ConductScience.org, home

Trial · NCT03663712

Talimogene Laherparepvec for the Treatment of Peritoneal Surface Malignancies

NCT03663712, Phase 1, Completed, Dan Blazer III, M.D.; results first posted 2024-11-20

3 sourcestrials-2026-11-12-0.5.0

Download JSON
Cite this record

ConductScience Library. Talimogene Laherparepvec for the Treatment of Peritoneal Surface Malignancies. Trials, record NCT03663712. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03663712

On this page

Trial

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

Title
Talimogene Laherparepvec for the Treatment of Peritoneal Surface Malignancies
NCT number
NCT03663712
Status
Completed
Phases
Phase 1
Enrollment
28 participants, actual
Lead sponsor
Dan Blazer III, M.D.
Conditions
Peritoneal Surface Malignancy
Interventions
Talimogene Laherparepvec
First posted
2018-09-10
Last updated
2024-11-20
Results first posted
2024-11-20

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
PrimaryDose Limiting Toxicity (DLT)from start of treatment until 30-day follow-up visit, up to 14 weeksNumber of participants who experienced a dose limiting toxicity (DLT)

Outcomes1

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYDose Limiting Toxicity (DLT)from start of treatment until 30-day follow-up visit, up to 14 weeksParticipantsCOUNT_OF_PARTICIPANTS

Results by group3

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

OutcomeGroupCategoryValueSpreadUnits
Dose Limiting Toxicity (DLT)TVEC Dose of 4x10^6 PFU (Plaque-forming Units)0Participants
Dose Limiting Toxicity (DLT)TVEC Dose of 4x10^7 PFU (Plaque-forming Units)0Participants
Dose Limiting Toxicity (DLT)TVEC Dose of 4x10^8 PFU (Plaque-forming Units)0Participants

Participant flow9

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDDose Level 13
Overall StudySTARTEDDose Level 24
Overall StudySTARTEDDose Level 311
Overall StudyCOMPLETEDDose Level 13
Overall StudyCOMPLETEDDose Level 24
Overall StudyCOMPLETEDDose Level 311
Overall StudyNOT COMPLETEDDose Level 10
Overall StudyNOT COMPLETEDDose Level 20
Overall StudyNOT COMPLETEDDose Level 30

Adverse events63

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherAnemiaBlood and lymphatic system disordersDose Level 103
otherAnemiaBlood and lymphatic system disordersDose Level 204
otherAnemiaBlood and lymphatic system disordersDose Level 3211
otherAbdominal painGastrointestinal disordersDose Level 123
otherAbdominal painGastrointestinal disordersDose Level 214
otherAbdominal painGastrointestinal disordersDose Level 3811
otherConstipationGastrointestinal disordersDose Level 113
otherConstipationGastrointestinal disordersDose Level 204
otherConstipationGastrointestinal disordersDose Level 3111
otherNauseaGastrointestinal disordersDose Level 103

Adverse event totals9

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityDose Level 133
Total, all-cause mortalityDose Level 244
Total, all-cause mortalityDose Level 3511
Total, other adverse eventsDose Level 133
Total, other adverse eventsDose Level 234
Total, other adverse eventsDose Level 31011
Total, serious adverse eventsDose Level 113
Total, serious adverse eventsDose Level 224
Total, serious adverse eventsDose Level 3311

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 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/NCT03663712

GET https://conductscience.org/api/trials/v1/NCT03663712/events?page=2