A Study Testing Casdatifan and Cabozantinib Compared to Placebo and Cabozantinib in Patients With Advanced Clear Cell Kidney Cancer

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What is this study about?

This study is looking at advanced clear cell renal cell carcinoma and metastatic clear cell renal cell carcinoma, which are types of kidney cancer that have spread beyond the kidney or cannot be removed by surgery. The study will use casdatifan, which is also known by its code name AB521, and cabozantinib. Some people in the study will receive casdatifan combined with cabozantinib, while others will receive placebo combined with cabozantinib. Both medications are taken by mouth as tablets.

The purpose of the study is to compare how long people live without their cancer getting worse when they take casdatifan with cabozantinib compared to when they take placebo with cabozantinib. During the study, patients will take their assigned treatment for up to 120 months. The study will check how well the treatment works by using imaging scans to see if the tumors have grown, shrunk, or stayed the same size. These scans will be reviewed by independent experts who are not directly involved in treating the patients.

The study will also look at other important outcomes, including how long people live overall, how many people see their tumors shrink, how long the tumor response lasts, and how many people have their disease stay under control for at least 16 weeks. The study team will carefully monitor any side effects that occur and will track changes in symptoms related to the kidney cancer using questionnaires that ask about disease-related symptoms. Treatment can continue for up to 10 years, and the study is expected to be completed by mid-2029.

1 Treatment assignment

You will be assigned by chance to one of two treatment groups. This process is called randomization and works like flipping a coin.

One group will receive casdatifan combined with cabozantinib.

The other group will receive placebo (an inactive substance with no medication) combined with cabozantinib.

Neither you nor your doctor will know which group you are in. This is called a double-blind study and helps ensure accurate results.

2 Daily medication intake

You will take your assigned medications by mouth in the form of tablets.

The medications should be taken according to the schedule provided by the study team.

Both cabozantinib and either casdatifan or placebo will be taken orally.

You will continue taking the study medications for as long as the treatment is beneficial and tolerable.

3 Regular imaging scans

You will undergo regular imaging tests using computed tomography or magnetic resonance imaging. These are scanning methods that create detailed pictures of the inside of your body.

These scans will measure how your cancer is responding to treatment.

The scans will be reviewed by independent experts who do not know which treatment group you are in.

4 Safety monitoring

You will have regular check-ups to monitor your health and any side effects from the medications.

Blood tests will be performed to check your organ function and blood cell counts.

Any side effects or health changes will be recorded and assessed for severity.

5 Quality of life assessments

You will be asked to complete questionnaires about your symptoms and how you are feeling.

These questionnaires focus on symptoms related to kidney cancer and how they affect your daily life.

The questionnaire used is called the National Comprehensive Cancer Network/Functional Assessment of Cancer Therapy-Kidney Symptom Index.

6 Treatment continuation

You will continue receiving the study treatment until your cancer progresses, side effects become too severe, or you decide to stop participating.

Cancer progression means the cancer has grown or spread despite treatment.

The study team will regularly evaluate whether continuing treatment is appropriate for you.

7 Follow-up period

After stopping the study treatment, you will continue to be monitored.

Information about your overall health and survival will be collected.

This follow-up period helps researchers understand the long-term effects of the treatment.

Who Can Join the Study?

  • You must have kidney cancer that cannot be removed by surgery and has spread to other parts of the body or is advanced, with a specific type called clear cell
  • You must have a Karnofsky Performance Status score of at least 80%, which means you are able to carry out normal activities and work without needing special care
  • You must have at least one tumor that can be measured using imaging tests such as CT scan (a special type of X-ray) or MRI (a scan using magnets), and this tumor must not have been treated with radiation therapy before
  • Your organs and bone marrow must be working well enough, which will be checked with blood tests done within 72 hours before joining the study
  • If you are a woman who can become pregnant, you must have a negative pregnancy test done using a blood sample

Who Cannot Join the Study?

