Study Evaluating SKI-606 (Bosutinib) In Japanese Subjects With Philadelphia Chromosome Positive Leukemias

Chronic Myelogenous Leukemia Clinical Trial

Official title:

A Phase 1/2 Study Of Ski-606 Administered As A Single Agent In Japanese Subjects With Philadelphia Chromosome Positive Leukemias

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00811070
• Other study ID #: 3160A4-2203
• Secondary ID: B1871007
• Status: Completed
• Phase: Phase 1/Phase 2
• First received: December 17, 2008
• Last updated: August 7, 2015
• Start date: December 2007
• Est. completion date: June 2015

Study information

• Verified date: August 2015
• Source: Pfizer
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

This is a two-part safety and efficacy study of SKI-606 in subjects who have Philadelphia chromosome positive leukemias (CML). Part 1 will be a dose-escalation study, in which an escalating dose of SKI-606 (Bosutinib), up to 600 mg, will be studied in subjects with imatinib resistant/refractory or imatinib intolerant chronic phase CML. Part 2 will evaluate the safety and efficacy of the maximum tolerated dose (MTD) of SKI-606 (Bosutinib)identified in Part 1 of the study.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 63
• Est. completion date: June 2015
• Est. primary completion date: March 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 20 Years to 74 Years

Eligibility

Inclusion Criteria:

• Cytogenetic or Polymerase Chain Reaction based diagnosis of Chronic phase of Philadelphia Chromosome Positive Chronic Myelogenous Leukemia:

(Part 1), any phase of Philadelphia Chromosome Positive Chronic Myelogenous Leukemia (Part 2), whose disease is resistant/refractory to full-dose imatinib (400 mg for chronic phase subjects/600 mg for advanced leukemia subjects), or are intolerant of any dose of imatinib.

• Adequate duration of prior imatinib therapy.

• No prior exposure to Src, Abl, or Src/Abl kinase inhibitors other than imatinib.

• Eastern Cooperative Oncology Group Performance Status of 0 or 1 for chronic phase subjects, and 0, 1 or 2 for Advanced Stage subjects.

• At least 7 days since any anti-proliferative treatment (including intrathecal chemotherapy) before the first dose of SKI-606, (except hydroxyurea).

• Recovered to National Cancer Institute grade 0-1, or to baseline, from any toxicities of prior anti-tumor treatment, other than alopecia or thrombocytopenia due to active prior treatment (intolerant subjects).

• At least 3 months post allogeneic stem cell transplantation before the first dose of SKI-606.

• Able to take daily oral capsules reliably.

• Absolute neutrophil count greater than 1,000/mL (Part 1)

• Adequate hepatic, and renal function.

• Documented normal INR if not on oral anticoagulant therapy, or, if on oral anticoagulant therapy consistent target INR less than 3.

• Age should be greater than 20 years and less than 75 years (Part 1), greater than 20 years (Part 2), including women of childbearing potential.

• Willingness of male and female subjects, who are not surgically sterile or postmenopausal, must agree and commit to the use of reliable methods of birth control (oral contraceptives, intrauterine devices, or barrier methods used with a spermicide) for the duration of the study and for 30 days after the last dose of SKI-606.

Exclusion Criteria:

• Subjects with Philadelphia chromosome negative Chronic Myelogenous Leukemia.

• Overt leptomeningeal leukemia. Subjects must be free of CNS involvement according to the symptoms for a minimum of 2 months before the first dose of SKI-606. Subjects with CNS symptoms must have a diagnostic lumbar puncture prior to study enrollment.

• Subjects with extramedullary disease only.

• Ongoing requirement for warfarin or other oral anticoagulant therapy (Part 1).

• Ongoing requirement for hydroxyurea (Part 1).

• Graft Versus Host Disease. a. no previous Graft Versus Host Disease allowed (Part 1). b. no treated or untreated Graft Versus Host Disease within 60 days of first dose (Part 2).

• Major surgery within 14 days or radiotherapy within 7 days before the first dose of SKI-606 (recovery from any previous surgery should be complete before day 1).

• Ongoing clinical requirement for administration of a strong inhibitor or inducer of CYP-3A4 (Part 1).

• History of clinically significant or uncontrolled cardiac disease including: a. history of a clinically significant ventricular arrhythmia (such as ventricular tachycardia, ventricular fibrillation, or Torsades de pointes) b. diagnosed or suspected congenital or acquired prolonged QT syndrome c. history of prolonged QTc d. unexplained syncope e. history of or active congestive heart failure f. myocardial infarction within 12 months. g. Uncontrolled angina or hypertension within 3 months.

