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A Study of TAR-200 in Combination With Cetrelimab and Cetrelimab Alone in Participants With Muscle-Invasive Urothelial Carcinoma of the Bladder

Phase 2
Active, not recruiting
Conditions
Urinary Bladder Neoplasms
Interventions
Registration Number
NCT04919512
Lead Sponsor
Janssen Research & Development, LLC
Brief Summary

The purpose of this study is to evaluate the anti-tumor effects of TAR-200 in combination with intravenous (IV) cetrelimab and IV cetrelimab alone.

Detailed Description

Bladder cancer is the tenth most common malignancy worldwide. Approximately 25 percent (%) of all new bladder cancer participants present with muscle invasive bladder cancer (MIBC) at the time of diagnosis, and roughly 50% will ultimately develop distant metastases. The TAR-200/ gemcitabine (JNJ-17000139) product is an intravesical drug delivery system regulated as an investigational drug. The drug constituent consists of gemcitabine minitablets and osmotic minitablets. Cetrelimab (JNJ-63723283) is a fully human immunoglobulin G4 (IgG4) kappa monoclonal antibody (mAb) that binds programmed-cell death protein (PD)-1. The standard of care in MIBC includes radical cystectomy (RC) with urinary diversion and is considered the preferred treatment option for participants who are considered surgical candidates. Study consists of a Screening phase, Treatment phase and follow-up phase. The total duration of study will be up to 2 years and 6 months. Efficacy, safety, pharmacokinetics (PK), and biomarkers will be assessed at specific time points during this study.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
163
Inclusion Criteria
  • Histologically proven, cT2-T4a N0, M0 infiltrating urothelial carcinoma of the bladder. Initial diagnosis must have been within 120 days of randomization date. Participants with variant histologic subtypes are allowed if tumor(s) demonstrate urothelial predominance. However, the presence of small cell or neuroendocrine variants will make a participant ineligible
  • Participants with no residual tumor, or intravesical tumor size of less than or equal to (<=)3 centimeter (cm) following transurethral resection of bladder tumor (TURBT) are eligible; debulking TURBT for any residual disease is encouraged but not mandated. Participants with persistent tumors greater than (>)3 cm at screening must undergo a second debulking, re-staging TURBT. Participants will be ineligible if any individual tumor is >3 cm after debulking TURBT
  • Deemed eligible for and willing to undergo RC by the operating urologist
  • Eastern Cooperative Oncology Group (ECOG) performance status Grade 0 or 1
  • Thyroid function tests within normal range or stable on hormone supplementation per investigator assessment. Investigators may consult an endocrinologist for participant eligibility assessment in the case of equivocal or marginal tests results
  • All adverse events associated with any prior surgery must have resolved to common terminology criteria for adverse events (CTCAE) version 5.0 Grade less than (<) 2 prior to randomization
Exclusion Criteria
  • Must not have received prior systemic chemotherapy, targeted small molecule therapy, or radiation therapy within 2 weeks prior to starting study treatment
  • Participants must not have evidence of cT4b, or N1-3, or M1 disease based on central radiology staging (chest, abdomen, and pelvis must be performed using computed tomography [CT] or magnetic resonance imaging [MRI]) within 42 days prior to randomization
  • Presence of any bladder or urethral anatomic feature that, in the opinion of the Investigator, may prevent the safe placement, indwelling use, or removal of TAR-200
  • Prior systemic chemotherapy for urothelial cell carcinoma of the bladder at any time
  • Currently participating or has participated in a study of an investigational agent and received study therapy or investigational device within 4 weeks prior to enrollment
  • Participants with evidence of bladder perforation during diagnostic cystoscopy. Participant is eligible if perforation has resolved prior to dosing

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Cohort 2: CetrelimabCetrelimabParticipants will receive cetrelimab.
Cohort 1: TAR-200 + CetrelimabTAR-200Participants will receive TAR-200 in combination with cetrelimab.
Cohort 1: TAR-200 + CetrelimabCetrelimabParticipants will receive TAR-200 in combination with cetrelimab.
Primary Outcome Measures
NameTimeMethod
Percentage of Participants with Pathologic Complete Response (pCR)Up to Week 15

Percentage of participants with a pathologic complete response (pCR) or no evidence of pathologic intravesical disease and nodal involvement (ypT0N0) derived from analysis of radical cystectomy (RC) bladder specimen will be reported.

Secondary Outcome Measures
NameTimeMethod
Recurrence-Free Survival (RFS)Up to Week 108

RFS is defined as the time from first dose of any study treatment to first radiologic (as assessed by response evaluation criteria in solid tumors \[RECIST\] 1.1 criteria) or histologic evidence of nodal or metastatic disease or death due to any cause.

Number of Participants with Adverse Events (AEs) by Grades According to Common Terminology Criteria for Adverse Events (CTCAE)Up to Week 108

Number of participants with AEs by severity grade as assessed by CTCAE version 5 will be reported. Grade refers to the severity of AE as follows: Grade 1- Mild; Grade 2- Moderate; Grade 3- Severe; Grade 4- Life-threatening; Grade 5- Death related to adverse event.

