Phase 2 COPD Trial, Recruiting NCT06663722 Sponsor: University of Miami Condition: COPD
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Phase 2 COPD Trial, Recruiting

NCT06663722
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 have received a stem cell (bone marrow) transplant from a donor (not your own cells)
  • You are aged 12 or older
  • You have been diagnosed with chronic Graft-versus-Host Disease (cGVHD) — a condition where the donor cells attack your body — and need a new treatment after already trying at least 2 other treatments, or because steroids have stopped working, or because you cannot reduce your steroid dose without symptoms returning
  • Any other cGVHD treatments (apart from steroids and any transplant-related preventive medications) have been stopped before joining the study
  • You are reasonably active and able to care for yourself, based on a standard health scoring scale (scores 0–3 out of 4)
  • Your blood platelet count and white blood cell count are above certain minimum levels at the time of screening
  • Your liver enzyme levels are within an acceptable range (or are elevated only because of cGVHD)
  • Your steroid dose has been stable for at least 14 days before starting treatment
  • If you are sexually active and able to have children, you are willing to use contraception as required by the study

Who may not be able to join:

  • You are pregnant or breastfeeding
  • Your original cancer or condition that led to the transplant has come back (is actively relapsing)
  • You have a history of, or currently have, lung inflammation (scarring or irritation of lung tissue caused by illness or medication)
  • You are currently experiencing active bleeding in your stomach or intestines
  • Your kidneys, liver, lungs, or heart are not strong enough to safely handle the treatment process — for example, if your heart pumping strength is below 40% (confirm with trial site)
  • You have a history of muscle inflammation (myositis)
  • You have had your spleen removed
  • You have a history of pancreatitis (inflammation of the pancreas)
  • You have had another cancer diagnosed within the last 3 years, unless it was fully treated with the aim of curing it and the lead doctor approves
  • You have other serious or poorly controlled health conditions, or you are unable to follow the study requirements
  • You have HIV/AIDS, or currently have an active hepatitis B or hepatitis C infection
  • You have previously been treated with a specific type of drug that targets a protein called CSF-1R (confirm with trial site)
  • You have previously tried the main treatment used in this study (called ECP) and it did not work or you could not tolerate it
  • You are allergic or intolerant to certain medications used in the treatment process: methoxsalen, heparin, or citrate products
  • You do not have a lens in one or both eyes (aphakia), or you have a condition that makes your skin very sensitive to light (such as lupus, albinism, or porphyria)
  • You do not have reliable access to a vein or central line for regular intravenous (IV) treatment
  • Your health insurance has refused to cover the cost of the ECP treatment procedure

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 5 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: Trent P Wang, DO, University of Miami

Phone: +1 (305) 2436444

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
5 May 2025
Est. completion
5 May 2030

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Best Overall Response Rate (ORR)

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: 5 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