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Trial · NCT02819843

A Study of T-VEC (Talimogene Laherparepvec) With or Without Radiotherapy for Melanoma, Merkel Cell Carcinoma, or Other Solid Tumors

NCT02819843, Phase 2, Completed, Memorial Sloan Kettering Cancer Center; results first posted 2025-01-29

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. A Study of T-VEC (Talimogene Laherparepvec) With or Without Radiotherapy for Melanoma, Merkel Cell Carcinoma, or Other Solid Tumors. Trials, record NCT02819843. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02819843

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Trial

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

Title
A Study of T-VEC (Talimogene Laherparepvec) With or Without Radiotherapy for Melanoma, Merkel Cell Carcinoma, or Other Solid Tumors
NCT number
NCT02819843
Status
Completed
Phases
Phase 2
Enrollment
19 participants, actual
Lead sponsor
Memorial Sloan Kettering Cancer Center
Conditions
Melanoma, Merkel Cell Carcinoma, Other Solid Tumors
Interventions
TALIMOGENE LAHERPAREPVEC (TVEC), Hypofractionated Radiotherapy
First posted
2016-06-30
Last updated
2025-01-29
Results first posted
2025-01-29

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
PrimaryBest Response16 weeks
Overall subject level response is defined as partial or complete (\>50% or greater decrease in largest lesion) by the modified World Health Organization (mWHO) criteria, and will include measurements of tumor size by CT component of PET/CT, and clinically by digital photography.

Outcomes1

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYBest Response16 weeksParticipantsCOUNT_OF_PARTICIPANTS

Results by group8

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

OutcomeGroupCategoryValueSpreadUnits
Best ResponseIntralesional TALIMOGENE LAHERPAREPVEC Without RadiotherapyComplete Response1Participants
Best ResponseIntralesional TALIMOGENE LAHERPAREPVEC With RadiotherapyComplete Response1Participants
Best ResponseIntralesional TALIMOGENE LAHERPAREPVEC Without RadiotherapyPartial Response0Participants
Best ResponseIntralesional TALIMOGENE LAHERPAREPVEC With RadiotherapyPartial Response0Participants
Best ResponseIntralesional TALIMOGENE LAHERPAREPVEC Without RadiotherapyStable Disease2Participants
Best ResponseIntralesional TALIMOGENE LAHERPAREPVEC With RadiotherapyStable Disease5Participants
Best ResponseIntralesional TALIMOGENE LAHERPAREPVEC Without RadiotherapyProgressive Disease6Participants
Best ResponseIntralesional TALIMOGENE LAHERPAREPVEC With RadiotherapyProgressive Disease4Participants

Participant flow6

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDIntralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy9
Overall StudySTARTEDIntralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy10
Overall StudyCOMPLETEDIntralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy9
Overall StudyCOMPLETEDIntralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy9
Overall StudyNOT COMPLETEDIntralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy0
Overall StudyNOT COMPLETEDIntralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy1

Adverse events20

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherFeverGeneral disordersIntralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy59
otherFeverGeneral disordersIntralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy310
otherFatigueGeneral disordersIntralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy29
otherFatigueGeneral disordersIntralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy310
otherChillsGeneral disordersIntralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy29
otherChillsGeneral disordersIntralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy510
otherVomitingGastrointestinal disordersIntralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy19
otherVomitingGastrointestinal disordersIntralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy110
otherDyspneaRespiratory, thoracic and mediastinal disordersIntralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy09
otherDyspneaRespiratory, thoracic and mediastinal disordersIntralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy110

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityIntralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy89
Total, all-cause mortalityIntralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy910
Total, other adverse eventsIntralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy99
Total, other adverse eventsIntralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy1010
Total, serious adverse eventsIntralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy09
Total, serious adverse eventsIntralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy010

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 comparisons2

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

ComparisonSource
Intralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy vs Intralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy: deaths from any causeTrial comparisons
Intralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy vs Intralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy: serious adverse eventsTrial comparisons

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/NCT02819843

GET https://conductscience.org/api/trials/v1/NCT02819843/registered