Study of BT8009 Alone or with Pembrolizumab for Patients with Advanced or Metastatic Bladder Cancer

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What is this study about?

This clinical trial is focused on studying treatments for urothelial cancer, which is a type of cancer that affects the bladder and other parts of the urinary system. The study will explore the effectiveness of a new treatment called BT8009, both on its own and in combination with other medications. These medications include pembrolizumab, cisplatin, carboplatin, gemcitabine, and avelumab. The purpose of the study is to see how well these treatments work in slowing down the progression of the cancer or in reducing the size of the tumors.

Participants in the study will be divided into different groups. Some will receive BT8009 alone, while others will receive it in combination with pembrolizumab. Another group will receive a combination of chemotherapy drugs, which may include cisplatin or carboplatin with gemcitabine, and possibly avelumab as a maintenance treatment. The study will monitor the participants over a period of time to assess the effectiveness of these treatments in managing the cancer.

The trial aims to provide valuable information on how these treatments can help patients with advanced stages of urothelial cancer. By comparing the different treatment options, researchers hope to find the most effective approach to improve the outcomes for patients with this type of cancer. Participants will receive regular assessments to track the progress of their treatment and any changes in their condition.

1 joining the study

Upon joining the study, participants are assigned to one of two groups, known as cohorts. Each cohort has a different treatment plan.

2 treatment for cohort 1

Participants in Cohort 1 receive a combination of medications. This includes BT8009 and pembrolizumab, or chemotherapy with cisplatin or carboplatin and gemcitabine. If indicated, avelumab is used for maintenance.

All medications are administered as a solution for infusion, which means they are given through a vein. The specific dosage and frequency depend on the treatment plan and medical guidance.

3 treatment for cohort 2

Participants in Cohort 2 receive BT8009 as a single treatment or in combination with pembrolizumab. These medications are also administered as a solution for infusion.

The dosage and frequency are determined by the treatment plan and medical guidance.

4 monitoring and evaluation

Throughout the study, participants undergo regular monitoring to assess the effectiveness of the treatment. This includes measuring progression-free survival and overall response rate using specific criteria.

Evaluations are conducted by an independent review to ensure accuracy and objectivity.

5 end of treatment

The study continues until the estimated end date of December 31, 2030, or until specific endpoints are reached, such as disease progression or other criteria defined in the study.

Participants are informed about the results and any further steps after the study concludes.

Who Can Join the Study?

  • Must be able to understand the study procedures and agree to participate by providing written consent.
  • Must be at least 18 years old.
  • Must have a confirmed diagnosis of locally advanced (cannot be removed by surgery) or metastatic (cancer has spread to other parts of the body) urothelial cancer of the kidney area, ureter, bladder, or urethra. If the cancer has mixed types, the main type should be transitional cell (at least 50%).
  • Must have measurable disease, meaning the cancer can be measured using specific criteria. If the cancer was treated with radiation before, it should show signs of growth to be considered measurable.
  • Must have available tumor tissue from a previous or new sample for testing in a central lab.
  • Must have a life expectancy of at least 12 weeks.
  • Must have adequate organ function, which includes:
    • Total bilirubin (a substance made by the liver) should be within normal limits, or slightly higher if the person has Gilbert disease (a mild liver disorder).
    • Serum albumin (a protein in the blood) should be at least 2.5 g/dL.
    • Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) (liver enzymes) should be within normal limits, or slightly higher if there are liver metastases (cancer spread to the liver).
    • Alkaline phosphatase (an enzyme related to the liver and bones) should be within normal limits, or slightly higher if there are liver or bone metastases.
    • Estimated glomerular filtration rate (eGFR) (a measure of kidney function) should be at least 30 mL/min.
  • International normalized ratio (INR)/prothrombin time (PT) (measures of blood clotting) should be within normal limits unless taking blood thinners, in which case they should be within the therapeutic range.
  • Women who can have children must have a negative pregnancy test before starting the study.
  • Women and men must agree to use highly effective birth control methods during the study and for a specific time after the last dose of study drugs. Men must also agree not to donate sperm, and women must not breastfeed or donate eggs during this time.