Number of Participants with Change from Baseline in Laboratory AbnormalitiesUp to Week 108

Number of participants with change from baseline in laboratory abnormalities will be reported. Severity will be graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 5.0. Severity scale ranges from Grade 1 (Mild) to Grade 5 (Death). Grade 1= Mild, Grade 2= Moderate, Grade 3= Severe, Grade 4= Life-threatening, and Grade 5= Death related to adverse event.

Trial Locations

Locations (108)

Pusan National University Yangsan Hospital

🇰🇷

Yangsan-si, Korea, Republic of

Ziekenhuisgroep Twente

🇳🇱

Almelo, Netherlands

Haga ziekenhuis

🇳🇱

Den Haag, Netherlands

Radboud Umcn

🇳🇱

Nijmegen, Netherlands

Canisius-Wilhelmina Ziekenhuis

🇳🇱

Nijmegen, Netherlands

Hosp Univ A Coruna

🇪🇸

A Coruna, Spain

Fund. Puigvert

🇪🇸

Barcelona, Spain

Hosp. Univ. San Cecilio

🇪🇸

Granada, Spain

Clinica Univ. de Navarra

🇪🇸

Madrid, Spain

Hospital Universitario 12 de Octubre

🇪🇸

Madrid, Spain

Hosp Virgen de La Victoria

🇪🇸

Málaga, Spain

Hosp. Univ. Marques de Valdecilla

🇪🇸

Santander, Spain

Barts Health NHS Trust

🇬🇧

London, United Kingdom

Lancashire Teaching Hospitals NHS Foundation Trust Royal Preston Hospital

🇬🇧

Preston, United Kingdom

Winship Cancer Institute Emory University

🇺🇸

Atlanta, Georgia, United States

DuPage Medical Group

🇺🇸

Lisle, Illinois, United States

Urology of Indiana

🇺🇸

Indianapolis, Indiana, United States

First Urology

🇺🇸

Jeffersonville, Indiana, United States

Korea University Anam Hospital

🇰🇷

Seoul, Korea, Republic of

Seoul National University Hospital

🇰🇷

Seoul, Korea, Republic of

Severance Hospital

🇰🇷

Seoul, Korea, Republic of

Gangnam Severance Hospital

🇰🇷

Seoul, Korea, Republic of

The Catholic University of Korea Seoul St Mary s Hospital

🇰🇷

Seoul, Korea, Republic of

Universitaetsklinikum Halle Saale

🇩🇪

Halle Saale, Germany

University of Alabama at Birmingham

🇺🇸

Birmingham, Alabama, United States

Urological Associates of Southern Arizona, P.C.

🇺🇸

Tucson, Arizona, United States

UAMS Winthrop P. Rockefeller Cancer Institute

🇺🇸

Little Rock, Arkansas, United States

Arkansas Urology

🇺🇸

Little Rock, Arkansas, United States

City of Hope

🇺🇸

Duarte, California, United States

Genesis Research

🇺🇸

San Diego, California, United States

Colorodo Urology- St. Anthony Hospital

🇺🇸

Golden, Colorado, United States

Marien hospital Herne

🇩🇪

Herne, Germany

Universitatsklinikum Munster

🇩🇪

Muenster, Germany

University of Florida Health Jacksonville

🇺🇸

Jacksonville, Florida, United States

Mayo Clinic

🇺🇸

Rochester, Minnesota, United States

Baptist Hospital of Miami

🇺🇸

Miami, Florida, United States

University of Louisville - James Graham Brown Cancer Center

🇺🇸

Louisville, Kentucky, United States

University Of Maryland Medical Center

🇺🇸

Baltimore, Maryland, United States

Penn Medicine - PerelmanCenter for Advanced Medicine

🇺🇸

Baltimore, Maryland, United States

Brigham and Women's Hospital

🇺🇸

Boston, Massachusetts, United States

Michigan Institute of Urology, PC

🇺🇸

Troy, Michigan, United States

University Of Minnesota

🇺🇸

Minneapolis, Minnesota, United States

Ellis Fischel Cancer Center

🇺🇸

Columbia, Missouri, United States

Washington University School Of Medicine - Center For Advanced Medicine (CAM)

🇺🇸

Saint Louis, Missouri, United States

David C. Pratt Cancer Center

🇺🇸

Saint Louis, Missouri, United States

Robert Wood Johnson University Hospital

🇺🇸

New Brunswick, New Jersey, United States

Mount Sinai Queens Infusion Center

🇺🇸

Astoria, New York, United States

Montefiore Medical Center

🇺🇸

Bronx, New York, United States

New York University Langone Medical Center

🇺🇸

New York, New York, United States

Memorial Sloan Kettering Cancer Center

🇺🇸

New York, New York, United States

SUNY Upstate Medical University

🇺🇸

Syracuse, New York, United States

Associated Medical Professionals

🇺🇸

Syracuse, New York, United States

Wake Forest University Baptist Medical Center (WFUBMC) - Comprehensive Cancer Center

