Phase 2 Lung Cancer Trial, Recruiting NCT04210492 Sponsor: Yale University Condition: Lung Cancer
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Phase 2 Lung Cancer Trial, Recruiting

NCT04210492
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People with a lung tumor that is 5 cm or smaller and located in a central part of the lung, meaning the tumor is near major airways, large blood vessels, the food pipe (esophagus), or the heart (confirm exact location details with trial site)
  • People with more than one lung tumor at the same time may also be considered, as long as at least one tumor meets the size and location requirements above
  • People who are generally well enough to carry out daily activities with little or no assistance (rated on a standard medical scale as 0, 1, or 2 out of 4)
  • People aged 18 or older
  • People who are willing and able to sign a consent form for this study

Who may not be able to join:

  • People who have previously had radiation treatment near the target tumor area, where earlier radiation reached certain high dose levels to nearby body structures such as the spinal cord, nerve bundles in the shoulder area (brachial plexus), parts of the digestive tract, the brainstem, or a large portion of the lung (confirm specific dose thresholds with trial site)
  • People who currently have an active infection in the body, lungs, or around the heart
  • People who have a condition causing ongoing inflammation or significant scarring of the lung tissue
  • People who are currently pregnant or breastfeeding
  • People who have any other medical condition that, in the opinion of the trial doctor, would make participation unsafe or unsuitable

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 26 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Henry S. Park, MD, MPH, Yale University

Phone: 203-200-2100

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Registry
ClinicalTrials.gov
Start date
26 August 2020
Est. completion
1 January 2030

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Safety of the stereotactic body radiotherapy regimen (SBRT); local control (LC) of 3-fraction stereotactic body radiotherapy

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov