B-cell Acute Lymphoblastic LeukemiaPhase 2BLASTNCT01207388
Confirmatory Phase II Study of Blinatumomab (MT103) in Patients With Minimal Residual Disease of B-precursor Acute Lymphoblastic Leukemia (ALL)
A Phase 2 study testing Blinatumomab in people with B-cell Acute Lymphoblastic Leukemia, run by Amgen Research (Munich) GmbH at 75 sites in 11 countries.
Trial summary
The purpose of this study is to confirm whether the bispecific T cell engager blinatumomab (MT103) is effective, safe and tolerable in the treatment of ALL patients with minimal residual disease. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- B-cell Acute Lymphoblastic Leukemia
- What is being tested?
- Blinatumomab
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 116 participants
- Where
- 75 sitesin 11 countries
- Study dates
- Nov 2010to 7 Jan 2019
- Phase
- Phase 2
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Patients with B-precursor ALL in complete hematological remission after at least 3 intense chemotherapy blocks
- Presence of minimal residual disease at a level of ≥ 10^-3
- Availability of bone marrow specimen from primary diagnosis for clone-specific MRD assessment
- Negative human immunodeficiency virus (HIV) test, negative hepatitis B (HbsAg) test and hepatitis C virus (anti-HCV) test
- Negative pregnancy test in women of childbearing potential
- Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1
Who cannot join
- Presence of circulating blasts or current extra-medullary involvement by ALL
- History of relevant central nervous system (CNS) pathology or current CNS pathology
- Prior allogeneic hematopoietic stem cell transplant (HSCT)
- Eligibility for treatment with tyrosine-kinase inhibitors (TKI)
- Systemic cancer chemotherapy within 2 weeks prior to study treatment
- Therapy with monoclonal antibodies (rituximab, alemtuzumab) within 4 weeks prior to study treatment
- Previous treatment with blinatumomab
Trial locations and contacts
75 sites in 11 countries.
75 sites in 11 countries
Germany17 sites
1011 - Charité Berlin
Berlin
1022 - Universitätsklinkum Carl Gustav Carus Dresden
Dresden
1009 - Universitätsklinikum Essen
Essen
1002 - Klinikum der Goethe Universität
Frankfurt
1014 - Asklepiosklinik St. Georg
Hamburg
1018 - Medizinische Hochschule Hannover
Hanover
1012 - Universitätsklinikum Heidelberg
Heidelberg
1003 - Universitätsklinikum Schleswig-Holstein
Kiel
1019 - Universitätsklinikum Leipzig
Leipzig
1010 - Klinikum der Universität München - Großhadern
Munich
1004 - Universitätsklinikum Münster
Münster
1016 - Universitätsklinikum Regensburg
Regensburg
1020 - Universitätsklinikum Rostock
Rostock
1007 - Robert-Bosch-Krankenhaus
Stuttgart
1015 - Universitätsklinikum Tübingen
Tübingen
1005 - Universitätsklinikum Ulm
Ulm
1001 - Julius-Maximilians-Universität Würzburg
Würzburg
Italy12 sites
1301 - Ospedali Riuniti di Bergamo
Bergamo
1303 - Istituto di Ematologia "L.& A.Seràgnoli" Azienda
Bologna
1314 - Azienda Ospedaliera Spedali Civili Brescia
Brescia
1313 - Universita di Catania
Catania
1312 - Azienda Ospedaliera Universitaria San Martino
Genoa
1305 - Ospedale San Gerardo
Monza
1309 - Azienda Ospedaliera Antonio Cardarelli
Naples
1308 - Ospedali Riuniti "Villa Sofia-Cervello"
Palermo
1302 - Università La Sapienza di Roma
Rome
1310 - Fondazione Policlinico Tor Vergata
Rome
1315 - Azienda Ospedaliero-Universitaria S. Giovanni Battista (Le Molinette)
Torino
1311 - Azienda Ospedaliera di Verona
Verona
France10 sites
1211 - CHU d'Angers
Angers
1210 - CHU de Besançon
Besançon
1206 - Hôpital de Pontoise
Cergy-Pontoise
1205 - CHU Henri Mondor
Créteil
1209 - CHU de Lyon
Lyon
1212 - Hôpital de l'hôtel Dieu
Nantes
1213 - Centre Hospitalier Universitaire de Nice
Nice
1201 - Hôpital Saint Louis
Paris
1202 - CHU de Bordeaux - Hôpital Haut Lévêque
Pessac
1208 - CHU de Purpan
Toulouse
Poland7 sites
1905 - Uniwersytecki Szpital Kliniczny w Białymstoku
Bialystok
1907 - Uniwersyteckie Centrum Kliniczne
Gdansk
1908 - Swietokrzyskie Centrum Onkologii
Kielce
1902 - Uniwersytet Medyczny w Lublinie
Lublin
1901 - Klinika Hematologii - Instytut Hematologii i Transfuzjologii
Warsaw
1906 - MTZ Clinical Research Sp. z o.o.
Warsaw
1904 - Samodzielny Publiczny
Wroclaw
Spain7 sites
1402 - Complexo Hospitalario Universitario A Coruña
A Coruña
1401 - ICO Hospital Germans Trias I Pujol
Badalona
1404 - Hospital Clínic Servei d´Hematologia
Barcelona
1408 - Hospital 12 de Octubre
Madrid
1405 - Hospital Universitari Son Espases
Mallorca
1407 - Unidad de Citogenética Oncológica
Salamanca
1406 - Hospital Universitari i Politècnic La Fe de Valencia
Valencia
Belgium5 sites
1504
Antwerp
1505
Bruges
1502 - Cliniques Universitaires de Saint-Luc
Brussels
1503
Ghent
1501 - Cliniques Universitaires UCL de Mont Godinne
Yvoir
United Kingdom5 sites
1605 - Queen Elizabeth Hospital
Birmingham
1602 - Bristol Royal Infirmary
Bristol
1604 - University Hospital of Wales
Cardiff
1601 - Royal Free Hospital
London
1607 - Nottingham City Hospital NHS Trust
Nottingham
Austria4 sites
1102 - LKH Graz
Graz
1107 - Krankenhaus der Elisabethinen
Linz
1106
Salzburg
1101 - AKH Wien
Vienna
Romania4 sites
2101 - Institutul Clinic Fundeni, Hematologie II
Bucharest
2102 - Spitalul Clinic Coltea, Hematologie
Bucharest
2106 - Institutul Oncologic "Prof. Dr. I. Chiricuta"
Cluj-Napoca
2105 - Institutul Regional de Oncologie
Iași
Netherlands2 sites
2204 - UMC Groningen
Groningen
2201 - Daniel Den Hoed Hospitaal
Rotterdam
Russia2 sites
2001 - Russian Hematology Research Center
Moscow
2003 - Municipal Hospital No. 15
Saint Petersburg
About this study
Official title: A Confirmatory Multicenter, Single-arm Study to Assess the Efficacy, Safety, and Tolerability of the BiTE® Antibody Blinatumomab in Adult Patients With Minimal Residual Disease (MRD) of B-precursor Acute Lymphoblastic Leukemia (BLAST)
The purpose of this study is to confirm whether the bispecific T cell engager blinatumomab (MT103) is effective, safe and tolerable in the treatment of ALL patients with minimal residual disease.
Read the detailed description
The detection of minimal residual disease (MRD) after induction therapy and/or consolidation therapy is an independent prognostic factor for poor outcome of adult ALL. No standard treatments are available for patients with MRD-positive B-precursor ALL. Blinatumomab (MT103) is a bispecific single-chain antibody construct designed to link B cells and T cells resulting in T-cell activation and a cytotoxic T-cell response against cluster of differentiation (CD)19 expressing cells. The purpose of this study is to confirm whether the bispecific T-cell engager blinatumomab (MT103) is effective, safe and tolerable in the treatment of ALL patients with minimal residual disease.
Participants will receive up to four 4-week cycles of intravenous blinatumomab treatment followed by an infusion-free period of 14 days. A safety follow-up will be performed 30 days after the end of the last infusion and efficacy follow-ups will occur until 24 months after treatment start. Participants will be followed for up to 5 years after the start of treatment for survival.
- Conditions
- B-cell Acute Lymphoblastic Leukemia
- Being tested
- Blinatumomab
- Keywords
- Blinatumomab, MRD, B-ALL, Minimal residual disease, adult ALL, Leukemia, ALL, Lymphatic diseases, Lymphoproliferative disorders, bispecific antibody, anti-CD19, Immunotherapeutic treatment
- Medical subject headings
- Burkitt Lymphoma, Neoplasm, Residual, Precursor Cell Lymphoblastic Leukemia-Lymphoma, Leukemia, Lymphatic Diseases, Lymphoproliferative Disorders
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
BlinatumomabDrug
Also called AMG 103, MT103, BLINCYTO™
Continuous intravenous infusion
| Study group | Role | What they receive |
|---|---|---|
| Blinatumomab | Experimental | Participants received blinatumomab as a continuous intravenous infusion at a constant flow rate of 15 μg/m²/day over 28 days followed by an infusion-free period of 14 days for up to 4 cycles of treatment. Receives: Drug: Blinatumomab |
What is being measured
The primary outcome is the main question the study is designed to answer.
Percentage of Participants With a Minimal Residual Disease (MRD) Response Within the First Treatment Cycle
At the end of the first treatment cycle (Day 29) a bone marrow aspiration/biopsy was performed and evaluated by the central MRD laboratory.
Complete MRD response is defined as no polymerase chain reaction (PCR) amplification of individual rearrangements of immunoglobulin (Ig)- or T-cell receptor (TCR)-genes detected after completion of the first cycle.
Measured: During the first cycle (6 weeks)
Secondary outcomes (11)
Hematological Relapse-free Survival (RFS)
Hematological RFS was measured from first dose of blinatumomab until the first assessment of documented relapse (either hematological or extramedullary), secondary leukemia, or death due to any cause. Participants without a documented relapse, or death due to any cause were censored at the time of their last hematological assessment. Participants who received chemotherapy for relapsed or persistent MRD or for any other reason after treatment with blinatumomab, or HSCT after treatment with blinatumomab, before hematological or extramedullary relapse, or death occurred were censored at the start of chemotherapy or HSCT, respectively.
Hematological relapse was defined as unequivocal detection of > 5% leukemia cells in bone marrow as measured by cytological, microscopic assessment, presence of circulating leukemia blasts, or extramedullary leukemia (whichever occurred first).
The 18-month Kaplan-Meier estimate of hematological RFS is reported.
Measured: 18 months, up to the data cut-off date of 05 August 2015
Overall Survival
Overall survival was measured from the first treatment with blinatumomab until death due to any cause. Participants who did not die were censored at their last contact date.
Measured: Until the data cut-off date of 05 August 2015; median time on study was 18.3 months.
100-Day Mortality After Allogeneic Hematopoietic Stem Cell Transplant
The mortality rate within 100 days after allogeneic HSCT was defined as the Kaplan-Meier estimate of the percentage of participants dying within 100 days after the day of the first allogeneic HSCT.
Measured: 100 days after HSCT, as of the data cut-off date of 05 August 2015
Time to Hematological Relapse
Time to hematological relapse was measured from the start of treatment with blinatumomab until hematological or extramedullary relapse. Participants who died or received HSCT or post-blinatumomab chemotherapy after treatment with blinatumomab were censored at their last hematological assessment prior to death or HSCT or post-blinatumomab chemotherapy (whichever occurred first).
Measured: Until the data cut-off date of 05 August 2015; median time on study was 18.3 months.
Duration of Complete MRD Response
The duration of MRD response was analyzed as the time from onset of MRD negativity until MRD or hematological relapse or date of last confirmation of negative MRD status. Participants who received chemotherapy or HSCT after treatment with blinatumomab, before hematological or extramedullary relapse were censored at the start of chemotherapy or HSCT, respectively.