• Baseline QTcF greater than 0.45 sec (average of triplicate readings).

• Concomitant use of or need for medications known to prolong the QT interval.

• Uncorrected hypomagnesemia or hypokalemia due to potential effects on the QT interval.

• Recent (within 14 days before the first dose of SKI-606) or ongoing clinically significant gastrointestinal disorder.

• Pregnant or breastfeeding women.

• Evidence of serious active infection, or significant medical or psychiatric illness.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Abnormal Karyotype
• Chronic Myelogenous Leukemia
• Leukemia
• Leukemia, Myelogenous, Chronic, BCR-ABL Positive
• Leukemia, Myeloid
• Philadelphia Chromosome

Intervention

Drug:
• SKI-606 (Bosutinib)
Formulation: 100 mg Capsule for Part 1, 100 mg tablet for Part1 and Part 2. SKI-606 (Bosutinib) will be taken by mouth with water and food as continuous once-daily dosing.

Locations

Country	Name	City	State
Japan	Aichi Cancer Center	Aichi
Japan	Japanese Red Cross Nagoya First Hospital	Aichi
Japan	Toyohashi Municipal Hospital	Aichi
Japan	Akita University Hospital	Akita
Japan	Chiba University Hospital	Chiba
Japan	National Cancer Center Hospital	Chuo-ku	Tokyo
Japan	Harasanshin Hospital	Fukuoka
Japan	National Hospital Organization Kyushu Cancer Center	Fukuoka
Japan	Hospital of Hyogo College of Medicine	Hyogo
Japan	Kobe City Medical Center General Hospital	Hyogo
Japan	Kanazawa University Hospital	Ishikawa
Japan	Tokai University Hospital	Kanagawa
Japan	Kumamoto University Hospital	Kumamoto
Japan	University Hospital,Kyoto Prefectural University of Medicine	Kyoto
Japan	Okayama University Hospital	Okayama
Japan	Kinki University School of Medicine	Osaka
Japan	Osaka University Hospital	Osaka
Japan	Saga University Hospital	Saga
Japan	Tohoku University Hospital	Sendai-city	Miyagi
Japan	Hamamatsu Medical Univ. HP Faculty of Medicine	Shizuoka
Japan	Japanese Red Cross Medical Center	Tokyo
Japan	Jikei University Hospital Daisan	Tokyo
Japan	Tokyo Metropolitan Cancer&Infectious disease Ctr Komagome Hp	Tokyo

Sponsors (1)