  • The study does not list specific exclusion criteria in the provided information, which means the detailed reasons why patients cannot participate are not available in this data
  • To understand if you can participate in this study, you would need to review the complete study documentation or speak with the research team conducting the trial
  • Generally, clinical trials have exclusion criteria to ensure patient safety and that the study results are reliable, but these specific details are not included in the information provided

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name City Country Status
Institut Gustave Roussy Villejuif France
Azienda Ospedaliero Universitaria Careggi Florence Italy
Oncopole Claudius Regaud Toulouse France
Technische Universitaet Dresden Dresden Germany
Fondazione Policlinico Universitario Agostino Gemelli IRCCS Rome Italy
Medizinische Hochschule Hannover Hanover Germany
Centre Jean Perrin Clermont Ferrand France
IRCCS Humanitas Research Hospital Rozzano Italy
Azienda Ospedaliero Universitaria Consorziale Policlinico di Bari Bari Italy
Universitaetsklinikum Heidelberg AöR Heidelberg Germany
Centre Hospitalier Universitaire De Bordeaux Bordeaux France
Rostock University Medical Center Rostock Germany
University Hospital Maastricht Maastricht The Netherlands
Universitaet Leipzig Leipzig Germany
Centre Hospitalier Regional Et Universitaire De Brest Brest France

Other Sites

Site Name City Country Status
Krankenhaus Nordwest GmbH Frankfurt Germany
Istituto Oncologico Veneto Padua Italy
Ospedale Vito Fazzi Lecce Lecce Italy
Sigmedical Services S.R.L. Suceava Romania
Klinikum der Technischen Universitaet Muenchen (TUM Klinikum) Munich Germany
Netherlands Cancer Institute Amsterdam The Netherlands
Istituto Europeo Di Oncologia S.r.l. Milan Italy
IRCCS Istituto Nazionale Tumori Fondazione Pascale Naples Italy
Centro Ricerche Cliniche Di Verona S.r.l. Verona Italy
Centre Hospitalier Universitaire De Poitiers Poitiers France
Isala Klinieken Stichting Zwolle The Netherlands
Azienda Ospedaliera S Maria Di Terni Terni Italy
Hospital Universitario 12 De Octubre Madrid Spain
Masarykuv Onkologicky Ustav Brno-Stred Czechia
Fundacion Instituto Valenciano De Oncologia Valencia Spain
MD Anderson Cancer Center Madrid Spain
Europejskie Centrum Zdrowia Otwock Sp. z o.o. Otwock Poland
Ospedale Generale Provinciale Di Macerata Macerata Italy
Institut Godinot Reims France
HELIOS Klinikum Berlin-Buch GmbH Berlin Germany
Hospital Quironsalud Barcelona Barcelona Spain
Universitaetsklinikum Schleswig-Holstein AöR Kiel Germany
Centrul De Oncologie SF Nectarie S.R.L. Craiova Romania
Med Polonia Sp. z o.o. Poznan Poland
Institutul Regional De Oncologie Iasi Iasi Romania
Virgen del Rocío University Hospital Sevilla Spain
Ospedale San Raffaele S.r.l. Milan Italy
Universitair Medisch Centrum Utrecht Utrecht The Netherlands
Hospital Clinic De Barcelona Barcelona Spain
Charite Universitaetsmedizin Berlin KöR Berlin Germany
Fakultni Nemocnice Brno Brno Czechia
Fakultni Nemocnice Hradec Kralove Novy Hradec Kralove Czechia
Philipps-Universitaet Marburg Marburg Germany
Stichting Radboud University Medical Center Nijmegen The Netherlands
Fakultni Nemocnice Kralovske Vinohrady Prague Czechia
IRCCS Ospedale Policlinico San Martino Genoa Italy
Centre Hospitalier Universitaire De Montpellier Montpellier France
Fakultni Nemocnice U Sv Anny V Brne Brno-Stred Czechia
Sint Franciscus Vlietland Groep Stichting Rotterdam The Netherlands
Oncomed S.R.L. Timisoara Romania
Pratia S.A. Skorzewo Poland
Medical Center – University Of Freiburg Freiburg Im Breisgau Germany
Centrum Medyczne Medyk Sp. z o.o. Rzeszow Poland
Spitalul De Oncologie Monza S.R.L. Bucharest Romania
Hospital Alvaro Cunqueiro Vigo Spain
Institut fuer Klinische Transfusionsmedizin und Immungenetik Ulm gGmbH Ulm Germany
Hopital Beaujon Clichy France
Fondazione I.R.C.C.S. Istituto Neurologico Besta Milan Italy
Fakultni Thomayerova nemocnice Prague Czechia
Institut de Cancérologie de l’Ouest Saint-Herblain France
Provita Centrum Medyczne Sp. z o.o. Tomaszow Mazowiecki Poland
Centre Francois Baclesse Caen France
Centre De Lutte Contre Le Cancer Eugene Marquis Rennes France
Umqefyirrvbrbzfdnvnye Ezzrn Ace Essen Germany
Httgsbjd Uydgvhebscogk Mrdlgzf Dj Vlkzmucykz Santander Spain
Intzxzzb Crrqai Duaefoyedcywehtyr L'hospitalet De Llobregat Spain
Aakglpd Ski z obev Poznan Poland
Fmwsyewj nxomtmobg Mpxin a Htstxpi Prague Czechia
Abhqmihcos Piamzexq Hsyuhgvx Dh Mntvjeqeg Marseille France
Avxgiic Orxqabgopan Upmusgpkkswpt Cqtqujjwzuer Dqxve Szzoaa E Dcrqx Swuqytb Dm Ttyhir Turin Italy
Haiezbch De Lz Sfxko Cxqy I Siom Pyq Barcelona Spain
Ugqsllmqrb Donuj Sofgt Du Rhoj Li Snwyjjqp Rome Italy
Mconhmhgdmnxdfqzzowqognypj Huiswiguboznskyt Halle (Saale) Germany
Cvqshv Hgdbufwswcy Riatgzlq Dsrvvipcevtuuy Angers France
Fvkqhfxpf Paya Lc Ioycwcvtjinmc Bhgeekuth Dhz Hufytlsa Ubothuvafcjnz Ln Poi Madrid Spain
Hwappisi Vswr dwrwrend Barcelona Spain
Ifpkgttz Powhcpflpmtduet Ccaaie Cesdwc Marseille France
Cdhbdn Ojubh Lbcdahu Lille France
Hiegzuvu Urkflhqrjhlfai Sofwlltely &qnnlfs Hgpjstz dt Halevkqnwxv STRASBOURG, Alsace France

