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NCT07210632 · ClinicalTrials.gov registry record · Early Phase 1

Window Trial of Fluorescently Labeled Nivolumab-IRDye800 (Nivo800) in High Grade Glioma (HGG)

A Early Phase 1 study, sponsored by Eben Rosenthal.

Recruiting
Registry status
Early Phase 1
Development phase
38
Enrollment target

NCT07210632: Recruiting Early Phase 1 study, sponsored by Eben Rosenthal.

NCT07210632 is a Early Phase 1 study that is actively recruiting participants, run by Eben Rosenthal. The registered enrollment target is 38 participants, below the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (28% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07210632, a Early Phase 1 study, is actively recruiting participants, sponsored by Eben Rosenthal.

RECRUITING
Registry status
Early Phase 1
Development phase
38 participants
Enrollment target

Study Summary

High-grade gliomas (HGGs) are among the most aggressive and treatment-resistant brain tumors. Immunotherapy with checkpoint inhibitors like nivolumab has shown promise, but its efficacy remains variable and poorly understood in this patient population. This clinical trial investigates a novel imaging-enabled formulation of nivolumab-IRDye800 (nivo800) which incorporates a near-infrared (NIR) fluorescent dye to enable real-time visualization of drug distribution within tumor tissue.

Primary Outcome

As defined by the number of Grade ≥ 2 Adverse Events (AEs) determined that are clinically significant and considered definitely or probably related to nivo800. Safety data will be summarized by grade, severity, and type.

Interventions

  • DRUG Nivolumab
  • DRUG Nivolumab-IRDye800

Trial Details

FieldValue
Enrollment Target 38 participants
Start Date 2026-03-27
Est. Completion 2031-03-30
Phase Early Phase 1
Eben Rosenthal

8 total trials

What NCT07210632 shows while recruiting

NCT07210632 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 38 participants, a relatively small participant target, below the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (28% lower).

The record links to 0 conditions, and to 2 interventions - of which Nivolumab is the first listed.

NCT07210632 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07210632 about?

NCT07210632 is a clinical study titled "Window Trial of Fluorescently Labeled Nivolumab-IRDye800 (Nivo800) in High Grade Glioma (HGG)". High-grade gliomas (HGGs) are among the most aggressive and treatment-resistant brain tumors. Immunotherapy with checkpoint inhibitors like nivolumab has shown promise, but its efficacy remains variable and poorly understood in this patient population. This clinical trial investigates a novel imagin...

What is the current status of trial NCT07210632?

This trial is currently recruiting. It is a Early Phase 1 study. The enrollment target is 38 participants. The study started on 2026-03-27. Estimated completion is 2031-03-30.

What interventions are being tested in trial NCT07210632?

The interventions under investigation include: Nivolumab (DRUG), Nivolumab-IRDye800 (DRUG).

Who is sponsoring clinical trial NCT07210632?

This trial is sponsored by Eben Rosenthal, which has 8 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07210632's enrollment target sits among peer trials

38 699th of 2000 higher than 1,299 of 2,000 other Early Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Early Phase 1 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 NCT07210632, the US trial registry maintained by the National Library of Medicine. NCT07210632 (small enrollment · none site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.