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NCT07293247 · ClinicalTrials.gov registry record · Phase 2

A Study of Targeted Post-Surgery Radiation Therapy for Non-Small Cell Lung Cancer With Remaining Lymph Node Cancer After Treatment

A Phase 2 study, sponsored by Alliance for Clinical Trials in Oncology.

Recruiting
Registry status
Phase 2
Development phase
164
Enrollment target

NCT07293247: Recruiting Phase 2 study, sponsored by Alliance for Clinical Trials in Oncology.

NCT07293247 is a Phase 2 study that is actively recruiting participants, run by Alliance for Clinical Trials in Oncology. The registered enrollment target is 164 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (23% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07293247, a Phase 2 study, is actively recruiting participants, sponsored by Alliance for Clinical Trials in Oncology.

RECRUITING
Registry status
Phase 2
Development phase
164 participants
Enrollment target

Study Summary

This phase II trial compares the effect of intensity-modulated post-operative radiation therapy (I²-PORT) followed by standard of care therapy (chemotherapy or immunotherapy) to standard of care therapy alone in treating patients with non-small cell lung cancer (NSCLC) who have remaining lymph node cancer after surgery. Radiation therapy uses high-energy X-rays, particles, or radioactive seeds to kill cancer cells and shrink tumors. Intensity-modulated radiation therapy is a type of 3-dimensional radiation therapy that uses computer-generated images to show the size and shape of the tumor. Thin beams of radiation of different intensities are aimed at the tumor from many angles. This type of radiation therapy reduces the damage to healthy tissue near the tumor. Chemotherapy drugs work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Immunotherapy may induce changes in the body's immune system and may interfere with the ability of tumor cells to grow and spread. Adding I²-PORT radiation therapy to standard therapy may be more effective than standard therapy alone in reducing the risk of cancer returning in those who have undergone surgery for NSCLC.

Primary Outcome

DFS will be analyzed using the Kaplan-Meier methodology and compared between Arm 2 and Arm 1 using a log-rank test stratified by randomization factors. The median DFS for each treatment group will be estimated, and its 80% and 90% confidence intervals will be calculated using the Kaplan-Meier estimator. Additionally, the 24-month DFS rate for each treatment arm, along with its confidence intervals, will be calculated.

Interventions

  • PROCEDURE Computed Tomography
  • PROCEDURE Magnetic Resonance Imaging
  • DRUG Chemotherapy
  • RADIATION Intensity-Modulated Radiation Therapy
  • OTHER Immunotherapy

Trial Details

FieldValue
Enrollment Target 164 participants
Start Date 2026-07-14
Est. Completion 2032-03-01
Phase Phase 2

What NCT07293247 shows while recruiting

NCT07293247 is an interventional study that assigns participants to a tested intervention. The registered 164 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (23% higher).

The record links to 0 conditions, and to 5 interventions - of which Computed Tomography is the first listed.

NCT07293247 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07293247 about?

NCT07293247 is a clinical study titled "A Study of Targeted Post-Surgery Radiation Therapy for Non-Small Cell Lung Cancer With Remaining Lymph Node Cancer After Treatment". This phase II trial compares the effect of intensity-modulated post-operative radiation therapy (I²-PORT) followed by standard of care therapy (chemotherapy or immunotherapy) to standard of care therapy alone in treating patients with non-small cell lung cancer (NSCLC) who have remaining lymph node ...

What is the current status of trial NCT07293247?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 164 participants. The study started on 2026-07-14. Estimated completion is 2032-03-01.

What interventions are being tested in trial NCT07293247?

The interventions under investigation include: Computed Tomography (PROCEDURE), Magnetic Resonance Imaging (PROCEDURE), Chemotherapy (DRUG), Intensity-Modulated Radiation Therapy (RADIATION), Immunotherapy (OTHER).

Who is sponsoring clinical trial NCT07293247?

This trial is sponsored by Alliance for Clinical Trials in Oncology, which has 446 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07293247's enrollment target sits among peer trials

164 413th of 2000 higher than 1,583 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 NCT07293247, the US trial registry maintained by the National Library of Medicine. NCT07293247 (mid enrollment · none site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.