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NCT Number: NCT06619561

A Study to Evaluate Vimseltinib in Adults With Active Chronic Graft-Versus-Host Disease (cGVHD)

The purpose of this study is to determine if vimseltinib is safe, tolerable and works effectively to treat adults with active moderate to severe cGVHD. Participants will be treated with vimseltinib in 28-day treatment cycles for approximately 2 years.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

City of Hope National Medical Center, Duarte, California, United States

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Must be allogeneic hematopoietic stem cell transplant (HSCT) recipients with moderate to severe cGVHD requiring systemic immune suppression.

a. May have persistent active acute GVHD (aGVHD) and chronic GVHD (cGVHD) manifestations (overlap syndrome).

  • Participants with active cGVHD who have received and failed at least 2 prior lines of systemic therapy.
  • Stable dose of systemic corticosteroids is permitted but not required. If being taken, participants should be on a stable dose of corticosteroids for at least 2 weeks prior to starting study drug treatment.
  • Adequate organ and bone marrow functions.
  • Participants of reproductive potential agree to follow the contraception requirements.
  • Karnofsky Performance Scale (KPS) of ≥60.

Exclusion criteria

  • Has aGVHD without manifestations of cGVHD.
  • Prior use of colony-stimulating factor 1 receptor (CSF1R) inhibitor for cGVHD.
  • History or other evidence of severe illness, uncontrolled infection, or any other conditions that would make the participant unsuitable for the study. All wounds must be healed and free of infection or dehiscence.
  • History of malignancy except for:
  • Underlying malignancy for which the transplant was performed
  • Malignancy treated with curative intent and with no evidence of active disease present for more than 3 years prior to enrollment and felt to be at low risk for recurrence.
  • Malabsorption syndrome or other illness that could affect oral absorption.

Treatment and study plan

Vimseltinib

Drug

Administered orally

Other names: DCC-3014

Primary outcomes

  1. Number of Participants with Dose-Limiting Toxicities (DLTs)

    Time frame: Cycle 1 (28 Days)

    DLTs assessed for each dose level.

  2. Number of Participants with Adverse Event(s) (AEs) and Serious Adverse Event(s) (SAEs)

    Time frame: Baseline to Study Completion (Estimated up to 24 months)

    AEs and SAEs assessed for each dose level.

Secondary outcomes

  1. Objective Response Rate (ORR)

    Time frame: Baseline up to Cycle 7 Day 1 (Cycle = 28 days)

    ORR is percentage of participants achieving best overall response of complete response (CR) or partial response (PR) up to Cycle 7 Day 1 based on 2014 National Institutes of Health (NIH) cGVHD Criteria.

  2. Duration of Response (DOR)

    Time frame: First CR or PR until PD or Death due to Any Cause (Estimated up to 24 months)

    DOR for participants with CR or PR, defined as the time interval from the time of first CR or PR per 2014 NIH cGVHD Criteria, until PD, initiation of new systemic therapy for cGVHD, or death due to any cause, whichever occurs first.

  3. Organ-Specific Response

    Time frame: Baseline up to Cycle 7 Day 1 (Cycle = 28 days)

    Organ-specific response per 2014 NIH cGVHD Criteria up to Cycle 7 Day 1

  4. Failure-Free Survival (FFS)

    Time frame: Baseline to, whichever occurs first of, PD, Addition of Systemic Immune Suppressive Therapy, or Death due to Any Cause (Estimated up to 24 months)

    FFS is the time from first dose to progressive disease (PD) per 2014 NIH cGVHD Criteria, initiation of new systemic therapy for cGVHD, or death due to any cause, whichever occurs first.

  5. Pharmacokinetics (PK): Maximum Observed Plasma Concentration (Cmax)

    Time frame: Estimated up to 24 months

    Cmax

Study contacts

Contact information is provided by the study sponsor or research team.

Clinical Team

CONTACT

[email protected]

888-724-3274

Sponsors and collaborators

Lead sponsor

Deciphera Pharmaceuticals, LLC

Industry

Registry information

Official study title

A Phase 2, Open-label, Multicenter Study to Evaluate the Safety, Tolerability, PK, and Efficacy of Vimseltinib in Adults With Active Chronic GVHD After Failure of Prior Systemic Therapy

Important dates

Study start
2024
Primary completion
2029
Study completion
2029
First posted
Oct 1, 2024
Registry last updated
Dec 15, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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