This is an open-label, Phase 2 study designed to evaluate the safety and efficacy of belumosudil and rituximab as primary treatment of cGVHD.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
25
200mg PO QD x 24 cycles (28-day cycle)
375mg/m2 IV Q1 week x 4 weeks, then Q3 months x4 doses
Northside Hospital
Atlanta, Georgia, United States
RECRUITINGNumber of patients who achieve partial and complete responses after treatment
Time frame: 2 years
Length of time patients remain on corticosteroid treatment
Time frame: 2 years
Number of patients who had treatment-related adverse events using CTCAE v5
Time frame: 2 years
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.