Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at UCSD
Dates
study started
study ends around

Description

Summary

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 in adult patients with confirmed advanced or metastatic clear cell Renal Cell Carcinoma who have experienced progression on or after prior anti-PD-1 or anti-PD-L1 immunotherapy.

Official Title

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

Keywords

Metastatic Clear Cell Renal Cell Carcinoma, Advanced Clear Cell Renal Cell Carcinoma, Casdatifan, Kidney Cancer, PEAK-1, AB521, ccRCC, Clear-cell metastatic renal cell carcinoma, Kidney Neoplasms, cabozantinib

Eligibility

You can join if…

Open to people ages 18 years and up

  • 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, ≤ 72 hours prior to randomization.
  • Women of childbearing potential (WOCBP) must have a negative serum pregnancy test.

You CAN'T join if...

  • Received prior treatment with a HIF-2α inhibitor or cabozantinib.
  • Other prior malignancy active within the previous year except for locally curable cancers that have been apparently cured.
  • 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.
  • Uncontrolled or poorly controlled hypertension, as defined by a sustained blood pressure > 140/90 mm Hg on more than three antihypertensives
  • History of leptomeningeal disease or spinal cord compression.

NOTE: Other protocol defined Inclusion/Exclusion criteria may apply.

Locations

  • University of California San Diego Moores Cancer Center accepting new patients
    La Jolla 5363943 California 5332921 92037 United States
  • University of California San Diego Moores Cancer Center accepting new patients
    San Diego 5391811 California 5332921 92103 United States
  • City Of Hope National Medical Center accepting new patients
    Duarte 5344147 California 5332921 91010 United States

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Arcus Biosciences, Inc.
ID
NCT07011719
Phase
Phase 3 research study
Study Type
Interventional
Participants
Expecting 720 study participants
Last Updated