Trial · NCT02881086
Optimization of Therapy in Adult Patients With Newly Diagnosed Acute Lymphoblastic Leukemia or Lymphoblastic Lymphoma by Individualised, Targeted and Intensified Treatment
NCT02881086, Phase 3, Completed, Goethe University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Optimization of Therapy in Adult Patients With Newly Diagnosed Acute Lymphoblastic Leukemia or Lymphoblastic Lymphoma by Individualised, Targeted and Intensified Treatment. Trials, record NCT02881086. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02881086
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Optimization of Therapy in Adult Patients With Newly Diagnosed Acute Lymphoblastic Leukemia or Lymphoblastic Lymphoma by Individualised, Targeted and Intensified Treatment
- NCT number
- NCT02881086
- Status
- Completed
- Phases
- Phase 3
- Enrollment
- 1,023 participants, actual
- Lead sponsor
- Goethe University
- Conditions
- Acute Lymphoblastic Leukemia, Lymphoblastic Lymphoma
- Interventions
Rituximab, Nelarabine, PEG-Asparaginase, Cranial irradiation, Imatinib, Idarubicin, Dexamethasone, Cyclophosphamide, Fludarabine, Vincristine, Mercaptopurine, VP16, Daunorubicin (DNR), Methotrexate, Stem cell transplantation, Cytarabine, Vindesine, Adriamycin, Prednisolone
- First posted
- 2016-08-26
- Last updated
- 2025-12-16
Source ClinicalTrials.gov
Registered outcomes17
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Event free survival | 3.5 years | |
| Secondary | Time until consolidation treatment I | approximately 70 days | |
| Secondary | Disease free survival | 1 year | |
| Other | Hematological remission rate | after induction, approximately 6-8 weeks from diagnosis | |
| Other | Molecular remission rate | after induction and consolidation, approximately 6-8 weeks from diagnosis | |
| Other | Results of the positron emission tomography (PET) based remission evaluation | after consolidation, approximately 8-10 weeks | |
| Other | Remission duration | up to 10 years | |
| Other | Relapse rate | up to 10 years | |
| Other | Overall survival | up to 10 years | |
| Other | Relapse location | at timepoint of relapse (up to 10 years) |
1 to 10 of 17Source ClinicalTrials.gov
See all 17 registered outcomesOutcomes0
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 |
|---|---|
| 42477805 | 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/NCT02881086
GET https://conductscience.org/api/trials/v1/NCT02881086/registered