Who Cannot Join the Study?

  • Patients who have a different type of cancer than locally advanced or metastatic urothelial cancer cannot participate. This type of cancer affects the bladder and nearby areas.
  • Patients who are not within the specified age range for the study cannot participate. The study is open to certain age groups only.
  • Patients who are not able to follow the study procedures or take the study medications as required cannot participate.
  • Patients who have other serious health conditions that might interfere with the study cannot participate.
  • Patients who are pregnant or breastfeeding cannot participate, as the study may affect the baby.
  • Patients who have participated in another clinical trial recently may not be eligible to participate.
  • Patients who have allergies or reactions to the study medications cannot participate.
  • Patients who have not recovered from previous treatments or surgeries may not be eligible to participate.

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
Technische Universitaet Dresden Dresden Germany
Oslo Universitetssykehus HF Oslo Norway
Medical University Of Vienna Vienna Austria
Universitaetsmedizin Goettingen Goettingen Germany
Universitaetsklinikum Heidelberg AöR Heidelberg Germany
Centre Hospitalier Universitaire De Bordeaux Bordeaux France
Uniwersytecki Szpital Kliniczny Im Jana Mikulicza Radeckiego We Wroclawiu Wroclaw Poland
Katholieke Universiteit te Leuven Leuven Belgium
Hospital Universitario De Navarra Pamplona Spain

