Recruiting
Phase 2

Vimseltinib

Sponsor:

Deciphera Pharmaceuticals, LLC

Code:

NCT06619561

Conditions

Chronic Graft-Versus-Host Disease (cGVHD)

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Vimseltinib

Study Details

Brief summary:

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.

Conditions

Chronic Graft-Versus-Host Disease (cGVHD)

Study ID

NCT06619561

Start date

Nov 21, 2024

Status verified date

Dec, 2025

Completion date

Oct, 2029

Anticipated

Primary completion date

Oct, 2029

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

1. 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).
2. Participants with active cGVHD who have received and failed at least 2 prior lines of systemic therapy.
3. 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.
4. Adequate organ and bone marrow functions.
5. Participants of reproductive potential agree to follow the contraception requirements.
6. Karnofsky Performance Scale (KPS) of ≥60.

Exclusion Criteria:

1. Has aGVHD without manifestations of cGVHD.
2. Prior use of colony-stimulating factor 1 receptor (CSF1R) inhibitor for cGVHD.
3. 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.
4. History of malignancy except for:

1. Underlying malignancy for which the transplant was performed
2. 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.
5. Malabsorption syndrome or other illness that could affect oral absorption.

Study Design

Enrollment

48 participants

Anticipated

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Vimseltinib

Escalating doses of vimseltinib in 28 day cycles.

Interventions

Vimseltinib

Administered orally

Primary outcome measure

  • Number of Participants with Dose-Limiting Toxicities (DLTs) [ Time Frame: Cycle 1 (28 Days) ]
  • 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) ]

Central Contacts and Locations

Central contacts

Locations

City of Hope National Medical Center

Recruiting

Duarte, California, United States, 91010

Ronald Regan UCLA Medical Center

Recruiting

Los Angeles, California, United States, 90095

University of California Irvine Health

Recruiting

Orange, California, United States, 92868-3201

AdventHealth Orlando

Recruiting

Orlando, Florida, United States, 32804

Moffitt Cancer Center

Recruiting

Tampa, Florida, United States, 33612

Emory University Winship Cancer Institute

Recruiting

Atlanta, Georgia, United States, 30322

University of Illinois Medical Center - Hematology & Oncology

Recruiting

Chicago, Illinois, United States, 60612

University of Kansas Cancer Center-Westwood

Recruiting

Westwood, Kansas, United States, 66205

University of Kentucky Markey Cancer Center

Recruiting

Lexington, Kentucky, United States, 40536

Dana-Farber Cancer Institute

Recruiting

Boston, Massachusetts, United States, 02215

Henry Ford Cancer Institute

Recruiting

Detroit, Michigan, United States, 48202

Washington University School of Medicine - Siteman Cancer Center

Recruiting

St Louis, Missouri, United States, 63108

Levine Cancer Institute

Recruiting

Charlotte, North Carolina, United States, 28204

Duke University Hospital

Recruiting

Durham, North Carolina, United States, 27705

Oncology Hematology Care Clinical Trials, LLC

Recruiting

Cincinnati, Ohio, United States, 45242

Cleveland Clinic

Recruiting

Cleveland, Ohio, United States, 44195

The Ohio State University Comprehensive Cancer Center

Recruiting

Columbus, Ohio, United States, 43210

Oregon Health and Science University

Recruiting

Portland, Oregon, United States, 97239

UPMC Hillman Cancer Center

Recruiting

Pittsburgh, Pennsylvania, United States, 15232

Avera Cancer Institute

Recruiting

Sioux Falls, South Dakota, United States, 57105

Tristar Bone Marrow Transplant

Recruiting

Nashville, Tennessee, United States, 37203

Vanderbilt-Ingram Cancer Center

Recruiting

Nashville, Tennessee, United States, 37232

St. David's South Austin Medical Center

Recruiting

Austin, Texas, United States, 78704

UT Southwestern Medical Center

Recruiting

Dallas, Texas, United States, 75390

Intermountain Health

Recruiting

Salt Lake City, Utah, United States, 84143

Virginia Commonwealth University

Recruiting

Richmond, Virginia, United States, 23298

More Information

Sponsor

Deciphera Pharmaceuticals, LLC

Last update posted

Dec 15, 2025

Last verified

Dec, 2025

Keywords

  • Allogeneic hematopoietic stem cell transplant (HSCT)
  • Graft-Versus-Host Disease
  • GVHD
  • cGVHD
  • Graft versus host disease
  • Immune System Diseases
  • Organizing Pneumonia
  • Bronchiolitis Obliterans
  • Bronchiolitis
  • Bronchial Diseases
  • Respiratory Tract Diseases
  • Lung Diseases, Obstructive
  • Lung Diseases
  • Bronchiolitis Obliterans Syndrome
  • Graft vs Host Disease
  • Sclerosis
  • Fibrosis
  • Hematopoietic stem cell transplantation
  • Liver diseases

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Deciphera Pharmaceuticals, LLC on 2025-12-15.