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Phase 3 Completed N=439 Randomized Double-blind Treatment

GRAVITAS-301: A Study of Itacitinib or Placebo in Combination With Corticosteroids for Treatment of Acute Graft-Versus-Host Disease

Graft-versus-host Disease (GVHD)
Source: ClinicalTrials.gov NCT03139604 ↗
Enrolled (actual)
439
Serious AEs
61.3%
Results posted
May 2020
Primary outcomePrimary: Overall Response Rate Based on Center for International Blood and Marrow Transplant Research (CIBMTR) Response Index — 74.0; 66.4 Percentage of Participants — p=0.0782
◆ Published Evidence
Established
63citations · ~16 / year
Efficacy and safety of itacitinib versus placebo in combination with corticosteroids for initial treatment of acute graft-versus-host disease (GRAVITAS-301): a randomised, multicentre, double-blind, phase 3 trial.
The Lancet. Haematology · 2022 · Likely link

Summary

The purpose of this study is to evaluate itacitinib or placebo in combination with corticosteroids as first-line treatment of participants with Grade II to IV acute graft-versus-host disease (aGVHD).

Linked Publications (2)

  • Efficacy and safety of itacitinib versus placebo in combination with corticosteroids for initial treatment of acute graft-versus-host disease (GRAVITAS-301): a randomised, multicentre, double-blind, phase 3 trial.
    The Lancet. Haematology · 2022 · 63 citations · Likely link
  • A biomarker signature to predict complete response to itacitinib and corticosteroids in acute graft-versus-host disease.
    British journal of haematology · 2022 · 10 citations · Open access · Likely link

Outcome Measures

OutcomeResultp-value
PRIMARY
Overall Response Rate Based on Center for International Blood and Marrow Transplant Research (CIBMTR) Response Index
74.0; 66.4 0.0782
SECONDARY
Nonrelapse Mortality
36; 37; 46; 45; 51; 52 —
SECONDARY
Duration of Response
587; NA —
SECONDARY
Cmax of Itacitinib When Administered in Combination With Corticosteroids
796 —
SECONDARY
Cmin of Itacitinib When Administered in Combination With Corticosteroids
72.5 —
SECONDARY
Tmax of Itacitinib When Administered in Combination With Corticosteroids
2.1 —
SECONDARY
AUC of Itacitinib When Administered in Combination With Corticosteroids
6720 —
SECONDARY
CL/F of Itacitinib When Administered in Combination With Corticosteroids
104 —
SECONDARY
Time to Response
9.9; 10.1 —
SECONDARY
Relapse Rate of Malignant and Nonmalignant Hematologic Disease
12.4; 11.4 —
SECONDARY
Malignancy Relapse-related Mortality Rate
6.4; 7.7 —
SECONDARY
Failure-free Survival
44.29; 40.00 —
SECONDARY
Overall Survival (OS)
365; 348.5 —
SECONDARY
Number of Treatment-emergent Adverse Events With INCB39110
208; 214 —
SECONDARY
Incidence Rate of Secondary Graft Failure
2; 0 —
SECONDARY
Proportion of Subjects Who Discontinue Corticosteroids
3; 3; 16; 11; 39; 45 —
SECONDARY
Proportion of Subjects Who Discontinue Immunosuppressive Medications
12; 10; 11; 8 —
SECONDARY
Incidence Rate of aGVHD Flares
42; 48 —
SECONDARY
Incidence Rate of cGVHD
25; 36; 43; 58 —
SECONDARY
Objective Response Rate
170; 160; 138; 124; 92; 96 —

Eligibility Criteria

Inclusion Criteria

  • Has undergone 1 allo-HSCT from any donor (related or unrelated with any degree of HLA matching) and any donor source (bone marrow, peripheral blood stem cells, or cord blood) for a hematologic malignancy or disorder. Recipients of myeloablative and reduced-intensity conditioning regimens are eligible.
  • Clinically suspected Grade II to IV aGVHD as per MAGIC criteria, occurring after allo-HSCT and any GVHD prophylaxis regimen.
  • Evidence of myeloid engraftment. Use of growth factor supplementation is allowed.
  • Serum creatinine ≤ 2.0 mg/dL or creatinine clearance ≥ 40 mL/min measured or calculated by Cockroft Gault equation.
  • Willing to avoid pregnancy or fathering children.
  • Able to give written informed consent and comply with all study visits and procedures.
  • Able to swallow and retain oral medication.

Exclusion Criteria

  • Has received more than 1 allo-HSCT.
  • Has received more than 2 days of systemic corticosteroids for aGVHD.
  • Presence of GVHD overlap syndrome.
  • Presence of an active uncontrolled infection.
  • Known human immunodeficiency virus infection.
  • Active hepatitis B virus (HBV) or hepatitis C virus infection that requires treatment or at risk for HBV reactivation.
  • Participants with evidence of relapsed primary disease, or participants who have been treated for relapse after the allo-HSCT was performed.
  • Any corticosteroid therapy for indications other than GVHD at doses > 1 mg/kg per day methylprednisolone (or prednisone equivalent) within 7 days of randomization.
  • Severe organ dysfunction unrelated to underlying GVHD, including:
  • Cholestatic disorders or unresolved veno-occlusive disease of the liver.
  • Clinically significant or uncontrolled cardiac disease.
  • Clinically significant respiratory disease that requires mechanical ventilation support or 50% oxygen.
  • Currently breast feeding.
  • Received JAK inhibitor therapy after allo-HSCT for any indication. Treatment with a JAK inhibitor before allo-HSCT is permitted.
  • Treatment with any other investigational agent, device, or procedure within 21 days (or 5 half-lives, whichever is greater) of enrollment.
  • Any medical complications or conditions 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 participant; or interfere with interpretation of study data.
  • Known allergies, hypersensitivity, or intolerance to any of the study medications, excipients, or similar compounds.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03139604) and the linked publication. Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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