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
Cite this record
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
On this page
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.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Best Response | 16 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. |
Source ClinicalTrials.gov
Outcomes1
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Best Response | 16 weeks | Participants | COUNT_OF_PARTICIPANTS |
Source ClinicalTrials.gov
Results by group8
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Best Response | Intralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy | Complete Response | 1 | Participants | |
| Best Response | Intralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy | Complete Response | 1 | Participants | |
| Best Response | Intralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy | Partial Response | 0 | Participants | |
| Best Response | Intralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy | Partial Response | 0 | Participants | |
| Best Response | Intralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy | Stable Disease | 2 | Participants | |
| Best Response | Intralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy | Stable Disease | 5 | Participants | |
| Best Response | Intralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy | Progressive Disease | 6 | Participants | |
| Best Response | Intralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy | Progressive Disease | 4 | Participants |
Source ClinicalTrials.gov
Participant flow6
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted |
|---|---|---|---|---|
| Overall Study | STARTED | Intralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy | 9 | |
| Overall Study | STARTED | Intralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy | 10 | |
| Overall Study | COMPLETED | Intralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy | 9 | |
| Overall Study | COMPLETED | Intralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy | 9 | |
| Overall Study | NOT COMPLETED | Intralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy | 0 | |
| Overall Study | NOT COMPLETED | Intralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy | 1 |
Source ClinicalTrials.gov
Adverse events20
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events |
|---|---|---|---|---|---|---|
| other | Fever | General disorders | Intralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy | 5 | 9 | |
| other | Fever | General disorders | Intralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy | 3 | 10 | |
| other | Fatigue | General disorders | Intralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy | 2 | 9 | |
| other | Fatigue | General disorders | Intralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy | 3 | 10 | |
| other | Chills | General disorders | Intralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy | 2 | 9 | |
| other | Chills | General disorders | Intralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy | 5 | 10 | |
| other | Vomiting | Gastrointestinal disorders | Intralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy | 1 | 9 | |
| other | Vomiting | Gastrointestinal disorders | Intralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy | 1 | 10 | |
| other | Dyspnea | Respiratory, thoracic and mediastinal disorders | Intralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy | 0 | 9 | |
| other | Dyspnea | Respiratory, thoracic and mediastinal disorders | Intralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy | 1 | 10 |
1 to 10 of 20Source ClinicalTrials.gov
See all 20 adverse eventsAdverse event totals6
The totals the trial posted for each group.
| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | Intralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy | 8 | 9 |
| Total, all-cause mortality | Intralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy | 9 | 10 |
| Total, other adverse events | Intralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy | 9 | 9 |
| Total, other adverse events | Intralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy | 10 | 10 |
| Total, serious adverse events | Intralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy | 0 | 9 |
| Total, serious adverse events | Intralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy | 0 | 10 |
Source ClinicalTrials.gov
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.
| Comparison | Source |
|---|---|
| Intralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy vs Intralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy: deaths from any cause | Trial comparisons |
| Intralesional TALIMOGENE LAHERPAREPVEC Without Radiotherapy vs Intralesional TALIMOGENE LAHERPAREPVEC With Radiotherapy: serious adverse events | Trial 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.
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