Study of Itacitinib in Combination With Corticosteroids for the Treatment of Acute GVHD

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Incyte

Status and phase

Completed
Phase 1

Conditions

Graft-versus-host Disease (GVHD)

Treatments

Drug: Itacitinib (200 mg)
Drug: Itacitinib (300 mg)
Drug: prednisone or methylprednisolone (corticosteroids)

Study type

Interventional

Funder types

Industry

Identifiers

NCT02614612
INCB 39110-108

Details and patient eligibility

About

To determine if Itacitinib in combination with corticosteroids is safe and tolerable in patients with Grade IIB-IVD acute graft-versus-host disease (GVHD).

Enrollment

31 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Have undergone first allo-HSCT from any donor source (matched unrelated donor, sibling, haploidentical) using bone marrow, peripheral blood stem cells, or cord blood for hematologic malignancies. Recipients of nonmyeloablative and myeloablative transplants are eligible.
  • Clinically suspected Grades IIB to IVD acute GVHD as per modified MN-CIBMTR criteria, occurring after allo-HSCT with any conditioning regimen and any anti-GVHD prophylactic program.

Subjects may, but are not required to, have previously received corticosteroids for acute GVHD:

  • Evidence of myeloid engraftment. Use of growth factor supplementation is allowed.

Exclusion criteria

  • Has received more than 1 hematopoietic stem cell transplantation.
  • Has progressed on more than 2 prior treatment regimens for acute GVHD.
  • Presence of an active uncontrolled infection.
  • Subjects with relapsed primary disease, or subjects who have been treated for relapse after the allogeneic hematopoietic stem-cell transplantation (allo-HSCT) was performed.
  • Inadequate recovery from toxicity and/or complications from the prior allo-HSCT.
  • Any corticosteroid therapy (for indications other than GVHD) at doses > 1 mg/kg per day methylprednisolone or equivalent within 7 days of randomization.
  • Previously received JAK inhibitor therapy for any indication.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

31 participants in 2 patient groups

Itacitinib (200 mg)
Experimental group
Description:
Itacitinib (200 mg) + prednisone or methylprednisolone (corticosteroids)
Treatment:
Drug: prednisone or methylprednisolone (corticosteroids)
Drug: Itacitinib (200 mg)
Itacitinib (300 mg)
Experimental group
Description:
Itacitinib (300 mg) + prednisone or methylprednisolone (corticosteroids)
Treatment:
Drug: prednisone or methylprednisolone (corticosteroids)
Drug: Itacitinib (300 mg)

Trial contacts and locations

23

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Data sourced from clinicaltrials.gov

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