Status:
COMPLETED
Phase 2 Study of SAR302503 in Patients With Myelofibrosis
Lead Sponsor:
Bristol-Myers Squibb
Conditions:
Hematopoietic Neoplasm
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
Primary Objective: \- To evaluate the efficacy of daily oral doses of 300 mg, 400 mg, and 500 mg SAR302503 for the reduction of spleen volume as determined by magnetic resonance imaging (MRI). Secon...
Detailed Description
The duration of the study for an individual patient will include a period to assess eligibility (screening period 28 days), followed by a treatment period of at least 1 cycle (28 days) of study treatm...
Eligibility Criteria
Inclusion
- Inclusion criteria:
- Diagnosis of primary or post-polycythemia vera or post-essential thrombocythemia myelofibrosis (Post-ET MF) according to the 2008 World Health Organization (WHO) criteria
- Myelofibrosis classified as high-risk or intermediate-risk level 2, as defined by International Working Group - Myelofibrosis Research and Treatment (IWG-MRT)
- Enlarged spleen, palpable at least 5 cm below costal margin
- At least 18 years of age.
- Eastern Collaborative Oncology Group (ECOG) performance status (PS) of 0, 1, or 2 at study entry.
- Adequate organ function
- Absence of active malignancy other than MF, except adequately treated basal cell carcinoma and squamous cell carcinoma of the skin, cervical carcinoma in situ or other malignancies that have been stable and off therapy for 5 years.
- Written informed consent to participate.
- Willing to comply with scheduled visits, treatment plans, laboratory assessments, and other study-related procedures.
- Exclusion criteria:
- Splenectomy.
- Any chemotherapy (eg, hydroxyurea), immunomodulatory drug therapy (eg, thalidomide, interferon-alpha), immunosuppressive therapy, corticosteroids \>10 mg/day prednisone or equivalent, or growth factor treatment (eg, erythropoietin), hormones (eg, androgens, danazol) within 14 days prior to initiation of study drug; darbepoetin use within 28 days prior to initiation of study drug.
- Major surgery therapy within 28 days or radiation within 6 months prior to initiation of study drug.
- Concomitant treatment with or use of pharmaceutical or herbal agents known to be at least moderate inhibitors or inducers Cytochrome P450 3A4 (CYP3A4), unless approved by the sponsor.
- Active acute infection requiring antibiotics.
- Uncontrolled congestive heart failure (New York Heart Association Classification 3 or 4), angina, myocardial infarction, cerebrovascular accident, coronary/peripheral artery bypass graft surgery, transient ischemic attack, or pulmonary embolism within 3 months prior to initiation of study drug.
- Participation in any study of an investigational agent (drug, biologic, device) within 30 days, unless during nontreatment phase.
- Prior treatment with a Janus kinase 2 (JAK 2) Inhibitor,
- Contraindications for undergoing Magnetic resonance imaging (MRI) (eg. metal implants).
- Pregnant or lactating female.
- Women of childbearing potential, unless using effective contraception while on study drug.
- Men who partner with a woman of childbearing potential, unless they agree to use effective contraception while on study drug.
- Known human immunodeficiency virus or acquired immunodeficiency syndrome-related illness.
- Clinically active hepatitis B or C.
- Any severe acute or chronic medical, neurological, or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or study drug administration, may interfere with the informed consent process and/or with compliance with the requirements of the study, or may interfere with interpretation of study results and, in the Investigator's opinion, would make the patient inappropriate for entry into this study.
- Unable to swallow capsules
- Presence of any gastric or other disorder that would inhibit absorption of oral medication.
- The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
Exclusion
Key Trial Info
Start Date :
August 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 1 2014
Estimated Enrollment :
30 Patients enrolled
Trial Details
Trial ID
NCT01420770
Start Date
August 1 2011
End Date
April 1 2014
Last Update
March 5 2025
Active Locations (4)
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1
Investigational Site Number 840001
San Francisco, California, United States, 94143
2
Investigational Site Number 840003
Ann Arbor, Michigan, United States, 48109-0759
3
Investigational Site Number 840006
Rochester, Minnesota, United States, 55905
4
Investigational Site Number 840007
Canton, Ohio, United States, 44718