MRD relapse is defined as the reappearance of individual rearrangements of Ig- or TCR-genes ≥ lower limit of quantification (LLOQ) for at least 1 individual marker measured by an assay with a sensitivity of minimum 10^-4. Hematological relapse is defined as the unequivocal detection of > 5% leukemia cells in bone marrow as measured by cytological or microscopic assessment, presence of circulating leukemia blasts, or extramedullary leukemia.
Measured: Until the data cut-off date of 05 August 2015; median time on study was 18.3 months.
Change in MRD Level From Baseline to End of Cycle 1 in Non-MRD Responders
MRD level was measured by polymerase chain reaction (PCR) performed on bone marrow and assessed by the central laboratory. An MRD level of 10^-n corresponds to residual leukemia cells at a frequency of 1 per 10ⁿ bone marrow cells.
Measured: Baseline and end of cycle 1 (6 weeks)
Number of Participants With Adverse Events
Adverse events (AEs) were evaluated for severity according to the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE), version 4, as follows:
Grade 1 - Mild AE;
Grade 2 - Moderate AE;
Grade 3 - Severe AE;
Grade 4 - Life-threatening or disabling AE;
Grade 5 - Death.
The investigator used medical judgment to determine if there was a causal relationship (ie, related, unrelated) between an adverse event and blinatumomab.
An AE was considered "serious" if it resulted in death, was life-threatening, required or prolonged inpatient hospitalization, resulted in persistent or significant incapacity or substantial disruption to conduct normal life functions, was a congenital anomaly or birth defect or was a medically important condition.
Measured: From the first dose of blinatumomab until 30 days after last dose; the median treatment duration was 55 days.
Change From Baseline in EORTC-QLQ-C30 Scales
The European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire-C30 (EORTC QLQ-C30) is a 30-question tool used to assess the overall quality of life in cancer patients. It consists of 15 domains: 1 global health status (GHS) scale, 5 functional scales (Physical, Role, Cognitive, Emotional, Social), and 9 symptom scales/items (Fatigue, Nausea and Vomiting, Pain, Dyspnea, Insomnia, Appetite Loss, Constipation, Diarrhea, Financial Impact).
For each of these scales, scores range from 0 to 100. For the GHS and 5 functional scales a high score indicates better global health status/functioning and a positive change from baseline indicates improvement. For the 9 symptom scales, a high score indicates a higher level of symptoms, and a negative change from Baseline indicates an improvement in symptoms.
The maximum changes from baseline to cycles 1 through 4 and the change from baseline to the end of the core study are reported.
Measured: Baseline and the end of each treatment cycle (day 29 of each cycle) and 30 days after end of the last infusion (end of the core study, a maximum of 26 weeks).
Change From Baseline in EuroQoL 5-Dimension (EQ-5D) Scales
The EQ-5D is a self-administered questionnaire which captures 3 basic types of information: a descriptive profile (health state index) and the overall health rating using a visual analog scale. The health state index measures mobility, self-care, usual activities, pain/discomfort and anxiety/depression on scales from no problems (score = 1), some problems (score = 2), to extreme problems (score = 3). For each dimension the mean change from baseline was calculated at the end of each treatment cycle and at the end of the core study. The maximum observed change from baseline during cycles 1 to 4 and the change from baseline at the end of the core study are reported for each dimension.
Measured: Baseline and the end of each treatment cycle (day 29 of each cycle) and 30 days after end of the last infusion (end of the core study, a maximum of 26 weeks).
Resource Utilization: Number of Participants Reporting Use of Transfusion of Blood Products
Measured: From first dose of study drug through the end of follow-up; median (minimum, maximum) time on study was 33.8 (1, 62) months
Resource Utilization: Duration of Hospitalization
Measured: From first dose of study drug through the end of follow-up; median (minimum, maximum) time on study was 33.8 (1, 62) months.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 Sep 2010 (estimated)
- Study startNov 2010
- Primary completionFeb 2014
- Study completion7 Jan 2019
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Publications (5)Papers the sponsor has linked to this study.
