BL-8040 Addition to Consolidation Therapy in AML Patients

Acute Myeloid Leukemia Clinical Trial

— BLAST  

Official title:

A Double- Blind, Placebo Controlled, Randomized, Multicenter, Phase II Study to Assess the Efficacy of BL-8040 Addition to Consolidation Therapy in AML Patients

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02502968
• Other study ID #: UKH062014
• Status: Recruiting
• Phase: Phase 2
• First received: July 6, 2015
• Last updated: September 18, 2015
• Start date: September 2015

Study information

• Verified date: September 2015
• Source: Martin-Luther-Universität Halle-Wittenberg
• Contact: Simone Kowoll, MSc
• Phone: +49-345-5574908
• Email: blast[@]kks-halle.de
• Is FDA regulated: No
• Health authority: Germany: Federal Institute for Drugs and Medical Devices
• Study type: Interventional

Clinical Trial Summary

This study evaluates the addition of BL-8040 to the standard consolidation therapy with cytarabine in the treatment of acute myeloid leukemia (AML) in adults. Half of participants will receive BL-8040 and cytarabine in combination, while the other half will receive placebo and cytarabine.

Description:

The majority of AML patients in first complete Remission (CR) do relapse despite the current consolidation therapy. Leukemic stem cells that are dormant in the bone marrow are presumed to be a major reason for AML relapse. Allogenic stem cell transplantation is an option only for a minority of AML patients in 1st CR. BL-8040 is a novel CXCR4 inhibitor that has a dual mechanism of action: inducing mobilization of leukemic blasts from the bone marrow which enhances cytotoxic effects of chemotherapy and has direct antileukemic, pro-apoptotic properties. The treatment with BL-8040 in combination with consolidation therapy (standard consolidation with high-dose cytarabine) should improve the efficacy of the consolidation therapy resulting in longer lasting remissions.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 194
• Est. primary completion date: July 2018
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Histologically or morphologically confirmed diagnosis of AML except for AML M3 (acute promyelocytic leukemia)

• AML who achieved complete remission (CR), including CRi and CRp after a maximum number of 2 cycles of induction chemotherapy.

• AML subjects younger than 60 years at the time of diagnosis with intermediate or high-risk cytogenetics

• ECOG performance status =2

• Laboratory values as follows (at time of randomization): WBC < 30.000/µl and > 1000/µl, Platelets count > 70.000/µl, Creatinine < 1.0 mg/dl. If creatinine is between 1.0mg/dl and 1.3mg/dl, creatinine clearance should be > 30ml/min as calculated using the Cockroft-Gault formula

• Women of child-bearing potential must practice an acceptable method of birth control until 6 month after the last dose of treatment. Female subjects who are lactating must discontinue nursing prior to the first dose of study drug and should refrain from nursing throughout the treatment period and for 14 days following the last dose of study drug.

• Male with a female partner of childbearing potential using a barrier method of contraception

• Written informed consent

• Subject is able and willing to comply with the requirements of the protocol.

Exclusion Criteria:

• Relapsed or refractory AML

• Start of induction cycle > 90 days before randomization.

• Subjects who have received >2 cycles of induction chemotherapy for AML therapy.

• Subjects younger than 60 years at the time of diagnosis with favorable cytogenetics (t(8;21) or inv(16) or t(16;16) or t(15;17)) or the confirmed presence of the resulting fusion protein AML1-ETO, CBFB-MYH11 or PML-RARA.

• Subjects for which allogeneic HSCT is planned in CR1.

• Planned further maintenance therapy after the end of the protocol defined consolidation therapy.

• Known allergic or hypersensitivity to BL8040- or cytarabine or to any of the test compounds, materials

• Use of investigational device or agents within 2 weeks or less than 5 half lifes for each investigational product /device at the time of enrolment. Registry studies are permissible.

• Abnormal liver function tests: Serum AST/ GOT or ALT/ GPT > 3x upper limit of normal (ULN), Serum bilirubin: Total bilirubin > 2.0mg/dl, conjugated bilirubin > 0.8mg/dl

• O2 saturation < 92% (on room air)

• Concurrent, uncontrolled medical condition, laboratory abnormality, or psychiatric illness which could place the subject at unacceptable risk

• Another malignancy within 3 years of enrolment, except in situ malignancy, or low-risk prostate, skin or cervical cancer after curative therapy. History of other cancer that according to the Investigator might confound the assessment of the endpoints of the study.

• A co-morbid condition which, in the view of the Investigators, renders the subject at high risk from treatment complications.

• History of any or more of the following cardiovascular conditions: cardiac angioplasty (within 6 months) or stenting (within 6 months) and/or myocardial infarction (MI) (within 6 months) or cerebro-vascular event within the past 6 months, unstable angina, vascular disease, class III or IV, congestive heart failure (as defined by the New York Heart Association (NYHA))

• Known central nervous system disease that may jeopardize the subject's study participation according to the investigator judgement

• Active, uncontrolled infection.

• Prior clinically significant grade 3-4 non-hematological toxicity to high-dose cytarabine or grade = 2 of neurological toxicity

• Positive serology for HIV, active Hepatitis C and Hepatitis B (HBsAG pos.) at baseline

• Left ventricular ejection fraction (LVEF) of <40% by multiple gated acquisition (MUGA) scan or echocardiogram (ECHO) at baseline

• Subjects with psychological, psychiatric, neurological, familial, sociological, or geographical conditions that do not permit compliance with the protocol

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Acute Myeloid Leukemia
• Leukemia, Myeloid, Acute

Intervention

Drug:
• Cytarabine

• BL-8040

• Placebo (for BL-8040)
Powder for solution for injection manufactured to mimic BL-8040

Locations

Country	Name	City	State
Germany	Univeritätsklinikum Halle, Klinik Innere Medizin 4	Halle

Sponsors (2)

Lead Sponsor	Collaborator
Dr. Petra Tschanter	BioLineRx, Ltd.

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Relapse Free Survival time	Relapse is defined as recurrence of leukemic blasts (more than 5%) in the bone marrow after confirmed complete remission	18 months	No
Secondary	Overall Survival		18 months	No
Secondary	Time to relapse		18 months	No
Secondary	Relapse free survival		6, 9, 12 and 18 months	No
Secondary	Relapse	Defined as recurrence of leukemic blasts (more than 5%) in the bone marrow after confirmed complete remission	6, 9, 12 and 18 months	No
Secondary	Minimal residual disease	Immunophenotypic characterization of human bone marrow cells will be done to determine MRD	6, 9, 12 and 18 months	No
Secondary	Toxicity	Number and CTC grade of all adverse events related to study treatment analyzed in an descriptive way	enitire study course until 18 months	Yes