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Trial · NCT02383433

Regorafenib Plus Gemcitabine in Metastatic Pancreatic Cancer

NCT02383433, Phase 2, Terminated, Case Comprehensive Cancer Center; results first posted 2019-05-10

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Regorafenib Plus Gemcitabine in Metastatic Pancreatic Cancer. Trials, record NCT02383433. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02383433

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Trial

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

Title
Regorafenib Plus Gemcitabine in Metastatic Pancreatic Cancer
NCT number
NCT02383433
Status
Terminated
Phases
Phase 2
Enrollment
2 participants, actual
Lead sponsor
Case Comprehensive Cancer Center
Conditions
Metastatic Pancreatic Adenocarcinoma
Interventions
Regorafenib, Gemcitabine Hydrochloride
First posted
2015-03-09
Last updated
2023-10-23
Results first posted
2019-05-10
Limitations and caveats
Data was not collected, study terminated early due to low accrual.

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
PrimaryProgression-free SurvivalUp to 1 year from enrollmentTime-to-event data will be summarized using the Kaplan-Meier method.

Outcomes1

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYProgression-free SurvivalUp to 1 year from enrollmentData was not collected for this outcome, study terminated early due to low accrual.

Results by group0

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

None in this release.

Participant flow3

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDTreatment (Regorafenib, Gemcitabine Hydrochloride)2
Overall StudyCOMPLETEDTreatment (Regorafenib, Gemcitabine Hydrochloride)0
Overall StudyNOT COMPLETEDTreatment (Regorafenib, Gemcitabine Hydrochloride)2

Adverse events52

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherAbdominal PainGastrointestinal disordersTreatment (Regorafenib, Gemcitabine Hydrochloride)121
otherAlkaline phosphatase increasedInvestigationsTreatment (Regorafenib, Gemcitabine Hydrochloride)122
otheralkaline phosphatase, increased gr1InvestigationsTreatment (Regorafenib, Gemcitabine Hydrochloride)121
otherALT increasedInvestigationsTreatment (Regorafenib, Gemcitabine Hydrochloride)128
otherALT increased, gr1InvestigationsTreatment (Regorafenib, Gemcitabine Hydrochloride)121
otherAnorexiaMetabolism and nutrition disordersTreatment (Regorafenib, Gemcitabine Hydrochloride)121
otherAspartate Aminotransferase IncreasedInvestigationsTreatment (Regorafenib, Gemcitabine Hydrochloride)121
otherAST increasedInvestigationsTreatment (Regorafenib, Gemcitabine Hydrochloride)121
otherColitisGastrointestinal disordersTreatment (Regorafenib, Gemcitabine Hydrochloride)121
otherdecreased plateletsInvestigationsTreatment (Regorafenib, Gemcitabine Hydrochloride)121

Adverse event totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityTreatment (Regorafenib, Gemcitabine Hydrochloride)22
Total, other adverse eventsTreatment (Regorafenib, Gemcitabine Hydrochloride)22
Total, serious adverse eventsTreatment (Regorafenib, Gemcitabine Hydrochloride)22

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants1

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.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal years
P30CA043703Case Comprehensive Cancer Center Support GrantSCHWARTZ, GARY KCASE WESTERN RESERVE UNIVERSITYNATIONAL CANCER INSTITUTE1987 to 2025

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/NCT02383433

GET https://conductscience.org/api/trials/v1/NCT02383433/events?page=2