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Trial · NCT02759575

A Study of Chemoradiation Plus Pembrolizumab for Locally Advanced Laryngeal Squamous Cell Carcinoma

NCT02759575, Phase 1, Phase 2, Completed, Vinita Takiar; results first posted 2021-03-12

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. A Study of Chemoradiation Plus Pembrolizumab for Locally Advanced Laryngeal Squamous Cell Carcinoma. Trials, record NCT02759575. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02759575

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Trial

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

Title
A Study of Chemoradiation Plus Pembrolizumab for Locally Advanced Laryngeal Squamous Cell Carcinoma
NCT number
NCT02759575
Status
Completed
Phases
Phase 1, Phase 2
Enrollment
9 participants, actual
Lead sponsor
Vinita Takiar
Conditions
Head and Neck Cancer
Interventions
Pembrolizumab, Radiation Therapy, Cisplatin
First posted
2016-05-03
Last updated
2021-03-12
Results first posted
2021-03-12

Source ClinicalTrials.gov

Registered outcomes3

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

ListOutcomeTime frameDescription
PrimaryNumber of Participants With Treatment-Related Grade 3 or 4 Adverse Events as Assessed by CTCAE V4.030 days following completion of treatment for the first 6 participantsGreater than 2 grade 3 or 4 adverse events that are definitely, probably or possibly related to the pembrolizumab in the first cohort of 6 participants
PrimaryLaryngectomy-free Survival in Locally Advanced Laryngeal Squamous Cell Carcinoma18 monthsThis is the number of subjects that are laryngectomy-free at 18 months.
SecondaryLaryngectomy-free Survival in Locally Advanced Laryngeal Squamous Cell Carcinoma12 monthsThis is the number of subjects that are laryngectomy-free at 12 months.

Outcomes3

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYNumber of Participants With Treatment-Related Grade 3 or 4 Adverse Events as Assessed by CTCAE V4.030 days following completion of treatment for the first 6 participantsThese are the first six participants that completed the study.ParticipantsCOUNT_OF_PARTICIPANTS
PRIMARYLaryngectomy-free Survival in Locally Advanced Laryngeal Squamous Cell Carcinoma18 monthsParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYLaryngectomy-free Survival in Locally Advanced Laryngeal Squamous Cell Carcinoma12 monthsParticipantsCOUNT_OF_PARTICIPANTS

Results by group3

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

OutcomeGroupCategoryValueSpreadUnits
Number of Participants With Treatment-Related Grade 3 or 4 Adverse Events as Assessed by CTCAE V4.0Pembrolizumab2Participants
Laryngectomy-free Survival in Locally Advanced Laryngeal Squamous Cell CarcinomaPembrolizumab9Participants
Laryngectomy-free Survival in Locally Advanced Laryngeal Squamous Cell CarcinomaPembrolizumab9Participants

Participant flow3

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDPembrolizumab9
Overall StudyCOMPLETEDPembrolizumab9
Overall StudyNOT COMPLETEDPembrolizumab0

Adverse events87

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherAcute Kidney InjuryRenal and urinary disordersPembrolizumab496
otherAnemiaBlood and lymphatic system disordersPembrolizumab395
otherAnxietyPsychiatric disordersPembrolizumab393
otherArthralgiaMusculoskeletal and connective tissue disordersPembrolizumab191
otherColitisGastrointestinal disordersPembrolizumab191
otherConstipationGastrointestinal disordersPembrolizumab394
otherCoughRespiratory, thoracic and mediastinal disordersPembrolizumab494
otherCreatinine increasedInvestigationsPembrolizumab192
otherDehydrationMetabolism and nutrition disordersPembrolizumab394
otherDermatitis radiationInjury, poisoning and procedural complicationsPembrolizumab9912

Adverse event totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityPembrolizumab39
Total, other adverse eventsPembrolizumab99
Total, serious adverse eventsPembrolizumab39

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
35434343DERIVED

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/NCT02759575

GET https://conductscience.org/api/trials/v1/NCT02759575/events?page=2