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Czechia Czechia
Recruiting
05.01.2026
France France
Recruiting
05.01.2026
Germany Germany
Recruiting
05.01.2026
Italy Italy
Recruiting
05.01.2026
Poland Poland
Recruiting
05.01.2026
Romania Romania
Recruiting
05.01.2026
Spain Spain
Recruiting
05.01.2026
The Netherlands The Netherlands
Recruiting
05.01.2026

Trial locations

Casdatifan is an investigational medication being studied in combination with cabozantinib for the treatment of advanced clear cell renal cell carcinoma, which is a type of kidney cancer. This medication is being tested to see if it can help slow down the progression of the disease when used together with cabozantinib.

Cabozantinib is a cancer medication that works by blocking certain proteins that help cancer cells grow and spread. In this trial, it is being given to all participants, either alone with a placebo or in combination with casdatifan, to treat advanced clear cell renal cell carcinoma.

Investigated diseases:

Advanced Clear Cell Renal Cell Carcinoma – This is a type of kidney cancer that has progressed beyond its early stages and involves clear cells, which appear pale or clear when examined under a microscope. Clear cell renal cell carcinoma originates in the lining of the small tubes in the kidney that filter waste from the blood and produce urine. In the advanced stage, the cancer has grown larger or spread to nearby tissues beyond the kidney. The disease may affect kidney function and cause symptoms such as blood in the urine, pain in the side, or a mass in the abdomen. As it progresses, the cancer cells continue to multiply and can interfere with normal organ function.

Metastatic Clear Cell Renal Cell Carcinoma – This is an advanced form of kidney cancer where clear cell cancer has spread from the kidney to other parts of the body. The cancer cells travel through the bloodstream or lymphatic system to form new tumors in distant organs such as the lungs, bones, liver, or brain. This represents the most progressed stage of clear cell renal cell carcinoma. The spreading process occurs when cancer cells break away from the original tumor in the kidney and establish themselves in other locations. Symptoms may vary depending on which organs are affected by the spreading cancer. The disease continues to progress as cancer cells multiply in multiple locations throughout the body.

Trial ID:
2024-515023-11-00
Protocol code:
PEAK-1
NCT ID:
NCT07011719
Trial Phase:
Therapeutic confirmatory (Phase III)

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