Phase 2 COPD Trial, Recruiting NCT06843408 Sponsor: Incyte Corporation Condition: COPD
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Phase 2 COPD Trial, Recruiting

NCT06843408
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 who are at least 12 years old at the time of signing the consent form.
  • People who are able to understand and are willing to sign a written consent form; for those aged 12 to 17, a parent or guardian must also provide consent.
  • People of Chinese background who have received a stem cell transplant from a donor and who have chronic graft-versus-host disease (cGVHD) — a condition where the donated cells attack the body — that is active, not responding to treatment, or has come back, and that requires ongoing immune-suppressing medication after trying steroids and at least one other treatment.
  • People who have both an ongoing acute form and a chronic form of graft-versus-host disease at the same time (sometimes called "overlap syndrome").
  • People who have a general health and functioning score of 60 or above on the relevant scale for their age group, indicating they are able to carry out some daily activities (confirm with trial site).
  • People whose blood counts and organ function — including white blood cells, platelets, liver, and kidney measures — fall within the acceptable ranges tested in the 14 days before starting the study treatment.
  • People who are already taking steroid medications, as long as the dose has been stable for at least 2 weeks before starting the study treatment.
  • People who are already taking certain immune-suppressing medications (CNIs or mTOR inhibitors), as long as the dose has been stable and within the appropriate range for at least 2 weeks before starting the study treatment.
  • People who are willing to use appropriate contraception and avoid pregnancy or fathering children during the study and for a set period after the last dose of study treatment.

Who may not be able to join:

  • People who have the acute form of graft-versus-host disease only, with no signs of the chronic form.
  • People who show any signs that their original cancer has returned, or who have developed a transplant-related lymph gland disease, at the time of screening.
  • People with a history of acute or chronic inflammation of the pancreas (pancreatitis).
  • People who currently have active, symptomatic muscle inflammation (myositis).
  • People with a history of serious illness, an uncontrolled infection, an allergy to ingredients in the study drug, or any other condition that the study doctor believes would make participation unsafe.
  • People who are HIV positive.
  • People with a history of active or latent tuberculosis (TB), recent close contact with someone who has active TB, or a positive TB blood test at screening.
  • People with active hepatitis B or hepatitis C infection requiring treatment, or those at risk of hepatitis B reactivation based on specific blood test results at screening.
  • People diagnosed with another cancer (other than the one for which the transplant was done) within the past 3 years, unless it was fully treated with the intent to cure and approved by the study's medical oversight team.
  • People who are pregnant or breastfeeding.
  • People who have previously received a treatment that targets a specific protein called CSF-1R.
  • People who have used any cGVHD treatment other than steroids, CNIs, or mTOR inhibitors within 2 weeks (or 5 half-lives of that medication, whichever is shorter) before starting the study treatment.
  • People who have taken part in another experimental treatment study within 28 days before starting the study treatment.
  • People who are currently taking part in any other treatment-based clinical 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 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: 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
25 June 2025
Est. completion
3 July 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Number of participants with Treatment-emergent Adverse Events (TEAEs); Objective Response in the First 6 Cycles

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