Study of datopotamab deruxtecan with platinum-based therapy compared to gemcitabine with platinum-based therapy in patients with advanced urothelial cancer after prior treatment

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What is this study about?

This study focuses on treating patients with Locally Advanced or Metastatic Urothelial Carcinoma, a type of cancer that affects the urinary system, including the bladder, kidney pelvis, ureter, or urethra, and has spread to nearby tissues or other parts of the body. The study will test a new medication called datopotamab deruxtecan (also known as Dato-DXd) in combination with either carboplatin or cisplatin, comparing it to a combination of gemcitabine with carboplatin or cisplatin.

The purpose of this research is to evaluate how well datopotamab deruxtecan works when combined with platinum-based therapy (carboplatin or cisplatin) compared to the standard treatment of gemcitabine with platinum-based therapy. The study is designed for patients whose cancer has progressed during or after previous treatment with enfortumab vedotin and pembrolizumab.

During the study, participants will receive their assigned treatment through intravenous infusion. The medications will be given in cycles, with treatment continuing for up to 120 weeks for datopotamab deruxtecan and up to 5 weeks for the other medications. Throughout the study, doctors will monitor the participants’ response to treatment through various medical examinations and imaging tests.

1 Initial medical assessment

You will undergo evaluation to confirm locally advanced or metastatic urothelial carcinoma (cancer in the urinary system).

Your doctor will review your medical history and perform necessary tests to ensure you meet the study requirements.

A tissue sample from your tumor will be required for testing.

2 Treatment assignment

You will be randomly assigned to receive one of two treatment combinations:

Option 1: Datopotamab deruxtecan plus either carboplatin or cisplatin

Option 2: Gemcitabine plus either carboplatin or cisplatin

All medications will be given through intravenous infusion (delivered directly into your vein)

3 Treatment period

You will receive regular treatment sessions according to your assigned medication combination

Your doctor will monitor your response to treatment through regular imaging scans

Blood tests will be performed to check your body’s response to the treatment

Your overall health status will be regularly assessed

4 Monitoring and assessment

Regular physical examinations will be conducted

Imaging scans will track any changes in your cancer

Side effects will be monitored and documented

Quality of life assessments will be performed using questionnaires

5 Follow-up period

After completing treatment, you will continue to have regular check-ups

Your health status will be monitored to track long-term outcomes

The study will continue until April 2030

Who Can Join the Study?

  • Must be 18 years or older when signing the consent form
  • Must have confirmed urothelial carcinoma (cancer in the urinary system) that is either:
    – Advanced and cannot be surgically removed, or
    – Has spread to other parts of the body (metastatic)
  • Must be able to provide a tissue sample from previous tests or agree to a new biopsy
  • Must be suitable to receive treatment with cisplatin or carboplatin (types of chemotherapy medications)
  • Must have had disease progression during or after previous treatment with enfortumab vedotin and pembrolizumab (cancer medications). Patients who stopped these treatments due to side effects are eligible if their disease has progressed
  • Must have cancer that can be measured on CT or MRI scans (imaging tests)
  • Must have good physical function, with an ECOG performance status of 0 or 1 (able to perform daily activities with minimal assistance)
  • Must have acceptable levels in laboratory tests showing:
    – Good bone marrow function
    – Good kidney function
    – Good liver function
    – Normal blood clotting

Who Cannot Join the Study?

  • History of active brain metastases (cancer that has spread to the brain) within the last 3 months
  • Known allergic reactions to platinum-based drugs or similar medications used in the study
  • Significant heart problems including heart failure or uncontrolled high blood pressure
  • Active or chronic infections, including hepatitis B, hepatitis C, or HIV
  • Other types of cancer within the past 3 years (except for successfully treated skin cancer or early-stage cancer)
  • Pregnant or breastfeeding women
  • Severe kidney or liver problems
  • Previous treatment with similar cancer medications within the past 4 weeks
  • Any medical condition that could interfere with the study treatment or affect patient safety
  • Unable to swallow medications or have conditions that could affect drug absorption
  • Participation in another clinical trial within the past 4 weeks

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name City Country Status
IRCCS Humanitas Research Hospital Rozzano Italy
Medical University Of Vienna Vienna Austria
University Hospital Jena KöR Jena Germany
Universitaetsklinikum Heidelberg AöR Heidelberg Germany
Medical University Of Graz Graz Austria
Centre Hospitalier Regional Et Universitaire De Brest Brest France
Medizinische Universitaet Innsbruck Innsbruck Austria
Institut Gustave Roussy Villejuif France
Oncopole Claudius Regaud Toulouse France
Technische Universitaet Dresden Dresden Germany
Katholieke Universiteit te Leuven Leuven Belgium
Hospital Universitario Y Politecnico La Fe Valencia Spain
CHU Grenoble Alpes La Tronche France
Centre Jean Perrin Clermont Ferrand France
Institut De Cancerologie De Lorraine Vandoeuvre Les Nancy France
Universitaetsmedizin Goettingen Goettingen Germany
Centre Hospitalier Universitaire De Bordeaux Bordeaux France

