Inotuzumab B1931036 (ALL)
Recruiting
Who can enter
Children with confirmed diagnosis of high-risk first relapse of acute lymphoblastic leukemia (ALL)
Age: 1 to <18 years
Goal
Goal
There is an urgent need to improve the efficacy (removal of cancer cells) of reinduction therapy and reduce treatment side effects. Therefore, the purpose of this study is to evaluate whether inotuzumab ozogamicin is more effective in removing cancer cells after one treatment cycle than ALLR3, the standard multi-agent chemotherapy regimen.
Background
Background
Children with ALL are currently treated with different treatment protocols. All children start with what is known as induction treatment. Treatment with ALLR3 chemotherapy is considered the standard first-line treatment for ALL by many physicians and study groups.
However, in high-risk patients ALLR3 has not been as effective in removing cancer cells with fewer side effects as it has been in other risk groups. Modern treatment approaches for ALL focus on pre-transplant removal of cancer cells, especially for patients with high-risk disease characteristics. Inotuzumab ozogamicin is expected to improve response to treatment, with fewer side effects after one treatment cycle.
Bone marrow, blood and cerebrospinal fluid samples will be collected several times during treatment to determine response rates.
The study is being conducted in 60 or more research sites in about 19 countries, mainly in Europe. In the Netherlands, the study is conducted at the Prinses Máxima Center.
In order to participate in a study please refer to your/your child’s doctor.
For international patients: please feel welcome to contact our International Patients Office.
Last reviewed
Last reviewed
March 23, 2026
Study details
- Study details
Official title
A prospective, randomized, open-label phase 2 study to evaluate the superiority of inotuzumab ozogamicin monotherapy versus ALLR3 for induction treatment of childhood high risk first relapse B-cell precursor acute lymphoblastic leukemiaCancer type
First relapse of B-cell precursor acute lymphoblastic leukemiaPhase
2Maximum number of patients
100 worldwide, of whom 2-4 are expected to participate in the NetherlandsStart date
September 5, 2023Status
OpenLocal principal investigator
Dr. B.J. VormoorSponsor
Pfizer Inc.Approval
The study of this new treatment has been reviewed by an accredited medical research ethics committee. This committee has decided that it is justified to ask patients to participate in this study. More information can be found at: CCMO.Trial registry number
EU Clinical Trials Register: 2022-000186-40
The above information is intended as a brief summary only and may not reflect the most up-to-date information. For full details and the current status of a protocol, physicians can contact the Princess Máxima Center directly.