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NCT03033303 · ClinicalTrials.gov registry record · Phase 2

A Study of the Effect of Hu3F8/GM-CSF Immunotherapy Plus Isotretinoin in Patients in First Remission of High-Risk Neuroblastoma

A Phase 2 study, sponsored by Memorial Sloan Kettering Cancer Center.

Completed
Registry status
Phase 2
Development phase
59
Enrollment target

NCT03033303: Completed Phase 2 study, sponsored by Memorial Sloan Kettering Cancer Center.

NCT03033303 is a Phase 2 study that has completed, run by Memorial Sloan Kettering Cancer Center. The registered enrollment target is 59 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (56% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03033303, a Phase 2 study, has completed, sponsored by Memorial Sloan Kettering Cancer Center.

COMPLETED
Registry status
Phase 2
Development phase
59 participants
Enrollment target

Study Summary

The purpose of this study is to test see the combined effects of the study drug called Humanized 3F8 (Hu3F8) when used with granulocyte-macrophage colony stimulating factor (GM-CSF). Hu3F8 plus GM-CSF could prevent your neuroblastoma from growing, but it could also cause side effects.

Primary Outcome

Patients are considered a response failure under this protocol if progressive disease is evident before two years. Deaths from toxicity attributable to protocol treatment will be counted as events. Patients who withdraw or are lost to followup before two years will be considered as progressions.

Interventions

  • DRUG Isotretinoin
  • DRUG GM-CSF
  • BIOLOGICAL Hu3F8

Trial Details

FieldValue
Enrollment Target 59 participants
Start Date 2017-01-23
Est. Completion 2025-09-29
Phase Phase 2
Memorial Sloan Kettering Cancer Center

1,884 total trials

What the finished NCT03033303 record still lists

NCT03033303 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 59 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (56% lower).

The record links to 0 conditions, and to 3 interventions - of which Isotretinoin is the first listed.

NCT03033303 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03033303 about?

NCT03033303 is a clinical study titled "A Study of the Effect of Hu3F8/GM-CSF Immunotherapy Plus Isotretinoin in Patients in First Remission of High-Risk Neuroblastoma". The purpose of this study is to test see the combined effects of the study drug called Humanized 3F8 (Hu3F8) when used with granulocyte-macrophage colony stimulating factor (GM-CSF). Hu3F8 plus GM-CSF could prevent your neuroblastoma from growing, but it could also cause side effects.

What is the current status of trial NCT03033303?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 59 participants. The study started on 2017-01-23. Estimated completion is 2025-09-29.

What interventions are being tested in trial NCT03033303?

The interventions under investigation include: Isotretinoin (DRUG), GM-CSF (DRUG), Hu3F8 (BIOLOGICAL).

Who is sponsoring clinical trial NCT03033303?

This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 1,884 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03033303's enrollment target sits among peer trials

59 1133rd of 2000 higher than 866 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03033303, the US trial registry maintained by the National Library of Medicine. NCT03033303 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.