Phase 2 Interstitial Lung Disease Trial, Recruiting NCT07323732 Sponsor: Memorial Sloan Kettering Cancer Center Condition: Interstitial Lung Disease
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Phase 2 Interstitial Lung Disease Trial, Recruiting

NCT07323732
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:

  • You must be 18 years old or older at the time you agree to take part.
  • You must have early-stage non-small cell lung cancer (Stage I or II), confirmed by a tissue sample where possible, or by scans and specialist agreement if a biopsy is too risky.
  • You must have been diagnosed with a lung scarring/inflammation condition called interstitial lung disease (ILD), either by a lung specialist, by scan results with a specific breathing test result, or because it developed from a connective tissue disease (such as rheumatoid arthritis, lupus, or similar conditions).
  • You must be well enough to carry out some daily activities (your doctor will assess this using a standard scale from 0 to 3).
  • If you are a woman who could become pregnant, you must either be confirmed post-menopausal (no periods for 12 months or more without another medical reason) or have a negative pregnancy test before joining.
  • You must be expected to live for at least 6 months.

Who may not be able to join:

  • You have had radiation treatment to the chest area before.
  • You have had a surgical procedure to remove an entire lung (pneumonectomy).
  • You have had a major operation (such as brain, chest, abdominal, or pelvic surgery) within the last 28 days.
  • You have a serious other illness that could prevent you from completing the radiation treatment or study procedures.
  • You have a known allergy or bad reaction to any of the study medications or their ingredients.
  • Your ILD has recently got much worse and required a hospital stay in the last 30 days.
  • You have poorly controlled heart rhythm problems that are not responding to treatment, or you have a pacemaker.
  • You are pregnant, breastfeeding, or able to have children and are not willing to use effective non-estrogen-based contraception (such as a condom plus a diaphragm, IUD, or certain other methods) from the start of the study until 30 days after the last dose of study medication.
  • You are currently taking or plan to take other experimental cancer treatments, chemotherapy, immunotherapy, or certain medications that affect the immune system (such as rituximab, tocilizumab, or similar drugs) at the same time as the study drug.

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 22 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: Narek Shaverdian, MD, Memorial Sloan Kettering Cancer Center

Phone: 631-212-6323

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
Registry
ClinicalTrials.gov
Start date
6 January 2026
Est. completion
6 January 2029

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Pneumonitis free survival

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: 22 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