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Immunotherapy and Irreversible Electroporation (IRE) in the Treatment of Locally Advanced Pancreatic Adenocarcinoma

NCT07930936, Phase 1, Not yet recruiting, Robert C. Martin

Trial 10

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

FieldValueSource
TitleImmunotherapy and Irreversible Electroporation (IRE) in the Treatment of Locally Advanced Pancreatic AdenocarcinomaClinicalTrials.gov
NCT numberNCT07930936ClinicalTrials.gov
StatusNot yet recruitingClinicalTrials.gov
PhasesPhase 1ClinicalTrials.gov
Enrollment10 participants, estimatedClinicalTrials.gov
Lead sponsorRobert C. MartinClinicalTrials.gov
ConditionsLocally Advanced Pancreatic AdenocarcinomaClinicalTrials.gov
Interventions1.0% IP-001 for injection, Irreversible ElectroporationClinicalTrials.gov
First posted2026-11-12ClinicalTrials.gov
Last updated2026-11-12ClinicalTrials.gov

Registered outcomes 2

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

ListOutcomeTime frameDescriptionSource
PrimarySafety and tolerability of IP-001 administered intratumorally following IREDay 0 to 90 days after treatment or the start of subsequent anti-cancer therapy, whichever comes firstIncidence, severity, and outcomes of adverse events assessed by CTCAE v4.0, clinical assessments, and laboratory test abnormalities, as well as a return to baseline patient reported outcomes.ClinicalTrials.gov
SecondaryProgression Free SurvivalMonths 12 and 24
Assessed from Treatment Day 0 to the first documented occurrence of progression (local or distant) or death, whichever comes first. Progression will be determined by the investigator's radiological review per RECIST v1.1
ClinicalTrials.gov

Outcomes 0

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

TypeOutcomeTime framePopulationUnitsMeasured asSource

Results by group 0

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

OutcomeGroupCategoryValueSpreadUnitsSource

Participant flow 0

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

PeriodMilestoneGroupParticipantsUnits countedSource

Adverse events 0

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

TypeEventOrgan systemGroupAffectedAt riskEventsSource

Adverse event totals 0

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource

Papers 0

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource

Trial comparisons 0

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

ComparisonSource

Tests 0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource

Source 4

FieldValueSource
Releasetrials-2026-11-12-0.3.0ClinicalTrials.gov
Release manifest SHA-2564a570df2e7274cee2d4fa2959402fab41880e2cd412e4b590390035fbea69391ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov

The same record as JSON

Release trials-2026-11-12-0.3.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.