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Trial · NCT00412542

Thalidomide and Temozolomide or Camptothecin-11 (CPT-11) in Patients With Gliomas

NCT00412542, Phase 2, Completed, M.D. Anderson Cancer Center; results first posted 2012-02-28

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Thalidomide and Temozolomide or Camptothecin-11 (CPT-11) in Patients With Gliomas. Trials, record NCT00412542. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00412542

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Trial

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

Title
Thalidomide and Temozolomide or Camptothecin-11 (CPT-11) in Patients With Gliomas
NCT number
NCT00412542
Status
Completed
Phases
Phase 2
Enrollment
78 participants, actual
Lead sponsor
M.D. Anderson Cancer Center
Conditions
Glioblastoma Multiforme, Glioma
Interventions
Thalidomide, CPT-11, MRI Scan, Quantitative Sensory Tests (QST)
First posted
2006-12-18
Last updated
2012-02-28
Results first posted
2012-02-28

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
PrimaryNumber of Participants Progression Free at 6 Months With Malignant Gliomas6 MonthsProgression-free Survival (PFS) measured as number of participants that are alive and progression-free at 6 months.

Outcomes1

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYNumber of Participants Progression Free at 6 Months With Malignant Gliomas6 Months7 participants enrolled were not evaluated as they were evaluable for toxicity only (not having completed the first cycle/clinical decline/etc.).participantsNUMBER

Results by group1

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

OutcomeGroupCategoryValueSpreadUnits
Number of Participants Progression Free at 6 Months With Malignant GliomasParticipants With Recurrent Malignant Gliomas24participants

Participant flow6

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDGlioblastoma Multiforme: Thalidomide + CPT-1133
Overall StudySTARTEDAnaplastic Gliomas: Thalidomide + CPT-1145
Overall StudyCOMPLETEDGlioblastoma Multiforme: Thalidomide + CPT-1133
Overall StudyCOMPLETEDAnaplastic Gliomas: Thalidomide + CPT-1142
Overall StudyNOT COMPLETEDGlioblastoma Multiforme: Thalidomide + CPT-110
Overall StudyNOT COMPLETEDAnaplastic Gliomas: Thalidomide + CPT-113

Adverse events119

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherAbdominal crampingGastrointestinal disordersPatients With Recurrent Malignant Gliomas97518
otherAcneSkin and subcutaneous tissue disordersPatients With Recurrent Malignant Gliomas127517
otherAlkaline Phosphatase increasedInvestigationsPatients With Recurrent Malignant Gliomas117518
otherAllergic rhinitisRespiratory, thoracic and mediastinal disordersPatients With Recurrent Malignant Gliomas117516
otherAlopeciaSkin and subcutaneous tissue disordersPatients With Recurrent Malignant Gliomas137513
otherALT increasedInvestigationsPatients With Recurrent Malignant Gliomas177540
otherAnemiaBlood and lymphatic system disordersPatients With Recurrent Malignant Gliomas57511
otherAnorexiaGastrointestinal disordersPatients With Recurrent Malignant Gliomas227525
otherAST elevatedInvestigationsPatients With Recurrent Malignant Gliomas127519
otherAtaxiaNervous system disordersPatients With Recurrent Malignant Gliomas6759

Adverse event totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityPatients With Recurrent Malignant Gliomas
Total, other adverse eventsPatients With Recurrent Malignant Gliomas6575
Total, serious adverse eventsPatients With Recurrent Malignant Gliomas3575

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/NCT00412542

GET https://conductscience.org/api/trials/v1/NCT00412542/events?page=2