Blinatumomab Consolidation in Real World
Real World Outcomes of Blinatumomab Consolidation in Patients With B-cell Acute Lymphoblastic Leukemia
1 other identifier
observational
200
1 country
1
Brief Summary
This will be a multi-center registry for patients with B-ALL. Patient data will be collected both retrospectively and prospectively. The data forms and surveys will be built and managed through REDCap, a secure web application managed by the Clinical \& Translational Science Institute.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Aug 2025
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 5, 2025
CompletedFirst Posted
Study publicly available on registry
August 12, 2025
CompletedStudy Start
First participant enrolled
August 28, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 14, 2029
ExpectedStudy Completion
Last participant's last visit for all outcomes
May 14, 2029
November 12, 2025
November 1, 2025
3.7 years
August 5, 2025
November 8, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Percentage of participants with complete remission
Complete remission as defined by patients having no lymphoblasts in the marrow or blood
5 years or e.g., 1 year after closure of study
Secondary Outcomes (1)
Overall Survival
5 years
Study Arms (2)
Patients who received Blinatumomab Therapy
Patients who did not receive Blinatumomab Therapy
Eligibility Criteria
Patients with B-ALL diagnosed during or after December 2022
You may qualify if:
- \) aged 18 years or older 2) diagnosed with B-ALL on or after December 1st 2023 3) Not received blinatumomab in an interventional clinical trial setting 4) Willing and able to give informed consent (or retrospective data for deceased patients
You may not qualify if:
- N/A
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Medical College of Wisconsin
Milwaukee, Wisconsin, 53226, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
August 5, 2025
First Posted
August 12, 2025
Study Start
August 28, 2025
Primary Completion (Estimated)
May 14, 2029
Study Completion (Estimated)
May 14, 2029
Last Updated
November 12, 2025
Record last verified: 2025-11
Data Sharing
- IPD Sharing
- Will not share