A Study to Compare T-Guard vs Ruxolitinib for Treatment of Steroid-Refractory Acute Graft-vs-Host Disease (BMT CTN 2002)

Xenikos

Status and phase: Terminated; Phase 3

Conditions: Steroid-Refractory Acute Graft Versus Host Disease

Treatments: Drug: Ruxolitinib; Drug: T-Guard

Study type: Interventional

Funder types: Other; NETWORK; Industry; NIH

Identifiers

NCT04934670

2021-000343-53 (EudraCT Number)

5U24HL138660-02 (U.S. NIH Grant/Contract)

U24HL138660 (U.S. NIH Grant/Contract)

BMT CTN 2002

U10HL069294 (U.S. NIH Grant/Contract)

XEN-TG-005 (Other Identifier)

Details and patient eligibility

About

This is an open-label, randomized, Phase 3, multicenter trial, which has been designed to compare the efficacy and safety of T-Guard to ruxolitinib in patients with Grade III or IV Steroid-Refractory acute Graft-Versus-Host Disease (SR-aGVHD). The primary hypothesis is that T-Guard treatment will improve the Day 28 complete response (CR) rate in patients with Grades III and IV SR-aGVHD compared to ruxolitinib.

Full description

Graft-vs-Host Disease (GVHD) is a complication that affects many hematopoietic stem cell transplant (HSCT) patients; it occurs when the new cells from a transplant attack the recipient's body. Acute GVHD (aGVHD) typically develops within the first three months after HSCT and is typically treated with steroid therapy. A significant fraction of the aGVHD population (10-50%) fail to respond to treatment and are deemed steroid-refractory (SR).

Participants that develop Grade III or IV SR aGVHD will be randomized to receive T-Guard or ruxolitinib and will be followed for approximately 180 days. Participants will be stratified by center region (US vs. Europe) and age group (at least 55 years vs. under 55). Participants randomized to the T-Guard arm will receive 4 doses administered intravenously as four 4-hour infusions, and participants randomized to the ruxolitinib arm will receive one dose administered orally twice a day. The primary analysis will include all participants that are randomized.

Enrollment: 12 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

To be eligible to participate in this study, patients must meet the following:

1. Patients must be at least 18.0 years of age at the time of consent.

2. Patient has undergone first allo-HSCT from any donor source or graft source. Recipients of nonmyeloablative, reduced intensity, and myeloablative conditioning regimens are eligible.

3. Patients diagnosed with Grade III/IV SR-aGVHD after allo-HSCT. SR includes aGVHD initially treated at a lower steroid dose, but must meet one of the following criteria:

   • Progressed or new organ involvement after 3 days of treatment with methylprednisolone (or equivalent) of greater than or equal to 2 mg/kg/day
   • No improvement after 7 days of primary treatment with methylprednisolone (or equivalent) of greater than or equal to 2mg/kg/day
   • Patients with visceral (GI and/or liver) plus skin aGVHD at methylprednisolone (or equivalent) initiation with improvement in skin GVHD without any improvement in visceral GVHD after 7 days of primary treatment with methylprednisolone (or equivalent) of greater than or equal to 2mg/kg/day
   • Patients who have skin GVHD alone and develop visceral aGVHD during treatment with methylprednisolone (or equivalent) of greater than or equal to 1mg/kg/day and do not improve after 3 days of greater than or equal to 2mg/kg/day Improvement or progression in organs is determined by comparing current organ staging to staging at initiation of methylprednisolone (or equivalent) treatment.

4. Patients must have evidence of myeloid engraftment (e.g., absolute neutrophil count greater than or equal to 0.5 × 109/L for 3 consecutive days if ablative therapy was previously used). Use of growth factor supplementation is allowed.

5. Patients or an impartial witness (in case the patient is capable of providing verbal consent but not capable of signing the informed consent form (ICF)) should have given written informed consent.

Exclusion criteria

Patients will be excluded from study entry if they meet any of the following exclusion criteria:

1. Patients who have a creatinine greater than or equal to 2mg/dL or estimated creatinine clearance less than 40 mL/min or those requiring hemodialysis.

