Phase 2 COPD Trial, Recruiting NCT07124078 Sponsor: Incyte Corporation Condition: COPD
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Phase 2 COPD Trial, Recruiting

NCT07124078
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:

  • Children and teenagers aged 2 years old up to (but not including) 18 years old at the time of signing the consent forms.
  • People who have active, moderate to severe chronic graft-versus-host disease (a condition that can occur after a stem cell transplant) that requires treatment with medicines that suppress the immune system.
  • People whose chronic graft-versus-host disease has not responded to treatment or has come back, and who have already been treated with at least 2 different systemic (whole-body) treatment courses, including steroids and a medicine called ruxolitinib.
  • People who are already taking steroid medicines by mouth or injection, provided the dose has been stable for at least 2 weeks before the trial starts. Steroids applied to the skin or taken by inhaler are also permitted.
  • People who are willing to be treated with one of a specific list of medicines at the start of the trial, which includes cyclosporine, tacrolimus, extracorporeal photopheresis (ECP), mycophenolate mofetil (MMF), everolimus, sirolimus, rituximab, imatinib, methotrexate, or ibrutinib (confirm with trial site which options apply).
  • People who have previously received a stem cell transplant from a donor (related or unrelated, with any level of tissue matching), using any type of stem cell source, and with any type of pre-transplant preparation regimen.

Who may not be able to join:

  • People who have had more than one prior donor stem cell transplant. (A previous transplant using the person's own stem cells is permitted.)
  • People whose original blood disease has come back after the transplant, or who have received treatment specifically because the disease returned, including certain donor cell infusions given to treat relapse.
  • People who have started taking cyclosporine, tacrolimus, or similar medicines (called CNIs or mTOR inhibitors) within 2 weeks before the trial start date.
  • People with severely reduced kidney function or who are on dialysis due to kidney failure.
  • People with significant liver problems (based on specific blood test results), unless those liver problems are caused by graft-versus-host disease affecting the liver.
  • People with a history of inflammation of the pancreas (either short-term or long-term).
  • People who currently have active and symptomatic muscle inflammation (myositis).
  • Female adolescents who are pregnant or breastfeeding.

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 15 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: Incyte Medical Monitor, Incyte Corporation

Phone: 1.855.463.3463

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
Incyte Corporation
Registry
ClinicalTrials.gov
Start date
20 May 2026
Est. completion
31 January 2029

Where this trial is recruiting

🇧🇪 Belgium 🇩🇪 Germany 🇮🇹 Italy 🇪🇸 Spain 🇬🇧 United Kingdom 🇺🇸 United States

Primary endpoints

Objective Response (OR) at 6 months

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: 15 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