Lead Sponsor	Collaborator
Pfizer

Country where clinical trial is conducted

Japan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Participants With Dose-Limiting Toxicity (DLT) - Part 1	DLT was defined as any of the following events occurring during the first 28 days of study medication and considered at least possibly-related to study medication: any grade 3 or 4 clinically-relevant non-hematologic toxicity.	Baseline up to Day 28 (Part 1 )	Yes
Primary	Maximum Tolerated Dose (MTD) - Part 1	MTD was defined as highest dose level for which no more than 1 participant in a dose cohort experienced DLT.	Baseline up to Day 28 (Part 1 )	Yes
Primary	Percentage of Participants With Major Cytogenetic Response (MCyR) up to Week 24 in Chronic Phase Second-line Cohort - Part 2	Cytogenetic response (CyR) is based on the prevalence of Philadelphia chromosome positive (Ph+) cells. Major cytogenetic response was categorized as either complete cytogenetic response (CCyR) or partial cytogenetic response (PCyR). CCyR was achieved when there was 0 percent (%) Ph+ cells and PCyR was achieved when 1 to 35% Ph+ cells.	24 weeks	No
Secondary	Maximum Observed Plasma Concentration (Cmax) - Part 1		Before and 1, 2, 3, 4, 6, 8, 24 and 48 hours after administration on Day 1, and before and 1, 2, 3, 4, 6, 8, and 24 hours after administration on Day 15	No
Secondary	Time to Reach Maximum Observed Plasma Concentration (Tmax) - Part 1		Before and 1, 2, 3, 4, 6, 8, 24 and 48 hours after administration on Day 1, and before and 1, 2, 3, 4, 6, 8, and 24 hours after administration on Day 15	No
Secondary	Plasma Decay Half-Life (t1/2) - Part 1	Plasma decay half-life is the time measured for the plasma concentration to decrease by one half.	Before and 1, 2, 3, 4, 6, 8, 24 and 48 hours after administration on Day 1	No
Secondary	Area Under the Concentration-Time Curve (AUC) - Part 1	Area under the plasma concentration time-curve from zero to infinity. AUC on Day 15 was assessed as the steady state AUC.	Before and 1, 2, 3, 4, 6, 8, 24 and 48 hours after administration on Day 1, and before and 1, 2, 3, 4, 6, 8, and 24 hours after administration on Day 15	No
Secondary	Apparent Oral Clearance (CL/F) - Part 1	Clearance of a drug is a measure of the rate at which a drug is metabolized or eliminated by normal biological processes. Clearance obtained after oral dose (apparent oral clearance) is influenced by the fraction of the dose absorbed. Drug clearance is a quantitative measure of the rate at which a drug substance is removed from the blood. CL/F on Day 15 was assessed as the steady state CL/F.	Before and 1, 2, 3, 4, 6, 8, 24 and 48 hours after administration on Day 1, and before and 1, 2, 3, 4, 6, 8, and 24 hours after administration on Day 15	No
Secondary	Apparent Volume of Distribution (Vz/F) - Part 1	Volume of distribution is defined as the theoretical volume in which the total amount of drug would need to be uniformly distributed to produce the desired plasma concentration of a drug. Apparent volume of distribution after oral dose (Vz/F) is influenced by the fraction absorbed.	Before and 1, 2, 3, 4, 6, 8, 24 and 48 hours after administration on Day 1	No
Secondary	Accumulation Ratio (R) - Part 1	R=accumulation ratio (AUCss on Day 15/AUC[0-24] on Day 1)	Before and 1, 2, 3, 4, 6, 8, 24 and 48 hours after administration on Day 1, and before and 1, 2, 3, 4, 6, 8, and 24 hours after administration on Day 15	No
Secondary	Percentage of Participants With Maintained Major Cytogenetic Response (MCyR) at Week 24 in Chronic Phase Second-line and Third-line Cohort - Part 2	"Cytogenetic response (CyR) is based on the prevalence of Philadelphia positive (Ph+) cells. Major cytogenetic response was categorized as either complete cytogenetic response (CCyR) or partial cytogenetic response (PCyR). CCyR was achieved when there was 0 percent (%) Ph+ cells and PCyR was achieved when 1 to 35% Ph+ cells.; The responder for maintained MCyR included 'participants without baseline response who had a response at a specified time' and 'participants with baseline response who had a post-baseline response either maintained or improved at a specified time'."	24 weeks	No
Secondary	Percentage of Participants With Major Cytogenetic Response (MCyR) up to Week 24 - Part 1	Cytogenetic response (CyR) is based on the prevalence of Philadelphia positive (Ph+) cells. Major cytogenetic response was categorized as either complete cytogenetic response (CCyR) or partial cytogenetic response (PCyR). CCyR was achieved when there was 0 percent (%) Ph+ cells and PCyR was achieved when 1 to 35% Ph+ cells.	24 weeks	No
Secondary	Percentage of Participants With Major Cytogenetic Response (MCyR) up to Week 24 in Chronic Phase Third-line Cohort - Part 2	Cytogenetic response (CyR) is based on the prevalence of Philadelphia positive (Ph+) cells. Major cytogenetic response was categorized as either complete cytogenetic response (CCyR) or partial cytogenetic response (PCyR). CCyR was achieved when there was 0 percent (%) Ph+ cells and PCyR was achieved when 1 to 35% Ph+ cells.	24 weeks	No
Secondary	Time to Major Cytogenetic Response (MCyR) in Chronic Phase Second-line and Third-line Cohort - Part 2	"Time to MCyR was the interval from the date of first dose of study medication until the first date of achieving a given response.; Time to response in weeks = (event date minus first dose date plus 1)/7, where the event date is the non-missing date of the first attained response or last cytogenetic assessment date of a participants.	204 weeks in the second-line participants and 48 weeks in the third-line participants	No
