Condition: Metastatic Clear Cell Renal Cell Carcinoma · Advanced Clear Cell Renal Cell Carcinoma · Sponsor: Arcus Biosciences, Inc.
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.
This description comes directly from the study's public registry record.
Medical Director · +1-510-462-3330 · clinicaltrials@arcusbio.com
Always discuss trial participation with your own doctor first.
| Research Site | Gilbert, Arizona, United States | Recruiting |
| Research Site | Goodyear, Arizona, United States | Recruiting |
| Research Site | Phoenix, Arizona, United States | Recruiting |
| Research Site | Duarte, California, United States | Recruiting |
| Research Site | La Jolla, California, United States | Recruiting |
| Research Site | Los Angeles, California, United States | Recruiting |
| Research Site | Sacramento, California, United States | Recruiting |
| Research Site | San Diego, California, United States | Recruiting |
| Research Site | New Haven, Connecticut, United States | Recruiting |
| Research Site | Washington D.C., District of Columbia, United States | Recruiting |
| Research Site | Jacksonville, Florida, United States | Recruiting |
| Research Site | Miami, Florida, United States | Recruiting |
+ 122 more locations — full list on the registry record.
Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.
We email about this public record only. Unsubscribe anytime with one click. Never medical advice.
This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT07011719