- Other trials for B-cell Acute Lymphoblastic LeukemiaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 116 participants (actual)
Sponsor and investigators
- Lead sponsor
- Amgen Research (Munich) GmbH
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Ralf Bargou, MD, Principal investigator, Medizinische Klinik und Poliklinik II, WürzburgNicola Gökbuget, MD, Principal investigator, Klinikum der Goethe Universität Frankfurt
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01207388
- Sponsor's protocol ID
- MT103-203
- Acronym
- BLAST
- Status last verified
- Jan 2020
- First submitted
- 21 Sep 2010
- Last updated
- 10 Feb 2020
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
Publications
Chevallier P. Should patients with Ph-negative acute lymphoblastic leukaemia who reach minimal residual disease negativity have HSCT? Lancet Haematol. 2024 Jan;11(1):e12-e13. doi: 10.1016/S2352-3026(23)00365-4. No abstract available.
PubMed 38135369Gokbuget N, Zugmaier G, Dombret H, Stein A, Bonifacio M, Graux C, Faul C, Bruggemann M, Taylor K, Mergen N, Reichle A, Horst HA, Havelange V, Topp MS, Bargou RC. Curative outcomes following blinatumomab in adults with minimal residual disease B-cell precursor acute lymphoblastic leukemia. Leuk Lymphoma. 2020 Nov;61(11):2665-2673. doi: 10.1080/10428194.2020.1780583. Epub 2020 Jul 3.
PubMed 32619115Jen EY, Xu Q, Schetter A, Przepiorka D, Shen YL, Roscoe D, Sridhara R, Deisseroth A, Philip R, Farrell AT, Pazdur R. FDA Approval: Blinatumomab for Patients with B-cell Precursor Acute Lymphoblastic Leukemia in Morphologic Remission with Minimal Residual Disease. Clin Cancer Res. 2019 Jan 15;25(2):473-477. doi: 10.1158/1078-0432.CCR-18-2337. Epub 2018 Sep 25.
PubMed 30254079Gokbuget N, Dombret H, Bonifacio M, Reichle A, Graux C, Faul C, Diedrich H, Topp MS, Bruggemann M, Horst HA, Havelange V, Stieglmaier J, Wessels H, Haddad V, Benjamin JE, Zugmaier G, Nagorsen D, Bargou RC. Blinatumomab for minimal residual disease in adults with B-cell precursor acute lymphoblastic leukemia. Blood. 2018 Apr 5;131(14):1522-1531. doi: 10.1182/blood-2017-08-798322. Epub 2018 Jan 22.
PubMed 29358182Zhu M, Wu B, Brandl C, Johnson J, Wolf A, Chow A, Doshi S. Blinatumomab, a Bispecific T-cell Engager (BiTE((R))) for CD-19 Targeted Cancer Immunotherapy: Clinical Pharmacology and Its Implications. Clin Pharmacokinet. 2016 Oct;55(10):1271-1288. doi: 10.1007/s40262-016-0405-4.
PubMed 27209293
Study at a glance
From the registry record, last updated by the sponsor on 10 Feb 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Confirmatory Multicenter, Single-arm Study to Assess the Efficacy, Safety, and Tolerability of the BiTE® Antibody Blinatumomab in Adult Patients With Minimal Residual Disease (MRD) of B-precursor Acute Lymphoblastic Leukemia (BLAST)
- ClinicalTrials.gov ID
- NCT01207388
- Acronym / sponsor ID
- BLAST / MT103-203
- Conditions
- B-cell Acute Lymphoblastic Leukemia
- Keywords
- Blinatumomab, MRD, B-ALL, Minimal residual disease, adult ALL, Leukemia, ALL, Lymphatic diseases
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 116 participants (actual)
- Lead sponsor
- Amgen Research (Munich) GmbHIndustry (pharma, biotech, devices)
- Study start
- Nov 2010
- Primary completion
- Feb 2014 (actual)
- Study completion
- 7 Jan 2019 (actual)
- First posted
- 22 Sep 2010 (estimated)
- Results
- Posted 12 Feb 2015
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study is to confirm whether the bispecific T cell engager blinatumomab (MT103) is effective, safe and tolerable in the treatment of ALL patients with minimal residual disease.
