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Trial · NCT03148275

Outcomes14

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYObjective Response Rate6 monthsPercentageNUMBER
SECONDARY6 Month Progression-free Survival
From time of first dose of study medication to occurrence of radiologic tumor progression per Response Evaluation Criteria in Solid Tumors 1.1, clinical progression based on treating physician assessment or death from any cause, assessed at 6 months
percentage of participantsNUMBER
SECONDARYOverall SurvivalFrom the time of first dose of study drug to occurrence of death from any cause, assessed at 2 yearsPercentageNUMBER
SECONDARYIncidence of Adverse Eventsat 6 monthsparticipants who experienced the eventNUMBER
SECONDARYChange in Patient Reported SymptomsBaseline and at 6 monthsas participants were removed from trial, the number of completed PROMIS forms decreasedT ScoreMEAN
SECONDARYMedian Progression-free SurvivalFrom time of first dose of study medication to occurrence of radiologic tumor progression per Response Evaluation Criteria in Solid Tumors 1.1, clinical progression based on treating physicianmonthsMEDIAN
OTHER_PRE_SPECIFIEDChange in Epithelioid Hemangioendothelioma Growth RateBaseline up to 6 months
OTHER_PRE_SPECIFIEDChange in CRP LevelBaseline up to 6 months
OTHER_PRE_SPECIFIEDChange in ESR LevelBaseline up to 6 months
OTHER_PRE_SPECIFIEDChange in Plasma CTGF LevelBaseline up to 6 months
OTHER_PRE_SPECIFIEDChange in Tumor VolumeBaseline up to 6 months
OTHER_PRE_SPECIFIEDNumber of TAZ-CAMTA1 Gene FusionUp to 6 months
OTHER_PRE_SPECIFIEDPercent of TAZ-CAMTA1 Gene FusionUp to 6 months
OTHER_PRE_SPECIFIEDMAP Kinase ActivationUp to 6 months

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

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 list from software.

Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT03148275/outcomes