Other Sites

Site Name City Country Status
Centre Hospitalier Departemental Vendee La Roche sur Yon France
Asklepios Kliniken Hamburg GmbH Hamburg Germany
Hopitaux Universitaires Pitie Salpetriere Paris France
General University Hospital Of Larissa Larissa Greece
Universitaetsklinikum Tuebingen AöR Tuebingen Germany
Ospedale San Raffaele S.r.l. Milan Italy
Universitair Medisch Centrum Utrecht Utrecht The Netherlands
Alexandra Hospital Athens Greece
Hospital Clinic De Barcelona Barcelona Spain
Stichting Radboud University Medical Center Nijmegen The Netherlands
IRCCS Ospedale Policlinico San Martino Genoa Italy
Aalborg University Hospital Aalborg Denmark
General University Hospital Of Patras Patras Greece
Region Midtjylland Aarhus Denmark
Rigshospitalet Copenhagen Denmark
Centre Hospitalier Universitaire De Nimes Nimes France
IRCCS Istituto Nazionale Tumori Fondazione Pascale Naples Italy
Centre hospitalier universitaire de Liege Liege Belgium
Institut fuer Klinische Transfusionsmedizin und Immungenetik Ulm gGmbH Ulm Germany
Universitair Ziekenhuis Gent Gent Belgium
Universitaetsklinikum Aachen AöR Aachen Germany
Universitaetsklinikum Schleswig-Holstein AöR Kiel Germany
Centre Hospitalier Lyon Sud Pierre Benite France
Hospital General Universitario Gregorio Maranon Madrid Spain
Hopital Beaujon Clichy France
Hospital Universitario 12 De Octubre Madrid Spain
Hospital Del Mar Barcelona Spain
Helse Stavanger HF Stavanger Norway
Universita Degli Studi Di Brescia Brescia Italy
Az Maria Middelares Gent Gent Belgium
Stadt Wien Wiener Gesundheitsverbund Vienna Austria
Universitaetsklinikum Krems Krems An Der Donau Austria
Fondazione I.R.C.C.S. Istituto Neurologico Besta Milan Italy
Clinique Victor Hugo Le Mans France
Capio La Croix Du Sud Quint-Fonsegrives France
General Hospital Of Thessaloniki Papageorgiou Thessaloniki Greece
Polyclinique De Blois La Chaussee St Victor France
Clinique de l’Europe Amiens France
Centre Francois Baclesse Caen France
L’Hopital Prive Du Confluent Nantes France
Sykehuset I Vestfold HF Tonsberg Norway
Azienda Ospedaliero-Universitaria San Luigi Gonzaga Orbassano Italy
Klinikum Der Landeshauptstadt Stuttgart gKAöR Stuttgart Germany
Istituto Di Candiolo Fondazione Del Piemonte Per Loncologia IRCCS Candiolo Italy
Hospital Universitario Quironsalud Madrid Pozuelo De Alarcon Spain
Universita’ Di Pisa Pisa Italy
Hospital Universitario Virgen De Valme Sevilla Spain
Cliniche Gavazzeni S.p.A. Bergamo Italy
St. Elisabeth Gruppe GmbH Katholische Kliniken Rhein-Ruhr Herne Germany
Staedtisches Klinikum Dresden Dresden Germany
Centro Ricerche Cliniche Di Verona S.r.l. Verona Italy
Centre Hospitalier Universitaire De Poitiers Poitiers France
Azienda Ospedaliera S Maria Di Terni Terni Italy
Næstved Hospital Næstved Denmark
Saint Savvas Oncology Hospital Athens Greece
Studienpraxis Urologie Susan Feyerabend MD Tilman Todenhoefer MD PhD GbR Nuertingen Germany
Centre De Cancerologue Du Grand Montpellier Montpellier France
SCRI CCCIT Ges.m.b.H. Salzburg Austria
Hospital Quironsalud Barcelona Barcelona Spain
MD Anderson Cancer Center Madrid Spain
Azienda Sanitaria Locale Napoli 2 Nord Frattamaggiore Italy
Azienda Socio Sanitaria Territoriale Ovest Milanese Legnano Italy
Institut Godinot Reims France
Krankenhaus Der Barmherzigen Brueder Wien Vienna Austria
Institut de Cancérologie de l’Ouest Saint-Herblain France
Metropolitan Hospital Athens Greece
Imardarb Pcrpoubljaholxi Czflad Calmvl Marseille France
Uqdxhmoyga Hmweakgk Carikho Cologne Germany
Frfsmgwo nchsrwewv Mndpk a Hbqubpx Prague Czechia
Ahhpzwnxwp Pjhqiwwi Hbjkutom Dz Mfncmhpqd Marseille France
Agmtlqag Ufqycbgicj Hcpufxhi Lorenskog Norway
Exjatlc Ufdoqapvkdwl Mbwnpwt Cmpuodb Rgvqedipo (orpnvyj Mda Rotterdam The Netherlands
Atehhq Mxudndd Cblwun Spgz Thessaloniki Greece
Kxquvqfh dfa Upffsbnadbrl Muqhkloi Avx Munich Germany
Hloaeeeb Du Lz Stpno Crvf I Sszu Pln Barcelona Spain
Chgiez Lfyd Bucpud Lyon France
Uidyekspjn Og Auskovg Edegem Belgium
Ucpxtlsnwncwtgfmznhwq Ewgpr Ayq Essen Germany
Ilrmjh Iinstyrn Fnvyicsnnxwdp Oihnhceahnc Rome Italy
Ojrmcdleretuch Lzai Gohh Linz Austria
Iebnkfex Czudfl Dbxqbhrtcyhjxhfbf L'hospitalet De Llobregat Spain
Feqmkferc Pizz Ld Ihjxqcjkxhfqz Brmjrgcvq Dqy Haptuvvf Urtxyfusqmldv Lj Pgb Madrid Spain
Ueonqfikhc Gfaqdct Hqebmqhi Aninacf Athens Greece
Htcenejr Uzecowpmomcwei Sgjjhmbwjj &kzoasx Hmxbvsb dp Hyybqwmskkx STRASBOURG, Alsace France
Iuabysxj Risiercq Dd Cynbks Dk Mppqvkjbjdr Montpellier France
Tjzjrfeitt Ceibci Htbcahbo Thessaloniki Greece
Fdqormtomrmhag fyn Uaryfudn Dtn Ejuppj Eisleben Germany
Cbgojz Hdwgjdowmme Dx Jfyv Ejmy Tppdna Calais France
Iaeoagez df Ccgvhanowplb Hernfmxaxcr Urppfzmsomwpg dm Soqgx Enesovl (wtfmksd Saint Priest En Jarez France
Mkgfpiycptclreptmwkxpvzjne Hrzcyfhfkatabmjc Halle (Saale) Germany
Hovvzvjj Uivddiumrqfjb Dm Bcbbehi Badajoz Spain