🇺🇸

Winston-Salem, North Carolina, United States

The Ohio State University

🇺🇸

Columbus, Ohio, United States

MidLantic Urology

🇺🇸

Bala-Cynwyd, Pennsylvania, United States

University Of Pittsburgh Medical Center UPMC Hillman Cancer Center

🇺🇸

Pittsburgh, Pennsylvania, United States

Carolina Urologic Research Center

🇺🇸

Myrtle Beach, South Carolina, United States

Urology Associates

🇺🇸

Nashville, Tennessee, United States

Houston Metro Urology

🇺🇸

Houston, Texas, United States

Urology San Antonio Research

🇺🇸

San Antonio, Texas, United States

Huntsman Cancer Institute

🇺🇸

Salt Lake City, Utah, United States

University of Washington School of Medicine

🇺🇸

Seattle, Washington, United States

AZ Sint Jan Brugge Oostende AV

🇧🇪

Brugge, Belgium

Algemeen Ziekenhuis Sint-Jan

🇧🇪

Brugge, Belgium

Ziekenhuis Oost-Limburg

🇧🇪

Genk, Belgium

Hopital de Jolimont

🇧🇪

Haine Saint Paul La Louviere, Belgium

ZNA Jan Palfijn

🇧🇪

Merksem, Belgium

Centre Interuniversitaire Ambroise Pare - Ambroise Paré

🇧🇪

Mons, Belgium

Clinique Tivoli Ducos

🇫🇷

Bordeaux, France

ICH Hopital A. Morvan

🇫🇷

Brest, France

Hopital Henri Mondor

🇫🇷

Creteil, France

Hôpital Privé Le Bois

🇫🇷

Lille, France

Polyclinique de Limoges - Francois Chenieux

🇫🇷

Limoges, France

Hopital de la Timone

🇫🇷

Marseille, France

CHU Montpellier

🇫🇷

Montpellier, France

CHU Nîmes

🇫🇷

Nimes, France

Hopital Bichat Claude Bernard

🇫🇷

Paris Cedex 18, France

Hopital Europeen Georges-Pompidou

🇫🇷

Paris, France

Hospices Civils de Lyon HCL

🇫🇷

Pierre Bénite, France

Clinical La Croix Du Sud - Ramsay Santé

🇫🇷

Quint-Fonsegrives, France

HIA se Sainte-Anne - Toulon

🇫🇷

Toulon, France

Clinique Pasteur

🇫🇷

Toulouse, France

Vivantes Klinikum Am Urban

🇩🇪

Berlin-Kreuzberg, Germany

Staedtisches Klinikum Braunschweig

🇩🇪

Braunschweig, Germany

Agaplesion Frankfurter Diakonie Kliniken GmbH, Markus Krankenhaus

🇩🇪

Frankfurt am Main, Germany

Rambam Health Care Campus

🇮🇱

Haifa, Israel

Carmel Medical Center

🇮🇱

Haifa, Israel

Hadassah Medical Center

🇮🇱

Jerusalem, Israel

Rabin Medical Center - Hasharon Hospital

🇮🇱

Petah Tikva, Israel

The Chaim Sheba Medical Center

🇮🇱

Ramat Gan, Israel

Tel Aviv Sourasky Medical Center

🇮🇱

Tel Aviv Yafo, Israel

Ospedale San Giuseppe Moscati di Avellino

🇮🇹

Avellino, Italy

Ospedale Civile Ramazzini

🇮🇹

Carpi, Italy

SPDC Villa Scassi

🇮🇹

Genova, Italy

IRCCS Ospedale San Raffaele

🇮🇹

Milano, Italy

Istituto Dei Tumori Di Milano

🇮🇹

Milano, Italy

Istituto Europeo di Oncologia

🇮🇹

Milano, Italy

Istituto Nazionale Tumori Fondazione G. Pascale

🇮🇹

Napoli, Italy

Azienda Ospedaliero Universitaria Pisana

🇮🇹

Pisa, Italy

ASL Napoli 2 Nord-SM delle Grazie Hospital

🇮🇹

Pozzuoli, Italy

Istituto Nazionale Tumori Regina Elena

🇮🇹

Roma, Italy

IRCCS Istituto Clinico Humanitas

🇮🇹

Rozzano, Italy

Azienda Ospedaliera Universitaria Citta della Salute e della Scienza di Torino

🇮🇹

Torino, Italy

Inje University Haeundae Paik Hospital

🇰🇷

Busan, Korea, Republic of

Kyungpook National University Chilgok Hospital

🇰🇷

Daegu, Korea, Republic of

Keimyung University Dongsan Hospital

🇰🇷

Daegu, Korea, Republic of

Samsung Medical Center

🇰🇷

Gangnam Gu, Korea, Republic of

National Cancer Center

🇰🇷

Goyang-Si, Korea, Republic of

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