Trial · NCT04334993
Pediatric-type Therapy With Pre-transplant Blinatumomab for HR Patients - Phase II Study
NCT04334993, Phase 2, Unknown, Israeli Medical Association
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Pediatric-type Therapy With Pre-transplant Blinatumomab for HR Patients - Phase II Study. Trials, record NCT04334993. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04334993
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Pediatric-type Therapy With Pre-transplant Blinatumomab for HR Patients - Phase II Study
- NCT number
- NCT04334993
- Status
- Unknown
- Phases
- Phase 2
- Enrollment
- 110 participants, estimated
- Lead sponsor
- Israeli Medical Association
- Conditions
- Philadelphia-Negative ALL, High-Risk Cancer
- Interventions
- Blinatumomab
- First posted
- 2020-04-06
- Last updated
- 2021-05-07
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Event-free survival (EFS) | 2 years | Measured from the date of entry on study until treatment failure, relapse from CR, or death from any cause, whichever occurs first |
| Secondary | Overall survival (OS) | 2 years | Measured from the date of entry on study until until death from any cause |
| Secondary | Early death during induction | 60 days | Death during the first 60 days from entering study from any cause |
| Secondary | MRD status | MRD will be assess by PCR after induction I (day 33), after induction II (week 12), after blinatumomab therapy (prior to HSCT) and at days 30 and 100 post alloHSCT. | MRD status pre- and post-antibody-based therapy |
Source ClinicalTrials.gov
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.
Papers1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as |
|---|---|
| 41671463 | DERIVED |
Source PubMed
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.
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/NCT04334993
GET https://conductscience.org/api/trials/v1/NCT04334993/registered