Phase 2 Study in Japanese Patients With Intermediate-2 or High Risk Primary Myelofibrosis, Post-Polycythemia Vera Myelofibrosis, Post-Essential Thrombocythemia Myelofibrosis With Splenomegaly

Myelofibrosis Clinical Trial

Official title:

A Phase 2 Open-Label, Dose-Ranging Study of the Efficacy and Safety of Orally Administered SAR302503 in Japanese Patients With Intermediate-2 or High Risk Primary Myelofibrosis, Post-Polycythemia Vera Myelofibrosis, Post-Essential Thrombocythemia Myelofibrosis With Splenomegaly

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01692366
• Other study ID #: ARD12888
• Secondary ID: U1111-1130-3710
• Status: Completed
• Phase: Phase 2
• First received: September 10, 2012
• Last updated: September 19, 2014
• Start date: November 2012
• Est. completion date: March 2014

Study information

• Verified date: September 2014
• Source: Sanofi
• Contact: n/a
• Is FDA regulated: No
• Health authority: Japan: Ministry of Health, Labor and Welfare
• Study type: Interventional

Clinical Trial Summary

Primary Objective:

• To evaluate the efficacy of daily oral doses of 300 mg, 400 mg, and 500 mg SAR302503 and combined for the response rate defined with the ≥35% reduction of spleen volume as determined by magnetic resonance imaging (MRI or computed tomography scan [CT] in patients with contraindications for MRI).

Secondary Objectives:

• To evaluate the safety of SAR302503 for both pooled (300, 400, and 500mg) and individual doses population.

• To evaluate the pharmacokinetics (PK) of SAR302503 after single and repeat-dose.

• To evaluate the effect on Myelofibrosis (MF)-associated symptoms (Key MF symptoms) as measured by the modified Myelofibrosis Symptom Assessment Form (MFSAF).

• To evaluate the durability of splenic response.

• To evaluate the effect of SAR302503 on bone marrow with regard to changes on reticulin fibrosis.

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 treatment, and an end-of-treatment visit at least 30 days following the last administration of study drug. However, treatment may continue if patients are deriving benefit and do not have unacceptable toxicity or meet study withdrawal criteria.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 8
• Est. completion date: March 2014
• Est. primary completion date: March 2014
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 20 Years and older

Eligibility

Inclusion criteria :

• Diagnosis of primary or post-polycythemia vera or post-essential thrombocythemia myelofibrosis

• Myelofibrosis classified as high-risk or intermediate-risk level 2

• Enlarged spleen, palpable at least 5 cm below costal margin

• Active symptoms of myelofibrosis

• At least 20 years of age

• Eastern Collaborative Oncology Group (ECOG) performance status (PS) of 0, 1, or 2 at study entry

• Absence of active malignancy other than myelofibrosis

• Written informed consent to participate.

Exclusion criteria:

• Splenectomy.

• Any recent 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.

• Major surgery therapy within 28 days or radiation including spleen radiation within 6 months prior to initiation of study drug.

• Concomitant treatment with or use of pharmaceutical or herbal agents known to be moderate or severe inhibitors or inducers CYP3A4.

• 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 JAK 2 Inhibitor.

• Treatment with aspirin in doses >150 mg/day

• Known human immunodeficiency virus or acquired immunodeficiency syndrome-related illness.

• Pregnant or lactating female. Once the lactating female stop and participate in the study, she cannot re-start feeding the baby.

• Women of childbearing potential, unless using effective contraception while on study drug. Otherwise patients must be post-menopausal (at least 1 years from last menstruation without other medical reason), or surgically sterile.

• 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])

The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Myelofibrosis
• Polycythemia
• Polycythemia Vera
• Primary Myelofibrosis
• Splenomegaly
• Thrombocythemia, Essential
• Thrombocytosis

Intervention

Drug:
• SAR302503
Pharmaceutical form:Capsule Route of administration: oral

Locations

Country	Name	City	State
Japan	Investigational Site Number 392010	Akita-Shi
Japan	Investigational Site Number 392002	Bunkyo-Ku
Japan	Investigational Site Number 392006	Bunkyo-Ku
Japan	Investigational Site Number 392004	Sendai-Shi
Japan	Investigational Site Number 392008	Shinjuku-Ku
Japan	Investigational Site Number 392009	Shinjuku-Ku
Japan	Investigational Site Number 392003	Suita-Shi

Sponsors (1)

Lead Sponsor	Collaborator
Sanofi

Country where clinical trial is conducted

Japan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Response Rate (RR), defined as the proportion of subjects who have a =35% reduction as measured by MRI (or CT scan in subjects with contraindications for MRI). - Time Frame:		24 weeks	No
Secondary	Number of patients with Serious Adverse events using NCI CTCAE v4.03, clinical parameters and vital signs		From baseline to the 30 days after last drug administration	Yes
Secondary	Measurements of SAR302503 pharmacokinetic endpoints including Cmax, Tmax, and AUC0-24		SAR302503, pre-dose and post-dose plasma collections will be obtained on Cycle 1 Day 1, Cycle 1 Day 2, Cycle 1 Day 15, Cycle 2 Day 1, Cycle 2 Day 2, and Cycle 3 Day 1	No
Secondary	Symptom Response Rate (SRR): Proportion of subjects with a =50% reduction in the total symptom score using the modified MFSAF		24 weeks	No
Secondary	Duration of maintenance of =35% reduction in spleen volume		From baseline to the 30 days after last drug administration	No
Secondary	Percent change from baseline in spleen volume measured by MRI		24 weeks	No
Secondary	Percent change from baseline in spleen size measured by palpation		24 weeks	No
Secondary	Proportion of patients with any grade reduction in reticulin fibrosis		24 weeks	No