Study Stopped
the study was closed early due to competing trials
Combination Chemotherapy and Inotuzumab Ozogamicin in Treating Patients With B Acute Lymphoblastic Leukemia
Phase II Study of the Hyper-CVAD Regimen in Sequential Combination With Inotuzumab Ozogamicin as Frontline Therapy for Adults With B-Cell Lineage Acute Lymphocytic Leukemia
3 other identifiers
interventional
4
1 country
1
Brief Summary
This phase II trial studies how well combination chemotherapy and inotuzumab ozogamicin work in treating patients with B acute lymphoblastic leukemia. Drugs used in chemotherapy, such as cyclophosphamide, vincristine sulfate, doxorubicin hydrochloride, dexamethasone, methotrexate and cytarabine, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Immunotherapy with monoclonal antibodies, such as inotuzumab ozogamicin, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Giving combination chemotherapy and inotuzumab ozogamicin may work better at treating B acute lymphoblastic leukemia.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for phase_2
Started Mar 2018
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
Study Start
First participant enrolled
March 28, 2018
CompletedFirst Submitted
Initial submission to the registry
March 29, 2018
CompletedFirst Posted
Study publicly available on registry
April 4, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 2, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
April 2, 2020
CompletedResults Posted
Study results publicly available
April 13, 2021
CompletedJuly 16, 2024
July 1, 2024
2 years
March 29, 2018
January 28, 2021
July 3, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
Event-Free Survival
Event-free survival defined as the time interval from date of treatment start until the date of death, disease progression or relapse.
Start of treatment up to 2 years
Secondary Outcomes (4)
Overall Survival
Start of treatment up to 2 years
Participants to Achieve Complete Remission (CR):
Start of treatment up to 2 years
Number of Participants With Minimal Residual Disease (MRD) Negativity
Start of treatment up to 2 years
Number of Participants With Adverse Events
Start of treatment up to 30 days after last dose received.
Study Arms (1)
Treatment (hyper-CVAD, inotuzumab ozogamicin)
EXPERIMENTALSee detailed description.
Interventions
Given IV
Given IT or IV
Given IV or PO
Given IV
Given IV
Given IV
Given PO
Given IT, IV or PO
Given IV
Given PO
Given IV
Given IV
Eligibility Criteria
You may qualify if:
- Patients with newly diagnosed, previously untreated B-lineage ALL, or having achieved complete remission (CR) with one course of induction chemotherapy
- Patients with extramedullary disease only are eligible
- Failure to one induction course of chemotherapy (these patients will be analyzed separately)
- Performance status of 0-3
- Creatinine less than or equal to 2.0 mg/dL (unless considered tumor related)
- Bilirubin less than or equal to 2.0 mg/dL (unless considered tumor related)
- Adequate cardiac function as assessed by history and physical examination
- No active or co-existing malignancy with life expectancy less than 12 months
- Women of childbearing potential (WOCBP) or male subjects with a partner who is WOCBP must agree to use contraception during the study, if sexually active
You may not qualify if:
- Pregnant or nursing women
- Known to be human immunodeficiency virus (HIV)-positive
- Philadelphia chromosome (Ph)-positive ALL
- Active and uncontrolled disease/infection as judged by the treating physician
- Unable or unwilling to sign the consent form
- Subjects who have current active hepatic or biliary disease (with exception of patients with Gilbert's syndrome, asymptomatic gallstones, liver involvement or stable chronic liver disease per investigator assessment)
- Chronic or current infectious disease requiring systemic antibiotics, antifungal, or antiviral treatment such as, but not limited to, chronic renal infection, chronic chest infection with bronchiectasis, tuberculosis and active hepatitis C
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- M.D. Anderson Cancer Centerlead
- National Cancer Institute (NCI)collaborator
Study Sites (1)
M D Anderson Cancer Center
Houston, Texas, 77030, United States
Related Links
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Results Point of Contact
- Title
- Elias Joseph Jabbour, MD./ Professor
- Organization
- The University of Texas MD Anderson Cancer Center
Study Officials
- PRINCIPAL INVESTIGATOR
Elias Jabbour
M.D. Anderson Cancer Center
Publication Agreements
- PI is Sponsor Employee
- Yes
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 29, 2018
First Posted
April 4, 2018
Study Start
March 28, 2018
Primary Completion
April 2, 2020
Study Completion
April 2, 2020
Last Updated
July 16, 2024
Results First Posted
April 13, 2021
Record last verified: 2024-07