Other Sites

Site Name City Country Status
Krankenhaus Nordwest GmbH Frankfurt Germany
Istituto Oncologico Veneto Padua Italy
Pauls Stradins Clinical University Hospital Riga Latvia
University Multiprofile Hospital For Active Treatment Sofiamed OOD Sofia Bulgaria
Centre Antoine Lacassagne Nice France
Azienda Ospedaliero-Universitaria Policlinico G. Rodolico-San Marco Di Catania Catania Italy
Mater Misericordiae University Hospital Dublin Ireland
Orszagos Onkologiai Intezet Budapest Hungary
Centrum Onkologii Im. Prof. Franciszka Lukaszczyka W Bydgoszczy Bydgoszcz Poland
Centro Di Riferimento Oncologico Di Aviano Aviano Italy
Azienda Socio Sanitaria Territoriale Di Cremona Cremona Italy
Istituto Europeo Di Oncologia S.r.l. Milan Italy
IRCCS Istituto Nazionale Tumori Fondazione Pascale Naples Italy
Centre Hospitalier Universitaire De Poitiers Poitiers France
Azienda Ospedaliero Universitaria Di Modena Modena Italy
Universitair Ziekenhuis Gent Gent Belgium
Azienda Ospedaliera S Maria Di Terni Terni Italy
Hospital General Universitario Gregorio Maranon Madrid Spain
Næstved Hospital Næstved Denmark
Hospital Universitario 12 De Octubre Madrid Spain
Masarykuv Onkologicky Ustav Brno-Stred Czechia
Unidade Local De Saude De Gaia/Espinho E.P.E. Vila Nova De Gaia Portugal
Az Maria Middelares Gent Gent Belgium
Centrum Onkologii Ziemi Lubelskiej Im. Sw. Jana Z Dukli Lublin Poland
Fundacion Instituto Valenciano De Oncologia Valencia Spain
Instituto Portugues De Oncologia Do Porto Francisco Gentil E.P.E. Porto Portugal
Grand Hopital De Charleroi Charleroi Belgium
Studienpraxis Urologie Susan Feyerabend MD Tilman Todenhoefer MD PhD GbR Nuertingen Germany
Daugavpils regionala slimnica SIA Daugavpils Latvia
Complex Oncological Center Plovdiv EOOD Plovdiv Bulgaria
Copernicus Podmiot Leczniczy Sp. z o.o. Gdansk Poland
Complejo Hospitalario Universitario Insular Materno Infantil Las Palmas De Gran Canaria Spain
Unidade Local De Saude De Matosinhos E.P.E. Senhora Da Hora Portugal
Mazowiecki Szpital Onkologiczny Sp. z o.o. Wieliszew Poland
Krankenhaus Der Barmherzigen Brueder Wien Vienna Austria
Tallaght University Hospital Dublin Ireland
General University Hospital Of Larissa Larissa Greece
Centrul De Oncologie SF Nectarie S.R.L. Craiova Romania
Centre Hospitalier Intercommunal De Cornouaille Quimper France
Somogy Varmegyei Kaposi Mor Oktato Korhaz Kaposvar Hungary
Sørlandet sykehus Kristiansand Kristiansand Norway
Scm Sp. z o.o. Cracow Poland
Universitaetsklinikum Tuebingen AöR Tuebingen Germany
Ospedale San Raffaele S.r.l. Milan Italy
Azienda Ospedaliero-Universitaria San Luigi Gonzaga Orbassano 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
Champalimaud Clinical Centre Lisbon Portugal
University Hospital Galway Galway Ireland
Hospital Universitario Fundacion Jimenez Diaz Madrid Spain
IRCCS Ospedale Policlinico San Martino Genoa Italy
Universita’ Di Pisa Pisa Italy
Universita’ Politecnica Delle Marche Ancona Italy
Universidade De Santiago De Compostela Santiago De Compostela Spain
Aalborg University Hospital Aalborg Denmark
Uniteversity Muliprofile Hospital For Active Treatment Tsaritsa Yoanna-Isul EAD Sofia Bulgaria
Oncomed S.R.L. Timisoara Romania
Zala Megyei Szent Rafael Korhaz Zalaegerszeg Hungary
Medical Center – University Of Freiburg Freiburg Im Breisgau Germany
Liepajas Regionala Slimnica SIA Liepaja Latvia
University Hospital Olomouc Olomouc Czechia
St. Elisabeth Gruppe GmbH Katholische Kliniken Rhein-Ruhr Herne Germany
Spitalul De Oncologie Monza S.R.L. Bucharest Romania
Centre Hospitalier Lyon Sud Pierre Benite France
Hopital Beaujon Clichy France
Universita Degli Studi Di Brescia Brescia Italy
Institut Sainte Catherine Avignon France
Immobiliere De Nancy Nancy France
Fondazione I.R.C.C.S. Istituto Neurologico Besta Milan Italy
Clinique Victor Hugo Le Mans France
Budapesti Uzsoki Utcai Korhaz Budapest Hungary
Sykehuset I Vestfold HF Tonsberg Norway
Iwbaibnf Rdksljtw Df Cijjtg Dy Mkpuxmuxzex Montpellier France
Ubngptlphpxjqgtmembns Etlgg Alv Essen Germany
Orfdilxmavtlej Lbal Glum Linz Austria
Hgmmvyfv Uyrbqyooemrmn Mjrljae Dg Vbyioreejt Santander Spain
Cgya Uxnnebkjgv Hetvcixs Cork Ireland
Iepgbziw Cslqrp Dtxvlccjmlggqihjv L'hospitalet De Llobregat Spain
Sgovqdpi Pawbegnrn Sod z otkk Gdynia Poland
Ibobqchm Mcaxnptbum Mdhqruarje Paris France
Lomlvfvs Sgmz Lisbon Portugal
Bcrvcvnaatg Vijeodqsl Oefgnxhhbpnk Kecskemet Hungary
Iumnkvkk Buioosmr Bordeaux France
Ftbugdro ntwwvletu Msaxr a Hifajam Prague Czechia
Cnzhru Hajcezuwuks Eo Uuuzqbnqcxxdq Dt Lmtattn Limoges France
Ipinzmhs Rhyxyupdf Phh Lb Stselg Daq Tdncnn Dikx Alqxsun Iyec Sqrpzh Meldola Italy
Azbavebpe Upu Amsterdam The Netherlands
Acxfdgwh Ubxjeiodtq Hlchgloc Lorenskog Norway
Brbebxjg Ugfzlscsac Hyuaanlc Cyrcdb Besançon France
Eebuevh Upfidbccujne Mcxwdwx Cbyfrio Rynzbaaap (vsnxjoa Mdj Rotterdam The Netherlands
Udlalsnmmjbhunvpuamdv Mmzofehd Acw Munster Germany
Htxzxzkh Uiaczqxpgmvti Dwvclzca Donostia / San Sebastian Spain
Atndrg Mmbhbbl Ctntuz Sykk Thessaloniki Greece
Nitrwqex Ixbqxdtq Ohifgubro Iqv Mcobp Szlbesxrmxsebfgznxomruswjfwq Ifuelnqa Bnfbgitm Cracow Poland
Gdpyso Udfruatcnu Fdoejfmbf Frankfurt Germany
Addkydv Uudia Szbbrbwkn Laznnc Dl Buxcgyi Bologna Italy
Hlqdslga De Lu Swffm Ctjo I Sdvn Pyn Barcelona Spain
Sh Vpepkdihybtxqou Ueqecflxke Hyykvaxt Dublin Ireland
Cslwon Lupq Bxvkjs Lyon France
Farfurych Pzcn Lg Ihktxkagvutti Belicpcxd Dko Hhtcrkdv Usgiwmcxnhank Lu Ptl Madrid Spain
Irlvmpoz Phdhycmvjsmdnac Cwaqhy Crkgwu Marseille France
Upgfyyidys Gpdmdsi Hqhtbeqa Aaziuon Athens Greece

