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Trial · NCT03172624

Study of Nivolumab Plus Ipilimumab in Patients With Salivary Gland Cancer

NCT03172624, Phase 2, Completed, Memorial Sloan Kettering Cancer Center; results first posted 2025-12-18

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Study of Nivolumab Plus Ipilimumab in Patients With Salivary Gland Cancer. Trials, record NCT03172624. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03172624

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Trial

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

Title
Study of Nivolumab Plus Ipilimumab in Patients With Salivary Gland Cancer
NCT number
NCT03172624
Status
Completed
Phases
Phase 2
Enrollment
64 participants, actual
Lead sponsor
Memorial Sloan Kettering Cancer Center
Conditions
Salivary Gland Cancer
Interventions
Nivolumab, Ipilimumab
First posted
2017-06-01
Last updated
2025-12-18
Results first posted
2025-12-18

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
PrimaryBest Overall Response Rate2 yearsusing the new international criteria proposed by the revised Response Evaluation Criteria in Solid Tumors (RECIST) guideline (version 1.1)

Outcomes1

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYBest Overall Response Rate2 yearsParticipantsCOUNT_OF_PARTICIPANTS

Results by group8

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

OutcomeGroupCategoryValueSpreadUnits
Best Overall Response RateR/M Adenoid Cystic Carcinoma (ACC)Partial Response2Participants
Best Overall Response RateR/M SGC of Any Histology, Except ACC (Non ACC)Partial Response5Participants
Best Overall Response RateR/M Adenoid Cystic Carcinoma (ACC)Stable Disease17Participants
Best Overall Response RateR/M SGC of Any Histology, Except ACC (Non ACC)Stable Disease8Participants
Best Overall Response RateR/M Adenoid Cystic Carcinoma (ACC)Progressive Disease13Participants
Best Overall Response RateR/M SGC of Any Histology, Except ACC (Non ACC)Progressive Disease18Participants
Best Overall Response RateR/M Adenoid Cystic Carcinoma (ACC)Not Evaluable0Participants
Best Overall Response RateR/M SGC of Any Histology, Except ACC (Non ACC)Not Evaluable1Participants

Participant flow6

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDR/M Adenoid Cystic Carcinoma (ACC)32
Overall StudySTARTEDR/M SGC of Any Histology, Except ACC (Non ACC)32
Overall StudyCOMPLETEDR/M Adenoid Cystic Carcinoma (ACC)32
Overall StudyCOMPLETEDR/M SGC of Any Histology, Except ACC (Non ACC)32
Overall StudyNOT COMPLETEDR/M Adenoid Cystic Carcinoma (ACC)0
Overall StudyNOT COMPLETEDR/M SGC of Any Histology, Except ACC (Non ACC)0

Adverse events114

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherAlanine aminotransferase increasedInvestigationsR/M Adenoid Cystic Carcinoma (ACC)232
otherAlanine aminotransferase increasedInvestigationsR/M SGC of Any Histology, Except ACC (Non ACC)032
otherAnemiaBlood and lymphatic system disordersR/M Adenoid Cystic Carcinoma (ACC)432
otherAnemiaBlood and lymphatic system disordersR/M SGC of Any Histology, Except ACC (Non ACC)132
otherAspartate aminotransferase increasedInvestigationsR/M Adenoid Cystic Carcinoma (ACC)432
otherAspartate aminotransferase increasedInvestigationsR/M SGC of Any Histology, Except ACC (Non ACC)232
otherHyperglycemiaMetabolism and nutrition disordersR/M Adenoid Cystic Carcinoma (ACC)032
otherHyperglycemiaMetabolism and nutrition disordersR/M SGC of Any Histology, Except ACC (Non ACC)432
otherHyponatremiaMetabolism and nutrition disordersR/M Adenoid Cystic Carcinoma (ACC)432
otherHyponatremiaMetabolism and nutrition disordersR/M SGC of Any Histology, Except ACC (Non ACC)532

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityR/M Adenoid Cystic Carcinoma (ACC)632
Total, all-cause mortalityR/M SGC of Any Histology, Except ACC (Non ACC)732
Total, other adverse eventsR/M Adenoid Cystic Carcinoma (ACC)1132
Total, other adverse eventsR/M SGC of Any Histology, Except ACC (Non ACC)1432
Total, serious adverse eventsR/M Adenoid Cystic Carcinoma (ACC)1832
Total, serious adverse eventsR/M SGC of Any Histology, Except ACC (Non ACC)932

Papers2

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
34503735DERIVEDPubMed
37620627DERIVEDPubMed

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.

ComparisonSource
R/M Adenoid Cystic Carcinoma (ACC) vs R/M SGC of Any Histology, Except ACC (Non ACC): deaths from any causeTrial comparisons
R/M Adenoid Cystic Carcinoma (ACC) vs R/M SGC of Any Histology, Except ACC (Non ACC): serious adverse eventsTrial 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.

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/NCT03172624

GET https://conductscience.org/api/trials/v1/NCT03172624/events?page=2