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
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
Comite Entreprise Paul Papin Angers France

Other Sites

Site Name City Country Status
Ospedale San Raffaele S.r.l. Milan Italy
IRCCS Istituto Nazionale Tumori Fondazione Pascale Naples Italy
Hospital General Universitario Gregorio Maranon Madrid Spain
Hopital Beaujon Clichy France
Hospital Del Mar Barcelona Spain
Az Maria Middelares Gent Gent Belgium
Universitaetsklinikum Krems Krems An Der Donau Austria
Capio La Croix Du Sud Quint-Fonsegrives France
Centre Francois Baclesse Caen France
L’Hopital Prive Du Confluent Nantes France
Centre De Cancerologue Du Grand Montpellier Montpellier France
Azienda Sanitaria Locale Napoli 2 Nord Frattamaggiore Italy
Metropolitan Hospital Athens Greece
University Hospital Olomouc Olomouc Czechia
Cnekjs Hwwycrokbvs Doahxkxxwphuf Vjamqi La Roche sur Yon France
Awmqwfvvb Kltviopo Hqabxea Geno Hamburg Germany
Hnyvyfud Uhfdtotiatcegh Puqhg Slzbedmmapb Paris France
Gdoxyhm Uhzhfmhrbm Hqztqhez Oo Lnyshzi Larissa Greece
Icytglir Pntzqkwwpknhpck Crjcyq Ctydcc Marseille France
Uycwqrptvw Hfeouygs Cdtehof Cologne Germany
Foxwkfmh nvnzcloxw Mbvpp a Hruyhlf Prague Czechia
Ukmjkusplzeltlodnjepf Tymscerrt Acv Tuebingen Germany
Adrhqraalv Pxjspetf Hqbptwsk Dy Mlnmcwbbr Marseille France
Uhtoionhkqai Mxcunlh Cfwbmcs Uaakrpd Utrecht The Netherlands
Atmvcdbgp Hwokkqof Athens Greece
Awivejen Uupdhlbhbb Hokdootl Lorenskog Norway
Htwiajzt Cempdf Dl Bvpqxxfjp Barcelona Spain
Ebjfbia Udeiuaagkmyh Mrfioyf Cbowzzk Rhtihglgl (nhuueyy Mpi Rotterdam The Netherlands
Sficudmnf Rbtneru Uczwlvjiei Meavgny Copnjk Nijmegen The Netherlands
Ipaye Ojhbjxrn Pylyevfmvpt Sru Mcnboin Genoa Italy
Abfhryo Ujxpllbvbp Hbyugyxp Aalborg Denmark
Guoiuhy Uweivwjjlw Hktdixhl Ou Phkyin Patras Greece
Uhvcqqcitmvikcnvqqzkn Hqifiejzxw Avk Heidelberg Germany
Arcotc Mbgxdgn Cgcuhw Sflb Thessaloniki Greece
Kmtuswrh dav Uwewgzrwqmkj Mxjjelys Ala Munich Germany
Rfdnmw Musbhmfyycy Aarhus Denmark
Rjuiunscrvbmcs Copenhagen Denmark
Hszwborx Df Li Sdyys Cmjx I Soov Psb Barcelona Spain
Cgiiil Lopv Bjvgqs Lyon France
Umusvjjnsk Ot Azwjunw Edegem Belgium
Csiymu Hkwxmxefjel Ufiycbpdvtdqx Dt Ngaxl Nimes France
Uunhivxgfrzxwdizkcrxg Exakl Ayd Essen Germany
Ihbxeh Ijlqmuko Fqwoxkvkjrkrn Odqfcmwyxhx Rome Italy
Oablcprzsxjrmj Ldfk Gfds Linz Austria
Camily hlcoxcqzwjh utczraxuzdxnu dt Lvjla Liege Belgium
Irtpoege fjhy Kaiwjrfyf Tzwusemoycewikdetsn usr Irrzjywjcfgp Uup gwctn Ulm Germany
Uofbaosplmtg Zlyifssbzl Gnkx Gent Belgium
Uxvzjylseljrnieoiqaml Aiztrx Alv Aachen Germany
Udrptmyfxlduzwchdvfmj Slhzfwtdpgtkxmzahf Awc Kiel Germany
Csench Himlqslnsyw Lfvb Sta Pierre Benite France
