. * Hypersensitivity to potassium iodide or Lugols products * Prior development of positive human antimouse antibody response (HAMA) or human antihuman antibody response (HAHA) * Positive human anti-hu3F8 antibody titer.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Memorial Sloan Kettering Cancer Center
New York, New York, 10065, United States
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