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Trial · NCT03913559

Inotuzumab Ozogamicin for Children With MRD Positive CD22+ Lymphoblastic Leukemia

NCT03913559, Phase 2, Terminated, St. Jude Children's Research Hospital

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Inotuzumab Ozogamicin for Children With MRD Positive CD22+ Lymphoblastic Leukemia. Trials, record NCT03913559. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03913559

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Inotuzumab Ozogamicin for Children With MRD Positive CD22+ Lymphoblastic Leukemia
NCT number
NCT03913559
Status
Terminated
Phases
Phase 2
Enrollment
5 participants, actual
Lead sponsor
St. Jude Children's Research Hospital
Conditions
Acute Lymphoblastic Leukemia
Interventions
Inotuzumab ozogamicin, Methotrexate, Hydrocortisone, Cytarabine, Diphenhydramine, Acetaminophen, Methylprednisolone
First posted
2019-04-12
Last updated
2026-02-12

Source ClinicalTrials.gov

Registered outcomes8

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryTreatment response Cycle1 - countAt the end of cycle 1 (each cycle is 28 days)Number of patients that reach MRD negative at the end of cycle 1
PrimaryTreatment Response Cycle 1 - percentageAt the end of cycle 1 (each cycle is 28 days)Percentage of patients that reach MRD negative at the end of cycle 1
PrimaryTreatment Response Cycle 2 - countAt the end of cycle 2 (each cycle is 28 days)Number of patients that reach MRD negative at the end of cycle 2
PrimaryTreatment Response Cycle 2 - percentageAt the end of cycle 2 (each cycle is 28 days)Percentage of patients that reach MRD negative at the end of cycle 2
SecondaryOccurrence of death - countup to 30 days from last dose of inotuzumab ozogamicin or up to 30 days post-transplant among the patients who proceed to transplantNumber of patient deaths that occur at any time during observation on study
SecondaryOccurrence of death - percentageup to 30 days from last dose of inotuzumab ozogamicin or up to 30 days post-transplant among the patients who proceed to transplantPercentage of patient deaths that occur at any time during observation on study
SecondaryOccurrence of Veno-occlusive disease (VOD) - countup to 30 days from last dose of inotuzumab ozogamicin or up to 30 days post-transplant among the patients who proceed to transplantNumber of patients that develop VOD at any time during observation on study
SecondaryOccurrence of Veno-occlusive disease (VOD) - percentageup to 30 days from last dose of inotuzumab ozogamicin or up to 30 days post-transplant among the patients who proceed to transplantPercentage of patients that develop VOD at any time during observation on study

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers2

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
35622074DERIVEDPubMed
41671463DERIVEDPubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT03913559

GET https://conductscience.org/api/trials/v1/NCT03913559/registered