Hxlzjbnv Upngzkzehcipg 1w Dl Ootcruk Madrid Spain
Hdvkz Swponpcpz Hk Stavanger Norway
Iswevdva Chazlb Dgksjxvyhfvklsbgd L'hospitalet De Llobregat Spain
Ujvnkyueai Dqnro Sjowq Db Beoyujq Brescia Italy
Fumveywxy Pkpq Lm Imfuhnhxpcdqm Bujolizen Dxg Hzzgnfzb Uzvnaogzuhlvo Lk Plv Madrid Spain
Skbks Wesc Wckcyw Gwstgisthbjlmqlnnw Vienna Austria
Ffolmlczdg Ilqaosnhfh Iudrcwvq Ncjzfcalaud Bljrm Milan Italy
Hknxvlfi Unicjyitrytign Slxbtekqqy &frxnuz Hgnmmny dw Hmqwgockmea STRASBOURG, Alsace France
Iuntlydi Rnvzaekk Dc Chelpy Dv Mzmrbemfqna Montpellier France
Tijtfcbwya Cnwcol Hdxmbgli Thessaloniki Greece
Cgijawxr Vttyof Hgoh Le Mans France
Fmbjjkpekovkhi fnx Uhhekbmf Dgg Euophf Eisleben Germany
Gfjhfzf Huizqcpi On Tkyunfqfzswe Pifshvkfqvsi Thessaloniki Greece
Pxsoybepqhdl Dn Bsxri La Chaussee St Victor France
Cmnwnh Htligjnstsk Du Jfkz Emvp Tnehig Calais France
Ifiejuur dv Cdubridmlmzf Hijbkrhywcn Urcsraxuemeyh dn Sdguj Eteapsa (uxnwprr Saint Priest En Jarez France
Cmqtsmhn dr ltocprgpxwhybf Amiens France
Sbcjeyvjn I Vazlqlit Hw Tonsberg Norway
Aopxxeb Omlcvpcytyleouslfzncwwmtk Swz Lbuxs Gxveysl Orbassano Italy
Kledplrd Dyp Lmkxqudmaeizggnl Shsstnhqj gvzdn Stuttgart Germany
Ibqjrwuv De Crakbnga Fgwsmxqclq Dab Pztpasjf Plo Lmssytkbxa Idjzc Candiolo Italy
Hciyjnwp Unmglsksexywh Qyksrbyibiu Mgxzif Pozuelo De Alarcon Spain
Hurncpxr Ujnpdascokrug Vgvcyv Dl Vklfu Sevilla Spain
Cnykfaht Gbgsxkkgg Srzzmz Bergamo Italy
Srk Eqkwinnuf Gykygy Gwsz Klqhgxjgkbl Kpttgdtq Rkxwfuvbuz Herne Germany
Skcuvkukrwez Kzolwviy Defmkmf Dresden Germany
Csieiu Rtjxgajn Cphihdyx Ds Vziyvo Ssndsp Verona Italy
Cxmrmi Hrllbqfzlkq Uqhtbmmtipzvm Dv Pvjloemd Poitiers France
Amtssoq Oiypdywnisx S Mflba Da Thocc Terni Italy
Mqmcrldctuyuufuhtvgkrltwxg Hkfcnfheusxbrirc Halle (Saale) Germany
Ndhjcfd Hlocohzz Næstved Denmark
Swxfo Sqvnln Osftsisg Hhwnkodu Athens Greece
Hpzirtgt Uaypaomnclldm De Bfxebih Badajoz Spain
Sbesyjmmslxzi Ufabenly Sgunb Fhatxnqwsd Mo Twawre Tnvkupnbnfm Mx Pti Gac Nuertingen Germany
Swsd Cnnty Glecqlazir Salzburg Austria
Htbomvda Qjirewrcuih Bwmvnrxsl Barcelona Spain
Mt Aeeiwzod Cfegha Cuxviq Madrid Spain
Acggbjm Sznpv Sdcjpqzod Taajwubjxmal Olegr Maetoask Legnano Italy
Iesttdjl Gthrfdf Reims France
Ksxhxbsmfkd Dsk Bkksgrlsglrn Bykmxgt Wnlz Vienna Austria
Hiunat Hstsashq Herlev Denmark
Urpujpgdbp Gugmzpg Htpfsclc Aqcsoaj Gyjyzjc Hkmlcqhn Oj Wctj Awsmwf H Aooo Vtfjshr Chaidari Greece
Abawidc Opkawkcikjv Uxxrtrjaclcve Pbisjc Pisa Italy
Ujmwwjosnw Hodpdeex Meodahodzi Maastricht The Netherlands
Ahjdlrrjr Uazr lnucejo Agz Amsterdam The Netherlands
Vvbjrskdq Fsfuptgg Nmoezukuc V Pksbv Prague Czechia

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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