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Trial · NCT03211988

Entinostat Neuroendocrine (NE) Tumor

NCT03211988, Phase 2, Terminated, Antonio Fojo; results first posted 2026-03-02

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Entinostat Neuroendocrine (NE) Tumor. Trials, record NCT03211988. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03211988

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Trial

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

Title
Entinostat Neuroendocrine (NE) Tumor
NCT number
NCT03211988
Status
Terminated
Phases
Phase 2
Enrollment
5 participants, actual
Lead sponsor
Antonio Fojo
Conditions
Neuroendocrine Tumors
Interventions
Entinostat
First posted
2017-07-11
Last updated
2026-03-02
Results first posted
2026-03-02

Source ClinicalTrials.gov

Registered outcomes4

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

ListOutcomeTime frameDescription
PrimaryObjective Response Rate (ORR)Up to 44 months
Objective response defined as complete response (CR) (Disappearance of all target lesions. Any pathological lymph nodes (whether target or non-target) must have reduction in short axis to \<10 mm.) and partial response (PR) (at least a 30% decrease in the sum of diameters of target lesions, taking as reference the baseline sum diameters) and will be determined from each participant's best confirmed response during protocol therapy. Response as evaluated per RECIST 1.1 criteria.
SecondaryDuration of Progression-Free Survival (PFS)Up to 45 monthsTime from study enrollment until disease progression or death.
SecondaryDuration of Overall Survival (OS)Up to 45 monthsThe length of time from either the date of diagnosis or start of treatment that years participants diagnosed with the disease are still alive.
SecondaryDuration of Response for Participants Who Achieve Complete Response (CR) or Partial Response (PR)Up to 4 yearsTime from documentation of tumor response to disease progression in participants who achieve CR or PR.

Outcomes4

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYObjective Response Rate (ORR)Up to 44 monthsParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYDuration of Progression-Free Survival (PFS)Up to 45 monthsdaysMEDIAN
SECONDARYDuration of Overall Survival (OS)Up to 45 monthsdaysMEDIAN
SECONDARYDuration of Response for Participants Who Achieve Complete Response (CR) or Partial Response (PR)Up to 4 yearsZero analyzed as there were no participants that achieved CR or PR.

Results by group3

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

OutcomeGroupCategoryValueSpreadUnits
Objective Response Rate (ORR)Entinostat0Participants
Duration of Progression-Free Survival (PFS)Entinostat381Full Range 232 to 754days
Duration of Overall Survival (OS)Entinostat1422Full Range 1163 to 1611days

Participant flow3

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDEntinostat5
Overall StudyCOMPLETEDEntinostat4
Overall StudyNOT COMPLETEDEntinostat1

Adverse events26

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherAbdominal PainGastrointestinal disordersEntinostat15
otherHypophosphatemiaMetabolism and nutrition disordersEntinostat15
otherHyperkalemiaMetabolism and nutrition disordersEntinostat15
otherVomitingGastrointestinal disordersEntinostat35
otherAnorexiaMetabolism and nutrition disordersEntinostat25
otherBloatingGastrointestinal disordersEntinostat15
otherFatigueGeneral disordersEntinostat35
otherNauseaGastrointestinal disordersEntinostat45
otherUrinary tract painRenal and urinary disordersEntinostat15
otherNeutrophil count decreasedInvestigationsEntinostat45

Adverse event totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityEntinostat15
Total, other adverse eventsEntinostat55
Total, serious adverse eventsEntinostat15

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
38886159DERIVED

Source PubMed

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/NCT03211988

GET https://conductscience.org/api/trials/v1/NCT03211988/events?page=2