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Phase 2 N=21 Treatment

Phase II Study of the BiTE® Blinatumomab (MT103) in Patients With Minimal Residual Disease of B-precursor Acute Lymphoblastic Leukemia (ALL)

Acute Lymphoblastic Leukemia

Enrolled (actual)
21
Serious AEs
47.6%
Results posted
Jan 2015
Primary outcome: Primary: Percentage of Participants With a Minimal Residual Disease (MRD) Response Within 4 Cycles of Treatment — 80.0 percentage of participants — p=0.0000

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Blinatumomab (MT103) (Biological)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Amgen Research (Munich) GmbH
Primary completion
Sep 2009

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Participants With a Minimal Residual Disease (MRD) Response Within 4 Cycles of Treatment
80.0 0.0000 sig
SECONDARY
Percentage of Participants With an MRD Response After Each Treatment Cycle
80.0; 80.0; 80.0; 80.0
SECONDARY
Time to Hematological Relapse
NA
SECONDARY
Time to MRD Progression
221.0
SECONDARY
Time to MRD Relapse
NA
SECONDARY
Number of Participants With Adverse Events
21; 17; 21; 13; 10; 9
SECONDARY
Change From Screening Value in B-cell Count During Cycle 1
0.0181; -0.0098; -0.0361; -0.0435; -0.0417; -0.0403
SECONDARY
Change From Screening Value in T-cell Count During Cycle 1
-0.0418; -0.3208; -0.4976; -0.5227; -0.5390; -0.4780
SECONDARY
Serum Cytokine Peak Levels in Cycle 1
NA; NA; 693.2; NA; 1135.3; 408.5
SECONDARY
Serum Blinatumomab Concentration at Steady State
696
SECONDARY
Area Under the Drug Concentration-time Curve From Time Zero to Infinity
481
SECONDARY
Apparent Volume of Distribution
2.00
SECONDARY
Clearance of Blinatumomab
0.939
SECONDARY
Terminal Half-life of Blinatumomab
1.47

Summary

The purpose of this study is to determine whether the bispecific T-cell engager (BiTE®) Blinatumomab (MT103) is effective in the treatment of ALL patients with minimal residual disease.

Eligibility Criteria

Inclusion Criteria

  • B-precursor ALL patients in complete hematological remission with molecular failure or molecular relapse starting at any time after consolidation I of front-line therapy within German Multicenter Study Group on Adult Acute Lymphoblastic Leukemia (GMALL) standards or at any time outside GMALL standards.
  • Patients must have a molecular marker for evaluation of minimal residual disease which is either Breakpoint cluster region/gene on human chromosome #9 (Bcr/abl) at any detection level or individual rearrangements of immunoglobulin or T-cell receptor (TCR)-genes measured by an assay with a sensitivity of minimum 10^-4: At least one individual marker at a quantitative level ≥ 10^-4.
  • Eastern Cooperative Oncology Group (ECOG) Performance Status < 2
  • Ability to understand and willingness to sign a written informed consent
  • Signed and dated written informed consent is available

Exclusion Criteria

  • Current extra medullar involvement
  • History of or current relevant central nervous system (CNS) pathology (except migraine/headache and/or previous infiltration of cerebrospinal fluid (CSF) by ALL)
  • Current infiltration of cerebrospinal fluid by ALL
  • History of or current autoimmune disease
  • Autologous stem cell transplantation within 6 weeks prior to study entry
  • Any prior allogeneic stem cell transplantation
  • Cancer chemotherapy within 4 weeks prior to study treatment (except for intrathecal prophylaxis and/or low dose maintenance therapy such as vinca alkaloids, mercaptopurine, methotrexate, steroids)
  • Radiotherapy within 4 weeks prior to study treatment
  • Therapy with monoclonal antibodies (Rituximab, MabCampath) within 6 weeks prior to study treatment
  • Known hypersensitivity to immunoglobulins or to any other component of the study drug formulation
  • Presence of human anti-murine antibodies (HAMA)
  • Abnormal bone marrow, renal or hepatic function
  • Indication for a hypercoagulative state
  • History of malignancy other than ALL within 5 years prior to study entry, with the exception of basal cell carcinoma of the skin or cervix carcinoma in situ
  • Active severe infection, any other concurrent disease or medical condition that are deemed to interfere with the conduct of the study as judged by the investigator
  • Known infection with human immunodeficiency virus (HIV) or chronic infection with hepatitis B virus (HbsAg positive) or hepatitis C virus (anti-HCV positive)
  • Pregnant or nursing women
  • Women of childbearing potential not willing to use an effective form of contraception during participation in the study and at least 3 months thereafter or male patients not willing to ensure effective contraception during participation in the study and at least three months thereafter
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00560794). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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