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Trial · NCT06302569

Pembrolizumab Plus Enfortumab Vedotin in Collecting Duct and Renal Medullary Carcinoma

NCT06302569, Phase 2, Recruiting, Giuseppe Procopio

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Pembrolizumab Plus Enfortumab Vedotin in Collecting Duct and Renal Medullary Carcinoma. Trials, record NCT06302569. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06302569

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Trial

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

Title
Pembrolizumab Plus Enfortumab Vedotin in Collecting Duct and Renal Medullary Carcinoma
NCT number
NCT06302569
Status
Recruiting
Phases
Phase 2
Enrollment
23 participants, estimated
Lead sponsor
Giuseppe Procopio
Conditions
Bellini Carcinoma, Collecting Duct Carcinoma, Renal Medullary Carcinoma
Interventions
Pembrolizumab + Enfortumab Vedotin
First posted
2024-03-08
Last updated
2025-09-09

Source ClinicalTrials.gov

Registered outcomes4

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

ListOutcomeTime frameDescription
PrimaryORR in patients treated with Pembrolizumab plus Enfortumab Vedotin24 MonthsThe proportion of patients who have a partial or complete response to Pembrolizumab + Enfortumab Vedotin
SecondaryProgression-free survival (PFS) in patients treated with Pembrolizumab plus Enfortumab Vedotin24 MonthsThe time from assignment to Pembrolizumab plus Enfortumab Vedotin to disease progression or death from any cause
SecondaryOverall-survival (OS) in patients treated with Pembrolizumab plus Enfortumab Vedotin48 MonthsSurvival from assignment to Pembrolizumab plus Enfortumab Vedotin to time of death.
SecondaryNumber of Participants treated with Pembrolizumab + Enfortumab Vedotin who experience AEs/SAEs24 MonthsThe incidence of, causality, and outcome of AEs/SAEs. AEs will be assessed as defined by CTCAE, Version \[5.0\].

Outcomes0

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

None in this release.

Results by group0

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

None in this release.

Participant flow0

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

None in this release.

Adverse events0

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

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers20

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
11282341RESULTPubMed
11698646RESULTPubMed
15771580RESULTPubMed
15800326RESULTPubMed
16227604RESULTPubMed
17437788RESULTPubMed
17474988RESULTPubMed
17928952RESULTPubMed
18565862RESULTPubMed
18593353RESULTPubMed

1 to 10 of 20

See all 20 papers

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/NCT06302569

GET https://conductscience.org/api/trials/v1/NCT06302569/registered