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

Trial status

Country Status Recruitment Start
Austria Austria
Recruiting
10.12.2025
Belgium Belgium
Not yet recruiting
10.12.2025
Czechia Czechia
Not yet recruiting
10.12.2025
Denmark Denmark
Not yet recruiting
10.12.2025
France France
Recruiting
10.12.2025
Germany Germany
Recruiting
10.12.2025
Greece Greece
Not yet recruiting
10.12.2025
Italy Italy
Not yet recruiting
10.12.2025
Norway Norway
Not yet recruiting
10.12.2025
Spain Spain
Not yet recruiting
10.12.2025
The Netherlands The Netherlands
Not yet recruiting
10.12.2025

Trial locations

Datopotamab Deruxtecan (also known as Dato-DXd) is an antibody-drug conjugate medication that targets specific cancer cells in patients with urothelial carcinoma (bladder cancer and cancers of the urinary system). It works by delivering cancer-fighting medicine directly to tumor cells.

Carboplatin is a chemotherapy medication used to treat various types of cancer. It works by interfering with cancer cell DNA, which helps stop cancer cells from growing and dividing.

Cisplatin is a chemotherapy medication similar to carboplatin. It also works by damaging cancer cell DNA to stop tumor growth and spread.

Gemcitabine is a chemotherapy medication that works by preventing cancer cells from making and repairing DNA, which stops them from multiplying.

Enfortumab Vedotin is an antibody-drug conjugate that targets specific proteins found on cancer cells to deliver cancer-fighting medicine directly to the tumors.

Pembrolizumab is an immunotherapy medication that helps the body’s immune system recognize and fight cancer cells more effectively.

Investigated Diseases:

Urothelial Carcinoma – A type of cancer that begins in the cells lining the urinary system, most commonly in the bladder. The disease can develop in the renal pelvis, ureter, bladder, and urethra, affecting the transitional epithelial cells that make up the inner lining of these organs. When described as locally advanced, the cancer has grown into deeper layers of the bladder wall or nearby tissues. In metastatic form, the cancer has spread beyond its original location to other parts of the body, such as lymph nodes, bones, liver, or lungs. The condition typically develops gradually, with the abnormal cells multiplying and forming tumors in the urinary system.

Trial ID:
2024-516906-47-00
Protocol code:
DS1062-328
Trial Phase:
Therapeutic use (Phase IV)

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