Novel BET Inhibitor PLX51107 for Steroid-Refractory Acute GVHD

- Age >= 18 years at the time of signing informed consent

- Steroid-refractory acute GVHD as defined as progression of acute (a)GvHD within 3-5 days of therapy onset with >= 2 mg/kg/day of prednisone equivalent OR failure to improve within 5-7 days of treatment initiation with > 1-2 mg/kg/day of prednisone equivalent OR incomplete response after more than 28 days of immunosuppressive treatment including steroids

- Recipients of ablative and reduced-intensity conditioning regimens

- Recipients of human leukocyte antigen (HLA)-matched related and unrelated, 1-allele mismatched, haploidentical, or umbilical cord blood donor grafts

- Prior lines of therapy for treatment of steroid-refractory acute GVHD are allowed. However, exposure to investigational therapies for the treatment of GVHD must be > 14 days or 5 half-lives (whichever is shorter) of first administration of study drug. For patients treated with ruxolitinib for the treatment of acute GVHD, ruxolitinib must be discontinued by at least one day prior to initiation of PLX51107

- Eastern Cooperative Oncology Group (ECOG) performance status =< 3

- Absolute neutrophil count >= 1.0 x 10^9/L for 3 consecutive days). Use of growth factor support is allowed

- Platelet count >= 50 x 10^9/L without transfusion support for 2 consecutive days

- Women of child-bearing potential must have a negative serum pregnancy test at Screening and must agree to use an effective form of contraception from the time of the negative pregnancy test up to 6 months after the last dose of study drug. Effective forms of contraception include abstinence, hormonal contraceptive in conjunction with a barrier method, or a double barrier method. Women of non-child-bearing potential may be included if they are either surgically sterile or have been postmenopausal for >= 1 year

- Fertile men must agree to use an effective method of birth control during the study and for up to 6 months after the last dose of study drug

- Prior exposure to a bromodomain inhibitor

- Evidence of chronic GVHD

- Evidence of active relapse of disease

- Exposure to other investigational or anti-cancer therapies (not for GVHD) within 28 days or 5 half-lives (whichever is shorter) of first administration of study drug

- Active, uncontrolled bacterial, fungal, or viral infection

- Known or suspected allergy to the study drug

- Clinically significant cardiac disease, defined as:

- Inability to take oral medication or significant nausea and vomiting, malabsorption, or significant small bowel resection that, in the opinion of the Investigator, would preclude adequate absorption

- Active thrombotic microangiopathy (TMA)

- Women who are either pregnant or breast feeding

- Measured or calculated (Cockcroft-Gault formula) creatinine clearance (CrCl) < 45 mL/min

- Prothrombin time or international normalized ratio > 1.5 x upper limit of normal (ULN)

- Activated partial thromboplastin time > 1.5 x ULN

- Requiring mechanical ventilation or vasopressor support

- Subject is participating in any other therapeutic clinical study (observational or registry studies are allowed)