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Taking people in PolandPhase 3

Tests casdatifan with cabozantinib in advanced kidney cancer

Tests casdatifan plus cabozantinib against placebo in adults with advanced clear cell kidney cancer.

Plain-language title generated from the registry record
Registry title: Study of Casdatifan and Cabozantinib Versus Placebo and Cabozantinib in Patients With Advanced Clear Cell Renal Cell Carcinoma

Key facts

Where
Bielsko-Biala, Cracow, Koszalin, Otwock, Poznan, Rzeszow, Siedlce, Skorzewo, Tomaszow Mazowiecki, Warsaw, and Wroclaw, PolandSee the 12 sites
Phase
Phase 3

Where in Poland

  • Beskidzkie Centrum Onkologii Szpital Miejski Im. Jana Pawla II W Bielsku-Bialej SPZOZBielsko-Biala, PolandTaking people
  • Pratia S.A.Cracow, PolandTaking people
  • Szpital Wojewodzki im. Mikolaja Kopernika w KoszalinieKoszalin, PolandTaking people
  • Europejskie Centrum Zdrowia Otwock Sp. Z.o.o.Otwock, PolandTaking people
  • Med Polonia Sp z o.o.Poznan, PolandTaking people
  • Pratia S.A.Poznan, PolandTaking people
  • Centrum Medyczne Medyk Sp. z o.o. S.K.Rzeszow, PolandTaking people
  • Mazowiecki Szpital Wojewodzki Im. Sw. Jana Pawła II W Siedlcach Sp. z o.o.Siedlce, PolandTaking people
  • Aidport sp z o.o.Skorzewo, PolandTaking people
  • Provita Centrum Medyczne Sp. z o.o.Tomaszow Mazowiecki, PolandTaking people
  • MTZ Clinical Research powered by PratiaWarsaw, PolandTaking people
  • Pratia S.A.Wroclaw, PolandTaking people

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  2. Are travel costs paid?
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  4. What happens if I want to stop?
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Trial details

Who runs it
Arcus Biosciences, Inc.
Trial code
NCT07011719EU 2024-515023-11-00
Record updated
2 November 2026
Original description
The purpose of the study is to evaluate the progression-free survival (PFS) of casdatifan versus placebo when each is given in combination with cabozantinib for patients who received anti-PD-1 or anti-PD-L1 therapy as part of the most recent regimen (either adjuvant monotherapy or first-line in combination with anti-CTLA-4 or VEGFR-TKI), with no more than 1 prior regimen in the metastatic setting.Read full original descriptionShow less

A Randomized, Double-Blind, Active-Control, Multicenter Phase 3 Trial of Casdatifan and Cabozantinib Versus Placebo and Cabozantinib in Patients With Advanced Clear Cell Renal Cell Carcinoma

The purpose of the study is to evaluate the progression-free survival (PFS) of casdatifan versus placebo when each is given in combination with cabozantinib for patients who received anti-PD-1 or anti-PD-L1 therapy as part of the most recent regimen (either adjuvant monotherapy or first-line in combination with anti-CTLA-4 or VEGFR-TKI), with no more than 1 prior regimen in the metastatic setting.

Inclusion: Unresectable and measurable locally advanced or metastatic renal cell carcinoma with a primary clear cell component; A Karnofsky Performance Status (KPS) score ≥ 80%; At least 1 target lesion measurable by computed tomography/magnetic resonance imaging per RECIST 1.1, not within a field of prior radiation therapy; Adequate organ and marrow function, ≤ 1 week prior to randomization; Women of childbearing potential (WOCBP) must have a negative serum pregnancy test.

Exclusion: Received prior treatment with a HIF-2α inhibitor or cabozantinib; Ongoing clinically significant toxicities related to any prior anticancer treatment, or toxicities Grade ≥ 3 per National Cancer Institute Common Terminology Criteria for Adverse Events, version 5.0 (NCI CTCAE v5.0) regardless of relatedness to prior anticancer therapies; Other prior malignancy active within the previous year except for locally curable cancers that have been apparently cured; Uncontrolled or poorly controlled hypertension, defined as a sustained blood pressure > 150 mmHg systolic or > 90 mmHg diastolic despite optimal antihypertensive treatment; History of leptomeningeal disease or spinal cord compression; NOTE: Other protocol defined Inclusion/Exclusion criteria may apply.

ClinicalTrials.gov NCT07011719 · EU CTIS 2024-515023-11-00