Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

New imaging method could spot hidden cancers

NCT ID NCT02307630

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

7 people

The number who actually took part.

Started

Nov 2014

Expected to finish

Nov 2026

An estimate. End dates often move.

Lead sponsor

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

3 to 90 years

Sex

Anyone

Healthy volunteers

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

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.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Ewing sarcoma are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

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

  • Memorial Sloan Kettering Cancer Center

    New York, New York, 10065, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.