Detailed description
The detection of minimal residual disease (MRD) after induction therapy and/or consolidation therapy is an independent prognostic factor for poor outcome of adult ALL. No standard treatments are available for patients with MRD-positive B-precursor ALL. Blinatumomab (MT103) is a bispecific single-chain antibody construct designed to link B cells and T cells resulting in T-cell activation and a cytotoxic T-cell response against cluster of differentiation (CD)19 expressing cells. The purpose of this study is to confirm whether the bispecific T-cell engager blinatumomab (MT103) is effective, safe and tolerable in the treatment of ALL patients with minimal residual disease.
Participants will receive up to four 4-week cycles of intravenous blinatumomab treatment followed by an infusion-free period of 14 days. A safety follow-up will be performed 30 days after the end of the last infusion and efficacy follow-ups will occur until 24 months after treatment start. Participants will be followed for up to 5 years after the start of treatment for survival.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Blinatumomab | Experimental | Drug: BlinatumomabParticipants received blinatumomab as a continuous intravenous infusion at a constant flow rate of 15 μg/m²/day over 28 days followed by an infusion-free period of 14 days for up to 4 cycles of treatment. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- Patients with B-precursor ALL in complete hematological remission after at least 3 intense chemotherapy blocks
- Presence of minimal residual disease at a level of ≥ 10^-3
- Availability of bone marrow specimen from primary diagnosis for clone-specific MRD assessment
- Negative human immunodeficiency virus (HIV) test, negative hepatitis B (HbsAg) test and hepatitis C virus (anti-HCV) test
- Negative pregnancy test in women of childbearing potential
Key exclusion criteria (7 listed)
- Presence of circulating blasts or current extra-medullary involvement by ALL
- History of relevant central nervous system (CNS) pathology or current CNS pathology
- Prior allogeneic hematopoietic stem cell transplant (HSCT)
- Eligibility for treatment with tyrosine-kinase inhibitors (TKI)
- Systemic cancer chemotherapy within 2 weeks prior to study treatment
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| BlinatumomabAlso: AMG 103, MT103, BLINCYTO™Continuous intravenous infusion | Drug | Blinatumomab |
Primary outcome
Percentage of Participants With a Minimal Residual Disease (MRD) Response Within the First Treatment Cycle
Time frame: During the first cycle (6 weeks)
At the end of the first treatment cycle (Day 29) a bone marrow aspiration/biopsy was performed and evaluated by the central MRD laboratory. Complete MRD response is defined as no polymerase chain reaction (PCR) amplification of individual rearrangements of immunoglobulin (Ig)- or T-cell receptor (TCR)-genes detected after completion of the first cycle.
11 secondary outcomes
Hematological Relapse-free Survival (RFS)
Time frame: 18 months, up to the data cut-off date of 05 August 2015
Overall Survival
Time frame: Until the data cut-off date of 05 August 2015; median time on study was 18.3 months.
100-Day Mortality After Allogeneic Hematopoietic Stem Cell Transplant
Time frame: 100 days after HSCT, as of the data cut-off date of 05 August 2015
Time to Hematological Relapse
Time frame: Until the data cut-off date of 05 August 2015; median time on study was 18.3 months.
Duration of Complete MRD Response
Time frame: Until the data cut-off date of 05 August 2015; median time on study was 18.3 months.
Change in MRD Level From Baseline to End of Cycle 1 in Non-MRD Responders
Time frame: Baseline and end of cycle 1 (6 weeks)
Number of Participants With Adverse Events
Time frame: From the first dose of blinatumomab until 30 days after last dose; the median treatment duration was 55 days.
Change From Baseline in EORTC-QLQ-C30 Scales
Time frame: Baseline and the end of each treatment cycle (day 29 of each cycle) and 30 days after end of the last infusion (end of the core study, a maximum of 26 weeks).
Change From Baseline in EuroQoL 5-Dimension (EQ-5D) Scales
Time frame: Baseline and the end of each treatment cycle (day 29 of each cycle) and 30 days after end of the last infusion (end of the core study, a maximum of 26 weeks).
