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Trial · NCT02364076

Pembrolizumab and Epacadostat in Patients With Thymic Carcinoma

NCT02364076, Phase 2, Unknown, Georgetown University; results first posted 2019-12-13

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Pembrolizumab and Epacadostat in Patients With Thymic Carcinoma. Trials, record NCT02364076. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02364076

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Trial

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

Title
Pembrolizumab and Epacadostat in Patients With Thymic Carcinoma
NCT number
NCT02364076
Status
Unknown
Phases
Phase 2
Enrollment
45 participants, actual
Lead sponsor
Georgetown University
Conditions
Thymic Carcinoma, Thymus Neoplasms, Thymus Cancer
Interventions
Pembrolizumab, Epacadostat
First posted
2015-02-16
Last updated
2019-12-13
Results first posted
2019-12-13

Source ClinicalTrials.gov

Registered outcomes4

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

ListOutcomeTime frameDescription
PrimaryResponse Rate24 monthsTo measure response of all the participants to the drug at the end of the study.
SecondaryProgression-free Survival24 monthsTime between start of treatment and tumor progression or death
SecondaryOverall Survival24 monthsTime between start of treatment and death
SecondaryNumber of Participants With New-Onset Severe Adverse Events24 months

Outcomes4

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYResponse Rate24 monthsParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYProgression-free Survival24 monthsmonthsMEDIAN
SECONDARYOverall Survival24 monthsmonthsMEDIAN
SECONDARYNumber of Participants With New-Onset Severe Adverse Events24 monthsParticipantsCOUNT_OF_PARTICIPANTS

Results by group7

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

OutcomeGroupCategoryValueSpreadUnits
Response RatePembrolizumabComplete Response1Participants
Response RatePembrolizumabPartial response8Participants
Response RatePembrolizumabStable Disease21Participants
Response RatePembrolizumabProgression10Participants
Progression-free SurvivalPembrolizumab4.295% Confidence Interval 2.9 to 10.3months
Overall SurvivalPembrolizumab24.995% Confidence Interval 15.5 to NAmonths
Number of Participants With New-Onset Severe Adverse EventsPembrolizumab6Participants

Participant flow3

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDPembrolizumab and Epacadostat45
Overall StudyCOMPLETEDPembrolizumab and Epacadostat40
Overall StudyNOT COMPLETEDPembrolizumab and Epacadostat5

Adverse events39

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherFatigueGeneral disordersPembrolizumab and Epacadostat1640
otherDyspneaRespiratory, thoracic and mediastinal disordersPembrolizumab and Epacadostat340
otherhypothyroidismEndocrine disordersPembrolizumab and Epacadostat540
otherhypokalemiaMetabolism and nutrition disordersPembrolizumab and Epacadostat140
otherElevated alkaline phosphataseMetabolism and nutrition disordersPembrolizumab and Epacadostat1040
othermyocarditisCardiac disordersPembrolizumab and Epacadostat240
otherAST elevationMetabolism and nutrition disordersPembrolizumab and Epacadostat1640
otherFlu likeGeneral disordersPembrolizumab and Epacadostat240
otherALT increasedHepatobiliary disordersPembrolizumab and Epacadostat1040
otherDiarrhoeaGastrointestinal disordersPembrolizumab and Epacadostat940

Adverse event totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityPembrolizumab and Epacadostat1740
Total, other adverse eventsPembrolizumab and Epacadostat4040
Total, serious adverse eventsPembrolizumab and Epacadostat640

Papers2

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
29395863DERIVEDPubMed
34622229DERIVEDPubMed

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/NCT02364076

GET https://conductscience.org/api/trials/v1/NCT02364076/events?page=2