2. Patients who have been diagnosed with active thrombotic microangiopathy (TMA), defined as meeting all the following criteria:

   • Greater than 4% schistocytes in blood (or equivalent if semiquantitative scale is used e.g., 3+ or 4+ schistocytes on peripheral blood smear)
   • De novo, prolonged or progressive thrombocytopenia (platelet count less than 50 x 109/L or 50% or greater reduction from previous counts)
   • Sudden and persistent increase in lactate dehydrogenase concentration greater than 2x the upper level of normal (ULN)
   • Decrease in hemoglobin concentration or increased transfusion requirement attributed to Coombs-negative hemolysis
   • Decrease in serum haptoglobin

3. Patients who have previously received treatment with eculizumab.

4. Patients who have previously received checkpoint inhibitors (either before or after allo-HCT).

5. Patients who have been diagnosed with overlap syndrome, that is, with any concurrent features of cGVHD.

6. Patients requiring mechanical ventilation or vasopressor support.

7. Patients who have received any systemic treatment, besides steroids, as upfront treatment of aGVHD or as treatment for SR-aGVHD. Reinstitution of previously used GVHD prophylaxis agents (e.g., tacrolimus, cyclosporin, methotrexate [MTX], MMF) or substitutes in cases with previously documented intolerance will be permitted. Previous treatment with a janus kinase (JAK) inhibitor as part of GVHD prophylaxis or treatment is not allowed.

8. Patients who have severe hypoalbuminemia, with an albumin of less than or equal to 1 g/dl.

9. Patients who have a creatine kinase (CK) level of greater than 5 times the upper limit of normal.

10. Patients with uncontrolled infections. Infections are considered controlled if appropriate therapy has been instituted and, at the time of enrollment, no signs of progression are present. Persisting fever without other signs or symptoms will not be interpreted as progressing infection. Progression of infection is defined as:

    • hemodynamic instability attributable to sepsis OR
    • new symptoms attributable to infection OR
    • worsening physical signs attributable to infection OR
    • worsening radiographic findings attributable to infection Patients with radiographic findings attributable to infection within 4 weeks prior to enrollment must have a repeat radiographic exam within one week of enrollment that documents absence of worsening.

11. Patients with evidence of relapsed, progressing, or persistent malignancy, or who have been treated for relapse after transplant, or who may require rapid immune suppression withdrawal as pre-emergent treatment of early malignancy relapse.

12. Patients with evidence of minimal residual disease requiring withdrawal of systemic immune suppression.

13. Patients with unresolved serious toxicity or complications (other than aGVHD) due to previous transplant.

14. History of sinusoidal obstruction syndrome (SOS)/veno-occlusive disease (VOD).

15. Patients with known hypersensitivity to any of the components murine monoclonal antibodies (mAb) or Recombinant Ricin Toxin A-chain (RTA).

16. Patients who have had treatment with any other investigational agent, device, or procedure within 21 days (or 5 half-lives, whichever is greater) prior to enrollment. An investigational agent is defined as medications without any known FDA or European Medicines Agency (EMA) approved indications.

17. Patients who have received more than one allo-HSCT.

18. Patients with known human immunodeficiency virus infection.

19. Patients who have a BMI greater than or equal to 35 kg/m2.

20. Patients who are taking sirolimus must discontinue prior to starting study treatment.

    The sirolimus blood level must be less than 2 ng/mL prior to starting study treatment.

21. Female patients who are pregnant, breast feeding, or, if sexually active and of childbearing potential, unwilling to use effective birth control from start of treatment until 30 days after the last study treatment.

22. Male patients who are, if sexually active and with a female partner of childbearing potential, unwilling to use effective birth control from start of treatment until 65 days after the last study treatment.

23. Patients with any condition that would, in the investigator's judgment, interfere with full participation in the study, including administration of study drug and attending required study visits; pose a significant risk to the patient; or interfere with interpretation of study data.

24. Patients whose decision to participate might be unduly influenced by perceived expectation of gain or harm by participation, such as patients in detention due to official or legal order.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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12 participants in 2 patient groups

T-Guard

Experimental group

Description:

Participants will be administered four doses of T-Guard intravenously for a 4-hour period every other day

Treatment:

Drug: T-Guard

Ruxolitinib

Active Comparator group

Description:

Participants will take ruxolitinib twice daily for continuous daily dosing

Treatment:

Drug: Ruxolitinib