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Trial · NCT00507429

Study of Combretastatin and Paclitaxel/Carboplatin in the Treatment of Anaplastic Thyroid Cancer

NCT00507429, Phase 2, Phase 3, Terminated, Mateon Therapeutics; results first posted 2014-06-09

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Study of Combretastatin and Paclitaxel/Carboplatin in the Treatment of Anaplastic Thyroid Cancer. Trials, record NCT00507429. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00507429

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Trial

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

Title
Study of Combretastatin and Paclitaxel/Carboplatin in the Treatment of Anaplastic Thyroid Cancer
NCT number
NCT00507429
Status
Terminated
Phases
Phase 2, Phase 3
Enrollment
80 participants, actual
Lead sponsor
Mateon Therapeutics
Conditions
Anaplastic Thyroid Cancer
Interventions
CA4P, paclitaxel, carboplatin
First posted
2007-07-26
Last updated
2014-06-09
Results first posted
2014-06-09
Limitations and caveats
The study was to enroll 180 subjects. Enrollment was terminated early due to low accrual rate. Eighty subjects were enrolled.

Source ClinicalTrials.gov

Registered outcomes3

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

ListOutcomeTime frameDescription
PrimaryOverall SurvivalFrom randomization to date last known alive
SecondaryTo Determine Progression Free Survivalfrom randomization through end of study visit
SecondaryTo Determine Percentage of 1 Year Survivalfrom randomization through end of study visit

Outcomes3

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYOverall SurvivalFrom randomization to date last known aliveAll randomized subjects (the Intent-to-treat population) included in the analysismonthsMEDIAN
SECONDARYTo Determine Progression Free Survivalfrom randomization through end of study visit
SECONDARYTo Determine Percentage of 1 Year Survivalfrom randomization through end of study visitIntent to treatpercentage of participantsNUMBER

Results by group4

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

OutcomeGroupCategoryValueSpreadUnits
Overall SurvivalArm 1, Active: CA4P + Carboplatin + Paclitaxel5.295% Confidence Interval 3.1 to 9.0months
Overall SurvivalArm 2, Comparator: Carboplatin + Paclitaxel4.095% Confidence Interval 2.8 to 6.2months
To Determine Percentage of 1 Year SurvivalArm 1, Active: CA4P + Carboplatin + Paclitaxel26percentage of participants
To Determine Percentage of 1 Year SurvivalArm 2, Control: Carboplatin + Paclitaxel9percentage of participants

Participant flow12

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

PeriodMilestoneGroupParticipantsUnits counted
Treatment PhaseSTARTEDArm 1, Active: CA4P + Carboplatin + Paclitaxel55
Treatment PhaseSTARTEDArm 2, Control: Carboplatin + Paclitaxel25
Treatment PhaseCOMPLETEDArm 1, Active: CA4P + Carboplatin + Paclitaxel18
Treatment PhaseCOMPLETEDArm 2, Control: Carboplatin + Paclitaxel7
Treatment PhaseNOT COMPLETEDArm 1, Active: CA4P + Carboplatin + Paclitaxel37
Treatment PhaseNOT COMPLETEDArm 2, Control: Carboplatin + Paclitaxel18
Maintenance PhaseSTARTEDArm 1, Active: CA4P + Carboplatin + Paclitaxel16
Maintenance PhaseSTARTEDArm 2, Control: Carboplatin + Paclitaxel0
Maintenance PhaseCOMPLETEDArm 1, Active: CA4P + Carboplatin + Paclitaxel2
Maintenance PhaseCOMPLETEDArm 2, Control: Carboplatin + Paclitaxel0

Adverse events236

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherAbdominal painGastrointestinal disordersArm 1, Active: CA4P + Carboplatin + Paclitaxel651
otherAbdominal painGastrointestinal disordersArm 2, Comparator: Carboplatin + Paclitaxel224
otherAbdominal pain upperGastrointestinal disordersArm 1, Active: CA4P + Carboplatin + Paclitaxel451
otherAbdominal pain upperGastrointestinal disordersArm 2, Comparator: Carboplatin + Paclitaxel024
otherAlanine transferase increasedInvestigationsArm 1, Active: CA4P + Carboplatin + Paclitaxel451
otherAlanine transferase increasedInvestigationsArm 2, Comparator: Carboplatin + Paclitaxel024
otherAlopeciaSkin and subcutaneous tissue disordersArm 1, Active: CA4P + Carboplatin + Paclitaxel1651
otherAlopeciaSkin and subcutaneous tissue disordersArm 2, Comparator: Carboplatin + Paclitaxel324
otherAnemiaBlood and lymphatic system disordersArm 1, Active: CA4P + Carboplatin + Paclitaxel2051
otherAnemiaBlood and lymphatic system disordersArm 2, Comparator: Carboplatin + Paclitaxel1224

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityArm 1, Active: CA4P + Carboplatin + Paclitaxel
Total, all-cause mortalityArm 2, Comparator: Carboplatin + Paclitaxel
Total, other adverse eventsArm 1, Active: CA4P + Carboplatin + Paclitaxel5051
Total, other adverse eventsArm 2, Comparator: Carboplatin + Paclitaxel2424
Total, serious adverse eventsArm 1, Active: CA4P + Carboplatin + Paclitaxel2151
Total, serious adverse eventsArm 2, Comparator: Carboplatin + Paclitaxel524

Papers7

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
9737368BACKGROUNDPubMed
15197790BACKGROUNDPubMed
15519785BACKGROUNDPubMed
16735986BACKGROUNDPubMed
17178843BACKGROUNDPubMed
17550961BACKGROUNDPubMed
37816266DERIVEDPubMed

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 comparisons1

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

Comparison
Arm 1, Active: CA4P + Carboplatin + Paclitaxel vs Arm 2, Comparator: Carboplatin + Paclitaxel: serious adverse events

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/NCT00507429

GET https://conductscience.org/api/trials/v1/NCT00507429/events?page=2