Phase 2 COPD Trial, Recruiting NCT07012304 Sponsor: Yujun DONG Condition: COPD
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Phase 2 COPD Trial, Recruiting

NCT07012304
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 aged 18 or older who have voluntarily agreed to participate by signing a consent form
  • People who have previously received a stem cell transplant from a donor (using bone marrow, blood stem cells, or umbilical cord blood), using any of the standard transplant preparation methods
  • People whose transplant has successfully taken hold, shown by blood count levels meeting specific thresholds, without needing growth factor support or blood transfusions in the 7 days before screening
  • People who have been diagnosed with moderate-to-severe chronic graft-versus-host disease (a condition where donor cells affect the recipient's body) based on 2014 NIH guidelines
  • People who have already tried 2 to 5 previous systemic treatments for their chronic graft-versus-host disease but still have active disease
  • People with a general health/activity score of 0–2 on a standard medical scale (meaning able to carry out daily activities with at most some limitations)
  • People who are able to swallow tablets
  • People who are taking certain other immune-suppressing medications that do not interact with the trial drug

Who may not be able to join:

  • People whose original cancer or blood disease has come back, or whose transplanted cells have not fully taken over from their own
  • People currently using other medications in a similar drug class (JAK inhibitors), mesenchymal stem cells, or a drug called belumosudil — though people who stopped these treatments more than 8 weeks ago, or who stopped JAK inhibitors due to side effects, may still be considered (confirm with trial site)
  • People with severe lung involvement from their graft-versus-host disease, based on specific breathing test results or symptom scores
  • People who have developed a condition called post-transplant lymphoproliferative disease (an abnormal growth of immune cells after transplant)
  • People with certain significant health abnormalities, including poorly controlled high blood pressure despite medication, or liver or kidney function levels outside acceptable ranges on blood tests
  • People who have had a major heart event (such as a heart attack or stroke) within the past 6 months
  • People who have a heart rhythm problem that requires treatment at the time of screening
  • People with digestive system conditions that could prevent the body from properly absorbing the trial medication
  • People who had surgery within 4 weeks before screening and have not fully recovered
  • People with an active or uncontrolled infection (bacterial, viral, fungal, or parasitic) that currently requires treatment
  • People with active tuberculosis within the past 6 months
  • People with epilepsy, or who are taking medications that affect mood, mental state, or cause sedation
  • People who are pregnant, breastfeeding, or unwilling to use contraception during the trial and for 4 weeks after it ends
  • People who have had a cancer diagnosis within the past 5 years, other than the condition that led to their transplant
  • People currently taking blood-thinning or anti-clotting medications, with the exception of a specific type of heparin (low-molecular-weight heparin)
  • People who have used herbal medicines within 1 week before enrolling
  • People known to have an allergy or sensitivity to the trial drug or any of its ingredients
  • People who have participated in another clinical trial within the past 4 weeks, or within a longer period based on the previous trial drug (whichever is longer)
  • People considered unsuitable for the trial by the medical team running the study

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 21 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.

GP referral letter

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Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Yujun DONG
Registry
ClinicalTrials.gov
Start date
30 June 2025
Est. completion
28 February 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Overall Response Rate (ORR) at Week 24

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: 21 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