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

Trial status

Country Status Recruitment Start
Austria Austria
Not recruiting
15.09.2024
Belgium Belgium
Not recruiting
15.09.2024
Bulgaria Bulgaria
Not recruiting
15.09.2024
Czechia Czechia
Not recruiting
15.09.2024
Denmark Denmark
Not recruiting
15.09.2024
France France
Not recruiting
15.09.2024
Germany Germany
Not recruiting
15.09.2024
Greece Greece
Not recruiting
15.09.2024
Hungary Hungary
Not recruiting
15.09.2024
Ireland Ireland
Not recruiting
15.09.2024
Italy Italy
Not recruiting
15.09.2024
Latvia Latvia
Not recruiting
15.09.2024
Norway Norway
Not recruiting
15.09.2024
Poland Poland
Not recruiting
15.09.2024
Portugal Portugal
Not recruiting
15.09.2024
Romania Romania
Not recruiting
15.09.2024
Spain Spain
Not recruiting
15.09.2024
The Netherlands The Netherlands
Not recruiting
15.09.2024

Trial locations

BT8009 is an investigational medication being studied for its potential to treat urothelial cancer. It is being tested both as a standalone treatment and in combination with another medication to see how well it works in stopping or slowing the growth of cancer.

Pembrolizumab is a medication that helps the immune system fight cancer. It is used in combination with BT8009 in this study to see if it can improve the effectiveness of the treatment for urothelial cancer.

Cisplatin is a chemotherapy drug used to treat various types of cancer, including urothelial cancer. It works by damaging the DNA of cancer cells, which can stop them from growing and dividing.

Carboplatin is another chemotherapy medication similar to cisplatin. It is used to treat cancer by interfering with the DNA of cancer cells, preventing them from multiplying.

Gemcitabine is a chemotherapy drug that is often used in combination with other medications to treat cancer. It works by blocking the ability of cancer cells to make DNA, which is necessary for them to grow and divide.

Avelumab is a medication that helps the immune system attack cancer cells. It is used as a maintenance therapy in this study, which means it is given after initial treatment to help keep the cancer from coming back or getting worse.

Investigated diseases:

Locally advanced or metastatic urothelial cancer – This is a type of cancer that begins in the urothelial cells lining the bladder, ureters, or other parts of the urinary tract. When it is locally advanced, the cancer has spread beyond the original site but is still within the nearby tissues. In the metastatic stage, the cancer has spread to distant parts of the body, such as the lymph nodes, bones, or lungs. The disease progresses as cancer cells grow and invade surrounding tissues, potentially leading to symptoms like blood in the urine, pain, or difficulty urinating. As it advances, it may cause more systemic symptoms due to its spread to other organs. The progression can vary greatly among individuals, depending on factors like the cancer’s location and the patient’s overall health.

Trial ID:
2023-504231-41-01
Protocol code:
BT8009-230
NCT ID:
NCT06225596
Trial Phase:
Therapeutic use (Phase IV)

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