Trial · NCT05848687
TINI 2: Total Therapy for Infants With Acute Lymphoblastic Leukemia II
NCT05848687, Phase 1, Phase 2, Recruiting, Tanja Andrea Gruber
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. TINI 2: Total Therapy for Infants With Acute Lymphoblastic Leukemia II. Trials, record NCT05848687. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05848687
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- TINI 2: Total Therapy for Infants With Acute Lymphoblastic Leukemia II
- NCT number
- NCT05848687
- Status
- Recruiting
- Phases
- Phase 1, Phase 2
- Enrollment
- 90 participants, estimated
- Lead sponsor
- Tanja Andrea Gruber
- Conditions
- Lymphoblastic Leukemia
- Interventions
- Dexamethasone, Mitoxantrone, PEG asparaginase, Bortezomib, Vorinostat, Mercaptopurine, Methotrexate, Blinatumomab, Ziftomenib
- First posted
- 2023-05-08
- Last updated
- 2026-11-12
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Minimal Residual Disease | 5 years and 2 months | Proportion of patients who are minimal residual disease positive at the end of Induction Intensification |
| Secondary | Ziftomenib Minimum safe and Biologically-Effective Dose in Combination with Chemotherapy | 5 years and 6 months | To determine the estimated minimum safe and biologically-effective dose of Ziftomenib in combination with chemotherapy, on the basis of observed DLTs, MRD assessments, and pharmacokinetic studies |
| Secondary | Event Free Survival | 8 years | To estimate the 3-year event-free survival for subjects treated on study |
| Secondary | Overall Survival | 8 years | To estimate the 3-year overall survival for subjects treated on study |
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/NCT05848687
GET https://conductscience.org/api/trials/v1/NCT05848687/registered