Phase 2 COPD Trial, Recruiting NCT06619561 Sponsor: Deciphera Pharmaceuticals, LLC Condition: COPD
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Phase 2 COPD Trial, Recruiting

NCT06619561
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 have received a stem cell transplant from a donor and developed moderate to severe chronic graft-versus-host disease (cGVHD) — a condition where the donor cells attack the recipient's body — that requires treatment with immune-suppressing medicines.
  • People who have both an ongoing acute (sudden-onset) form and a chronic form of graft-versus-host disease at the same time (sometimes called overlap syndrome) may also be considered.
  • People with active chronic graft-versus-host disease who have already tried and not responded to at least 2 different systemic (whole-body) treatments.
  • People who are taking corticosteroids (steroid medicines) at a stable dose for at least 2 weeks before starting the study treatment, or people who are not taking corticosteroids at all.
  • People whose heart, liver, kidneys, and bone marrow are functioning at an adequate level.
  • People of reproductive potential who agree to follow the contraception requirements set out by the trial.
  • People who score 60 or above on the Karnofsky Performance Scale, a measure of a person's ability to carry out daily activities (confirm with trial site).

Who may not be able to join:

  • People who have only the acute form of graft-versus-host disease, with no signs of the chronic form.
  • People who have previously been treated with a type of medicine called a CSF1R inhibitor for chronic graft-versus-host disease.
  • People with a serious uncontrolled illness, uncontrolled infection, or any other health condition that the trial site determines would make participation unsuitable — all wounds must also be fully healed and free of infection.
  • People with a history of cancer, except for the original cancer that led to the stem cell transplant, or a previous cancer that was treated with the intention of a cure, shows no signs of returning, and occurred more than 3 years before joining the trial.
  • People with a condition that affects the body's ability to absorb medicines taken by mouth, such as malabsorption syndrome.

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: Clinical Team, Deciphera Pharmaceuticals, LLC

Phone: 888-724-3274

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
Deciphera Pharmaceuticals, LLC
Registry
ClinicalTrials.gov
Start date
21 November 2024
Est. completion
1 October 2029

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Number of Participants with Dose-Limiting Toxicities (DLTs); Number of Participants with Adverse Event(s) (AEs) and Serious Adverse Event(s) (SAEs)

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