Resource Utilization: Number of Participants Reporting Use of Transfusion of Blood Products
Time frame: From first dose of study drug through the end of follow-up; median (minimum, maximum) time on study was 33.8 (1, 62) months
Resource Utilization: Duration of Hospitalization
Time frame: From first dose of study drug through the end of follow-up; median (minimum, maximum) time on study was 33.8 (1, 62) months.
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Feb 2020.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Derived from this study: PubMed 38135369Chevallier P. Should patients with Ph-negative acute lymphoblastic leukaemia who reach minimal residual disease negativity have HSCT? Lancet Haematol. 2024 Jan;11(1):e12-e13. doi: 10.1016/S2352-3026(23)00365-4. No abstract available.
- Derived from this study: PubMed 32619115Gokbuget N, Zugmaier G, Dombret H, Stein A, Bonifacio M, Graux C, Faul C, Bruggemann M, Taylor K, Mergen N, Reichle A, Horst HA, Havelange V, Topp MS, Bargou RC. Curative outcomes following blinatumomab in adults with minimal residual disease B-cell precursor acute lymphoblastic leukemia. Leuk Lymphoma. 2020 Nov;61(11):2665-2673. doi: 10.1080/10428194.2020.1780583. Epub 2020 Jul 3.
- Derived from this study: PubMed 30254079Jen EY, Xu Q, Schetter A, Przepiorka D, Shen YL, Roscoe D, Sridhara R, Deisseroth A, Philip R, Farrell AT, Pazdur R. FDA Approval: Blinatumomab for Patients with B-cell Precursor Acute Lymphoblastic Leukemia in Morphologic Remission with Minimal Residual Disease. Clin Cancer Res. 2019 Jan 15;25(2):473-477. doi: 10.1158/1078-0432.CCR-18-2337. Epub 2018 Sep 25.
- Derived from this study: PubMed 29358182Gokbuget N, Dombret H, Bonifacio M, Reichle A, Graux C, Faul C, Diedrich H, Topp MS, Bruggemann M, Horst HA, Havelange V, Stieglmaier J, Wessels H, Haddad V, Benjamin JE, Zugmaier G, Nagorsen D, Bargou RC. Blinatumomab for minimal residual disease in adults with B-cell precursor acute lymphoblastic leukemia. Blood. 2018 Apr 5;131(14):1522-1531. doi: 10.1182/blood-2017-08-798322. Epub 2018 Jan 22.
- Derived from this study: PubMed 27209293Zhu M, Wu B, Brandl C, Johnson J, Wolf A, Chow A, Doshi S. Blinatumomab, a Bispecific T-cell Engager (BiTE((R))) for CD-19 Targeted Cancer Immunotherapy: Clinical Pharmacology and Its Implications. Clin Pharmacokinet. 2016 Oct;55(10):1271-1288. doi: 10.1007/s40262-016-0405-4.
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B Cell ALL, B-Cell Lymphoma
Active, not recruitingEarly Phase 1
Iomab-ACT: A Pilot Study of 131-I Apamistamab Followed by CD19-Targeted CAR T-Cell Therapy for Patients With Relapsed or Refractory B-Cell Acute Lymphoblastic Leukemia or Diffuse Large B-Cell Lymphoma
B-ALL, DLBCL
RecruitingPhase 1
A Phase I Dose Finding Study of MB-CART2219.1
Lymphoma, CLL
Not yet recruiting
Venetoclax Plus Inotuzumab Reduced-Intensity Induction Sequentially Followed by Blinatumomab in B-ALL
ALL
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Ralf Bargou, MD principal investigator
Medizinische Klinik und Poliklinik II, Würzburg
Nicola Gökbuget, MD principal investigator
Klinikum der Goethe Universität Frankfurt
75 sites in 11 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing Blinatumomab in people with B-cell Acute Lymphoblastic Leukemia, run by Amgen Research (Munich) GmbH at 75 sites in 11 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 10 Feb 2020. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 75 sites in Germany, Italy, France, Poland, Spain and 6 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Yes. Results are posted in the registry (first posted 12 Feb 2015). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Percentage of Participants With a Minimal Residual Disease (MRD) Response Within the First Treatment Cycle (time frame: During the first cycle (6 weeks)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT01207388, which also lists 5 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Feb 2020.