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

RecruitingPhase 2

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

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
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.

About the study

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.

What is being tested

Sponsor: Deciphera Pharmaceuticals, LLC · Participants: 48 · Started: Nov 21, 2024

Contact the study team

Official record on ClinicalTrials.gov — NCT06619561

Locations in the U.S.

CaliforniaCity of Hope National Medical Center, Duarte
Ronald Regan UCLA Medical Center, Los Angeles
University of California Irvine Health, Orange
FloridaAdventHealth Orlando, Orlando
Moffitt Cancer Center, Tampa
GeorgiaEmory University Winship Cancer Institute, Atlanta
IllinoisUniversity of Illinois Medical Center - Hematology & Oncology, Chicago
KansasUniversity of Kansas Cancer Center-Westwood, Westwood
KentuckyUniversity of Kentucky Markey Cancer Center, Lexington
MassachusettsDana-Farber Cancer Institute, Boston
MichiganHenry Ford Cancer Institute, Detroit
MissouriWashington University School of Medicine - Siteman Cancer Center, St Louis
North CarolinaLevine Cancer Institute, Charlotte
Duke University Hospital, Durham
OhioOncology Hematology Care Clinical Trials, LLC, Cincinnati
Cleveland Clinic, Cleveland
The Ohio State University Comprehensive Cancer Center, Columbus
OregonOregon Health and Science University, Portland
PennsylvaniaUPMC Hillman Cancer Center, Pittsburgh
South DakotaAvera Cancer Institute, Sioux Falls
TennesseeTristar Bone Marrow Transplant, Nashville
Vanderbilt-Ingram Cancer Center, Nashville
TexasSt. David's South Austin Medical Center, Austin
UT Southwestern Medical Center, Dallas
UtahIntermountain Health, Salt Lake City
VirginiaVirginia Commonwealth University, Richmond

Conditions

From ClinicalTrials.gov, data retrieved Sep 29, 2026. Each study sets its own eligibility; the study team decides who can join.