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Trial · NCT01014767

Intercontinental Multidisciplinary Registry and Treatment Optimization Study for Choroid Plexus Tumors

NCT01014767, Phase 3, Terminated, Tufts Medical Center; results first posted 2019-08-20

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Intercontinental Multidisciplinary Registry and Treatment Optimization Study for Choroid Plexus Tumors. Trials, record NCT01014767. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01014767

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Trial

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

Title
Intercontinental Multidisciplinary Registry and Treatment Optimization Study for Choroid Plexus Tumors
NCT number
NCT01014767
Status
Terminated
Phases
Phase 3
Enrollment
27 participants, actual
Lead sponsor
Tufts Medical Center
Conditions
Brain Cancer, Choroid Plexus Tumors
Interventions
Carboplatin, Cisplatin, Cyclophosphamide, Dactinomycin, Doxorubicin, Etoposide, Irinotecan, Leucovorin, Methotrexate, Temozolomide, Vincristine
First posted
2009-11-17
Last updated
2019-08-20
Results first posted
2019-08-20
Limitations and caveats
Data unavailable at sponsoring institution due to departure of PI. Data were stored and analyzed centrally at another site.

Source ClinicalTrials.gov

Registered outcomes2

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

ListOutcomeTime frameDescription
PrimaryTime to Disease ProgressionTill disease progression or death (up to 6 cycles of 28-day treatment)PI is no longer with the institution. All efforts have been exhausted to locate this data, but this data is no longer available
PrimaryToxicity During First 4 Months of Therapy4 MonthsPI is no longer with the institution. All efforts have been exhausted to locate this data, but this data is no longer available

Outcomes2

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYTime to Disease ProgressionTill disease progression or death (up to 6 cycles of 28-day treatment)PI is no longer with the institution. All efforts have been exhausted to locate this data, but this data is no longer available
PRIMARYToxicity During First 4 Months of Therapy4 MonthsPI is no longer with the institution. All efforts have been exhausted to locate this data, but this data is no longer available

Results by group0

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

None in this release.

Participant flow12

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDStandard Arm (1)12
Overall StudySTARTEDDoxorubicin/Cisplatin Arm (2)1
Overall StudySTARTEDMethotrexate Arm (3)4
Overall StudySTARTEDTemozolomide Irinotecan Arm (4)1
Overall StudyCOMPLETEDStandard Arm (1)0
Overall StudyCOMPLETEDDoxorubicin/Cisplatin Arm (2)0
Overall StudyCOMPLETEDMethotrexate Arm (3)0
Overall StudyCOMPLETEDTemozolomide Irinotecan Arm (4)0
Overall StudyNOT COMPLETEDStandard Arm (1)12
Overall StudyNOT COMPLETEDDoxorubicin/Cisplatin Arm (2)1

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 totals12

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityStandard Arm (1)00
Total, all-cause mortalityDoxorubicin/Cisplatin Arm (2)00
Total, all-cause mortalityMethotrexate Arm (3)00
Total, all-cause mortalityTemozolomide Irinotecan Arm (4)00
Total, other adverse eventsStandard Arm (1)00
Total, other adverse eventsDoxorubicin/Cisplatin Arm (2)00
Total, other adverse eventsMethotrexate Arm (3)00
Total, other adverse eventsTemozolomide Irinotecan Arm (4)00
Total, serious adverse eventsStandard Arm (1)00
Total, serious adverse eventsDoxorubicin/Cisplatin Arm (2)00

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

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/NCT01014767

GET https://conductscience.org/api/trials/v1/NCT01014767/registered