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NCT04376502 · ClinicalTrials.gov registry record · NA

Immune Checkpoint Inhibitor and MR-guided SBRT for Limited Progressive Metastatic Carcinoma.

A NA study, sponsored by Baptist Health South Florida.

Terminated
Registry status
NA
Development phase
12
Enrollment target

NCT04376502: Clinical Trial NA study, sponsored by Baptist Health South Florida.

NCT04376502 is a NA study that was terminated before completion, run by Baptist Health South Florida. The registered enrollment target is 12 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04376502, a NA study, was terminated before completion, sponsored by Baptist Health South Florida.

TERMINATED
Registry status
NA
Development phase
12 participants
Enrollment target

Study Summary

This is an open label single arm phase 2 clinical trial in patients with metastatic solid malignancy of any histology who have previously experienced limited progression in at least 1 and up to 5 lesions while on immune checkpoint inhibitors monotherapy.

Primary Outcome

ORR is defined as the percent of participants who have a partial response (PR) or complete response (CR) to therapy of non-irradiated lesions according to Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST v1.1) criteria assessed on CT imaging. CR is defined as the disappearance of all target and non-target lesions. PR is defined as at least a 30% decrease from baseline in the sum of the longest diameters of target lesions AND for non-target lesions, no progression of existing lesi

Interventions

  • RADIATION Radiation Therapy

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2020-04-08
Est. Completion 2023-10-04
Phase NA
Baptist Health South Florida

40 total trials

Why NCT04376502 stopped before completion

NCT04376502 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 1 intervention - of which Radiation Therapy is the first listed.

NCT04376502 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04376502 about?

NCT04376502 is a clinical study titled "Immune Checkpoint Inhibitor and MR-guided SBRT for Limited Progressive Metastatic Carcinoma.". This is an open label single arm phase 2 clinical trial in patients with metastatic solid malignancy of any histology who have previously experienced limited progression in at least 1 and up to 5 lesions while on immune checkpoint inhibitors monotherapy.

What is the current status of trial NCT04376502?

This trial is currently terminated. It is a NA study. The enrollment target is 12 participants. The study started on 2020-04-08. Estimated completion is 2023-10-04.

What interventions are being tested in trial NCT04376502?

The interventions under investigation include: Radiation Therapy (RADIATION).

Who is sponsoring clinical trial NCT04376502?

This trial is sponsored by Baptist Health South Florida, which has 40 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04376502's enrollment target sits among peer trials

12 1913th of 2000 higher than 74 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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 NCT04376502, the US trial registry maintained by the National Library of Medicine. NCT04376502 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.