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

Deciphera Pharmaceuticals, LLC

Status and phase: Enrolling; Phase 2

Conditions: Chronic Graft-Versus-Host Disease (cGVHD)

Treatments: Drug: Vimseltinib

Study type: Interventional

Funder types: Industry

Identifiers

NCT06619561

DCC-3014-02-001

Details and patient eligibility

About

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.

Enrollment: 36 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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 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.

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.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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36 participants in 1 patient group

Vimseltinib

Experimental group

Description:

Escalating doses of vimseltinib in 28 day cycles.

Treatment:

Drug: Vimseltinib