Study With SAR302503 in Patients With Polycythemia Vera or Essential Thrombocythemia

Completed · Phase 2

Conditions studied: Hematopoietic Neoplasm

In brief

Primary Objective: * Dose Ranging Phase: To evaluate the efficacy of daily oral doses of 100, 200, and 400 mg SAR302503 in patients with PV and ET who are resistant or intolerant to hydroxyurea (per European LeukemiaNet criteria) for : * Inducing absence of phlebotomy and a hematocrit below 45% for a minimum of 3 months in patients with polycythemia vera, and * Reduction of platelet count to ≤400 x 10x9/L for a minimum of 3 months in patients with essential thrombocythemia. * PV Dose Expansion Phase and ET Dose Ranging Phase (only 600 mg dose group): To evaluate the efficacy of daily oral SAR302503 in patients with PV and ET who are resistant or intolerant to hydroxyurea (per European LeukemiaNet criteria) for: * Inducing absence of phlebotomy eligibility beginning at Day 1 of Cycle 4 visit and continuing through Day 1 of Cycle 6 visit in patients with PV, and * Reduction of platelet count to ≤400 x 10x9/L beginning at Day 1 of Cycle 4 visit and continuing through Day 1 of Cycle 6 visit in patients with ET. Secondary Objectives: * To evaluate the safety of SAR302503. * To evaluate the efficacy of SAR302503 in patients with PV who are resistant or intolerant to hydroxyurea for inducing absence of phlebotomy eligibility. * To evaluate the efficacy of SAR302503 in patients with ET who are resistant or intolerant to hydroxyurea for reduction of platelet counts. * To evaluate the efficacy of SAR302503 in inducing complete and partial responses beginning at Day 1 of Cycle 6 visit through Cycle 8. * To evaluate splenic response as measured by spleen volume using MRI or CT. * To evaluate the pharmacokinetics of SAR302503 after single and repeat doses. * To evaluate the pharmacodynamics of SAR302503 as measured by changes in JAK2V617F allele burden in patients with JAK2V617F mutation, and STAT3 phosphorylation inhibition. * To measure improvement in baseline myeloproliferative neoplasm (MPN)-associated symptoms, as well as overall impact on quality of life. * To measure generic health-related quality of life and utility value using the EuroQol Group (EQ-5DTM) questionnaire.

Key facts

Study ID: NCT01420783
Run by: Bristol-Myers Squibb
People needed: 81
Starts: 2011-10-01
Expected to finish: 2014-05-01
Last updated by the study team: 2025-03-05

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Has had a diagnosis of hydroxyurea resistant or intolerant polycythemia vera (PV) or essential thrombocythemia (ET) documented at Screening.
Polycythemia vera or essential thrombocythemia defined according to the revised WHO criteria.
Polycythemia vera resistance or intolerance to hydroxyurea is defined as polycythemia vera patients on hydroxyurea with a hematocrit >45%, or phlebotomy twice in the last 6 months and at least once in the last 3 months.
Essential thrombocythemia resistance or intolerance to hydroxurea is defined as essential thrombocythemia patients on HU with platelet count >600 x 10x9/L.
Dose Expansion Phase (polycythemia vera) and 600 mg/day group (essential thrombocythemia):
Has had a diagnosis of polycythemia vera or essential thrombocythemia according to the revised WHO 2008 criteria.
PV patients must be resistant or intolerant to hydroxyurea.
ET patients must be resistant or intolerant to hydroxyurea.
Provide written informed consent to participate.

You may not qualify if…

Less than 18 years of age.
Participation in any study of an investigational agent (drug, biologic, device) within 30 days prior to initiation of study drug, unless during non-treatment phase. (Prior treatment with another JAK2 inhibitor is allowed.)
Unwilling to comply with scheduled visits, treatment plans, laboratory assessments, and other study-related procedures.
Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 3 or 4 at study entry.
Splenectomy.
Active malignancy other than polycythemia vera or essential thrombocythemia, 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.
Major surgery within 28 days or radiation within 3 months prior to initiation of study drug.
Active acute infection requiring antibiotics.
Known human immunodeficiency virus or acquired immunodeficiency syndrome-related illness.
Uncontrolled congestive heart failure (New York Heart Association Classification 3 or 4), angina, myocardial infarction, cerebrovascular accident, coronary/peripheral artery bypass surgery, transient ischemic attack, or pulmonary embolism within 3 months prior to initiation of study drug.
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.
Inadequate organ function.
Known active (acute or chronic) Hepatitis A, B, or C; and Hepatitis B and C carriers.
Prior history of chronic liver disease (eg, chronic alcoholic liver disease, autoimmune hepatitis, sclerosing cholangitis, primary biliary cirrhosis, hemachromatosis, non-alcoholic steatohepatitis [NASH]).
Concomitant treatment with or use of drugs or herbal agents known to be at least moderate inhibitors or inducers cytochrome P450 3A4 (CYP3A4).
Presence of any gastric or other disorder that would inhibit absorption of oral medication.
Known hypersensitivity to any excipients in the study drug formulation.
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.
The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Where it is running

Investigational Site Number 840008 — Scottsdale, Arizona, United States
Investigational Site Number 840004 — La Jolla, California, United States
Investigational Site Number 840005 — Los Angeles, California, United States
Investigational Site Number 840011 — Palo Alto, California, United States
Investigational Site Number 840010 — Ann Arbor, Michigan, United States
Investigational Site Number 840007 — Rochester, Minnesota, United States
Investigational Site Number 840003 — St Louis, Missouri, United States
Investigational Site Number 840001 — Houston, Texas, United States
Investigational Site Number 036001 — Clayton, Australia
Investigational Site Number 036002 — Kingswood, Australia
Investigational Site Number 036004 — Kogarah, Australia
Investigational Site Number 036003 — Randwick, Australia
Investigational Site Number 124002 — Montreal, Canada
Investigational Site Number 124003 — Toronto, Canada
Investigational Site Number 124001 — Vancouver, Canada
Investigational Site Number 250004 — Brest, France
Investigational Site Number 250003 — Marseille, France
Investigational Site Number 250001 — Paris, France
Investigational Site Number 276004 — Frankfurt am Main, Germany
Investigational Site Number 276003 — Mannheim, Germany
Investigational Site Number 380003 — Bologna, Italy
Investigational Site Number 380001 — Florence, Italy
Investigational Site Number 380004 — Orbassano, Italy
Investigational Site Number 410001 — Seongnam, South Korea
Investigational Site Number 410003 — Seoul, South Korea

Full record on ClinicalTrials.gov

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