Secondary	Duration of Major Cytogenetic Response (MCyR) in Chronic Phase Second-line and Third-line Cohort - Part 2	Duration of MCyR was defined as the interval from the date of the earliest demonstration of a response, until the earliest date of loss of that response.; Duration of response in weeks = (date of confirmed loss of first attained response minus date of first attained response)/7 days.	204 weeks in the second-line participants and 48 weeks in the third-line participants	No
Secondary	Percentage of Participants With Complete Hematologic Response (CHR) up to Week 24 in Advance Phase Second-line Cohort - Part 2	CHR response was considered to be achieved if participants met all of the following criteria: White Blood Cells =< institutional upper limit of normal, no peripheral blood blasts or promyelocytes, myelocytes+metamyelocytes <5% in blood, absolute neutrophil count >=1.0*10^9 per liter (/L), platelets >=100 but <450*10^9/L, <20% basophils in blood and no extramedulary involvement (including hepato- or splenomegaly), =<5% BM blasts.	24 weeks	No
Secondary	Time to Achieve Complete Hematologic Response (CHR) in Advanced Phase Second-line Cohort - Part 2	The time to CHR was measured from the date of first dosing to the first date of response. Time to response in weeks = (event date - first dose date plus 1)/7, where the event date is the non-missing date of the first attained response or last assessment date of a participant.	179 weeks	No
Secondary	Duration of Complete Hematologic Response (CHR) in Advanced Phase Second-line Cohort - Part 2	The duration of CHR was defined as the interval from the first date of response until the first date of confirmed loss of response. Duration of response in weeks =(date of confirmed loss of first attained response - date of first attained response)/7.	179 weeks	No
Secondary	Percentage of Participants With Overall Hematologic Response (OHR) Up to Week 24 in Accelerated Phase/Blast Phase Third-line Cohort - Part 2	OHR included CHR, no evidence of leukemia (NEL), minor hematologic response (MiHR) or return to chronic phase (RCP), participants had to meet at least 1 of this criterion. Criteria for RCP: disappearance of features defining AP/BP, but still in CP and persistence of clonal evolution. Criteria for MiHR: <15% blasts in blood and bone marrow, <30% blasts+promyelocytes in blood and bone marrow, <20% basophils in blood, no extramedullary disease other than liver/spleen. Criteria for CHR and NEL: <20% basophils in blood, no extramedullary involvement including liver/spleen, no peripheral blasts or promyelocytes, myelocytes + metamyelocytes <5% in blood, <5% (NEL) and <=5% (CHR) marrow blasts, 0.5*10^9 <= Absolute neutrophil count (ANC) <1.0*10^9/L (NEL) and ANC>=1.0*10^9/L (CHR), 20*10^9 <=platelets<100 *10^9/L (NEL) and platelets>=100 but <450x10^9/L (CHR), white blood cells <=institutional upper limit of the normal range.	24 weeks	No
Secondary	Time to Achieve Overall Hematologic Response (OHR) in Accelerated Phase/Blast Phase Third-line Cohort - Part 2	The time to OHR was measured from the date of first dosing to the first date of response. Time to response in weeks = (event date - first dose date plus 1)/7, where the event date is the non-missing date of the first attained response or last assessment date of a participant.	48 weeks	No
Secondary	Duration of Overall Hematologic Response (OHR) in Accelerated Phase/Blast Phase Third-line Cohort - Part 2	The duration of OHR was defined as the interval from the first date of response until the first date of confirmed loss of response. Duration of response in weeks =(date of confirmed loss of first attained response - date of first attained response)/7.	48 weeks	No
Secondary	Time to Treatment Failure (TTF) Rate - Part 2	TTF was the interval from the date of first dose of bosutinib until the earlier date of progression or death (any cause), withdrawal from treatment owing to an AE, subject refusal, or loss to follow-up (censored at the last contact date), or further anti-tumor therapy before documented progression (whichever occurred first). TTF rate indicates the probability of no treatment failure. Percent of participants with no treatment failure at Week 48 and Week 96 were estimated.	204 weeks in the second-line participants and 48 weeks in the third-line participants	No
Secondary	Progression-free Survival (PFS) Rate - Part 2	PFS was based on Kaplan-Meier estimates. PFS was defined as time in weeks from start of study treatment to treatment discontinuation due to disease progression as assessed by the investigator. Tumor progression was determined from oncologic assessment data (where data meet the criteria for progressive disease [PD]), or from death case report forms (CRFs). Percent of participants with PFS at Week 48 and Week 96 were estimated.	204 weeks in the second-line participants and 48 weeks in the third-line participants	No
Secondary	Overall Survival (OS) Rate - Part 2	OS was based on Kaplan-Meier method. Survival was defined as the time period from the date of first dose of bosutinib to the date of death, censored at the participant's last contact date. Percent of participants with OS at Week 48 and Week 96 were estimated.	204 weeks in the second-line participants and 48 weeks in the third-line participants	No

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