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An Open Label Study of INCB039110 Administered Orally in Patients With Myelofibrosis

This study is ongoing, but not recruiting participants.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01633372
First Posted: July 4, 2012
Last Update Posted: August 14, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Incyte Corporation
  Purpose
This is a study of itacitinib (INCB039110) in patients with myelofibrosis. This study will evaluate safety and efficacy parameters of itacitinib (INCB039110).

Condition Intervention Phase
Primary Myelofibrosis Post Polycythemia Vera Fibrosis Post Essential Thrombocythemia Myelofibrosis Drug: itacitinib Phase 2

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: An Open-Label, Multiple Simon 2-Stage Study of INCB039110 Administered Orally to Subjects With Primary Myelofibrosis (PMF), Post Polycythemia Vera Myelofibrosis (PPV-MF) or Post Essential Thrombocythemia Myelofibrosis (PET-MF)

Resource links provided by NLM:


Further study details as provided by Incyte Corporation:

Primary Outcome Measures:
  • Proportion of subjects with >/= 50% reduction in total symptom score in each dose group, as measured by the modified The Myelofibrosis Symptom Assessment Form (MFSAF) v3.0 diary [ Time Frame: Baseline and Week 12 ]

Secondary Outcome Measures:
  • Proportion of subjects with >/= 35% reduction in spleen volume, and mean percent change in spleen volume [ Time Frame: Baseline, Week 12 and Week 24 ]
  • Proportion of transfusion dependent subjects who exhibit changes in transfusion frequency over any 12 week period on study and proportion of transfusion independent subjects who exhibit changes in hemoglobin level [ Time Frame: Baseline to Week 12; Week 13 to Week 24 through the end of study or study termination visit. ]
  • Safety and tolerability of itacitinib (INCB039110) as measured by adverse events. [ Time Frame: Every 4-6 weeks through the end of study or early termination visit (approximately 33 weeks exclusive of the extension phase). ]

Estimated Enrollment: 125
Study Start Date: April 2012
Estimated Study Completion Date: January 2018
Primary Completion Date: December 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: itacitinib (INCB039110) 100 mg
itacitinib (INCB039110) 100 mg twice a day
Drug: itacitinib
Other Name: INCB039110
Experimental: itacitinib (INCB039110) 200 mg
itacitinib (INCB039110) 200 mg twice a day
Drug: itacitinib
Other Name: INCB039110
Experimental: itacitinib (INCB039110) 300 mg
itacitinib (INCB039110) 300 mg once a day
Drug: itacitinib
Other Name: INCB039110
Experimental: itacitinib (INCB039110) 400 mg
itacitinib (INCB039110) 400 mg once a day
Drug: itacitinib
Other Name: INCB039110
Experimental: itacitinib (INCB039110) 600 mg
itacitinib (INCB039110) 600 mg once a day
Drug: itacitinib
Other Name: INCB039110

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Must be diagnosed with PMF, PPV-MF or PET-MF as confirmed by bone marrow biopsy.
  • Must score at least 1 point on the Dynamic International Prognostic Scoring System (DIPSS) for prognostic risk factors and have peripheral blast count <10% at both Screening and Baseline hematology assessments.
  • Subjects must discontinue all drugs used to treat underlying MF disease no later than Day -14.
  • Subjects must have hemoglobin value >/= 8.0g/dL and be willing to receive blood transfusions, have a platelet count >/=50x10^9/L and absolute neutrophil count (ANC) >/= 1x10^9/L.
  • Subjects must have palpable spleen or history of splenectomy
  • Active symptoms at the screening visit

Exclusion Criteria:

  • Women who are pregnant or breastfeeding, and men and women who cannot comply with requirements to avoid fathering a child or becoming pregnant, respectively.
  • Subjects with impaired liver function, end stage renal disease on dialysis or clinically significant concurrent infections requiring therapy.
  • Subjects with unstable cardiac function or invasive malignancies over the previous 2 years except treated basal or squamous carcinomas of the skin, completely resected intraepithelial carcinoma of the cervix and completely resected papillary thyroid and follicular thyroid cancers.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01633372


  Show 22 Study Locations
Sponsors and Collaborators
Incyte Corporation
Investigators
Study Director: Albert Assad, MD Incyte Corporation
  More Information

Responsible Party: Incyte Corporation
ClinicalTrials.gov Identifier: NCT01633372     History of Changes
Other Study ID Numbers: INCB 39110-230
First Submitted: June 26, 2012
First Posted: July 4, 2012
Last Update Posted: August 14, 2017
Last Verified: August 2017

Keywords provided by Incyte Corporation:
Primary Myelofibrosis
PMF
Post Polycythemia Vera Fibrosis
PPV-MF
Post Essential Thrombocythemia Myelofibrosis
PET-MF

Additional relevant MeSH terms:
Primary Myelofibrosis
Fibrosis
Polycythemia
Polycythemia Vera
Thrombocytosis
Thrombocythemia, Essential
Pathologic Processes
Myeloproliferative Disorders
Bone Marrow Diseases
Hematologic Diseases
Bone Marrow Neoplasms
Hematologic Neoplasms
Neoplasms by Site
Neoplasms
Blood Platelet Disorders
Blood Coagulation Disorders
Hemorrhagic Disorders