RecruitingPhase 2NCT06302569

Pembrolizumab Plus Enfortumab Vedotin in Collecting Duct and Renal Medullary Carcinoma

Activity of Pembrolizumab Plus Enfortumab Vedotin in Collecting Duct and Renal Medullary Carcinoma


Sponsor

Giuseppe Procopio

Enrollment

23 participants

Start Date

May 30, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This is a single-arm, monocentric, phase II trial, enrolling patients with histological diagnosis of collecting duct carcinoma and renal medullary carcinoma with locally advanced or metastatic disease who will be treated with Pembrolizumab plus Enfortumab Vedotin. Approximately, 23 patients will be enrolled. At screening, pre-existing archival primary and metastatic FFPE tumor specimen will be collected and submitted for central pathology review and translational analysis. All participants will undergo baseline screening imaging for clinical staging. Patients will be treated with Pembrolizumab q21 plus Enfortumab Vedotin 1,8q21 for 3 cycles (3 infusion of Pembrolizumab and 6 infusion of Enfortumab Vedotin) then radiological imaging will be repeated and patients with SD, PR or CR will continue pembrolizumab until disease progression, unacceptable toxicities or completion of treatment (17 cycles). Patients with progressive disease after 3 cycles of study intervention will be treated as per clinical practice. Patients who will experience progressive disease during pembrolizumab monotherapy treatment could restart Enfortumab Vedotin. The study will also involve collection of a blood sample taken at the commencement of treatment, at the first cycle, after cycle 3 and at the end of treatment or progression of disease, to be used for research purposes.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests a combination of two cancer drugs — pembrolizumab (an immunotherapy) and enfortumab vedotin (a targeted antibody-drug) — in people with rare and aggressive forms of kidney cancer: collecting duct carcinoma and medullary renal cell carcinoma. These cancers are very uncommon and have limited treatment options. **You may be eligible if...** - You are 18 years or older - You have confirmed collecting duct carcinoma or medullary renal cell carcinoma that is advanced or has spread - Your cancer can be measured on imaging - You have tumor tissue available for testing - You are in good general health (ECOG score acceptable per protocol) **You may NOT be eligible if...** - You have a different type of kidney cancer - You have serious autoimmune conditions that are not well-controlled - You are pregnant or breastfeeding - You have active or uncontrolled infections Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGPembrolizumab + Enfortumab Vedotin

* Pembrolizumab will be given for a maximum of 2 years i.e. a total of 35 cycles of pembrolizumab with the q3 week dosing. Participants who complete study intervention after 2 years of pembrolizumab are eligible for up to 1 year of additional pembrolizumab (second course) upon experiencing disease progression. * Enfortumab Vedotin will be given for a maximum of 3 cycles on day 1 and day 3 each 3 weeks. EV treatment could be re-started in case of Progressive Disease RECIST v1.1 during pembrolizumab monotherapy treatment.


Locations(1)

Fondazione Irccs Istituto Dei Tumori Di Milano

Milan, Italy

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NCT06302569


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