Vimseltinib
DrugAdministered orally
Other names: DCC-3014
NCT Number: NCT06619561
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.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 2
City of Hope National Medical Center, Duarte, California, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
a. May have persistent active acute GVHD (aGVHD) and chronic GVHD (cGVHD) manifestations (overlap syndrome).
Exclusion criteria
Administered orally
Other names: DCC-3014
Time frame: Cycle 1 (28 Days)
DLTs assessed for each dose level.
Time frame: Baseline to Study Completion (Estimated up to 24 months)
AEs and SAEs assessed for each dose level.
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.
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.
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
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.
Time frame: Estimated up to 24 months
Cmax
Contact information is provided by the study sponsor or research team.
Deciphera Pharmaceuticals, LLC
Industry
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
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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