Back to Trials
NCT05951179PHASE2Recruiting

Safety and Efficacy Study of Intravesical Instillation of TARA-002 in Adults With High-grade Non-muscle Invasive Bladder Cancer

Protara Therapeutics

Start Date

9/15/2023

Completion Date

3/1/2032

Summary

TARA-002-101-Ph2 is an open-label study to investigate the safety and efficacy of intravesical instillation of TARA-002 in adults 18 years of age or older with high-grade CIS NMIBC (± Ta/T1). The purpose of this Phase 2 study (TARA-002-101-Ph2) is to further assess the safety and efficacy of TARA-002 at the RP2D which has been established in the Phase 1a dose finding study (TARA-002-101-Ph1a). This Phase 2 study includes participants with CIS NMIBC (± Ta/T1) with active disease, defined as disease present at last tumor evaluation (within 3 months) prior to signing the ICF. Participants will be enrolled into one of 2 cohorts: Cohort A: * Participants with CIS (± Ta/T1) who are BCG naive, or * Participants with CIS (± Ta/T1) who are BCG exposed and have not received intravesical BCG for at least 24 months prior to the most recent CIS diagnosis Cohort B: * Participants who are BCG unresponsive

Eligibility Criteria

Age Range: 18 years to No maximum

Inclusion Criteria: * Male or female participants 18 years of age or older at the time of signing informed consent * Participants who have voluntarily given written informed consent after the nature of the study has been explained according to applicable requirements prior to study entry * Central histologic confirmation of high-grade non-muscle invasive CIS (± Ta/T1) with active disease * Participants who are BCG naive, or participants who are BCG exposed and have not received intravesical BCG for at least 24 months prior to the most recent CIS diagnosis (Cohort A). Participants with CIS (± Ta/T1) who are BCG unresponsive. Exclusion Criteria: * Penicillin allergy (participants with a questionable history of allergy to penicillin will undergo penicillin blood allergy testing via central laboratory * Central confirmed variant histology * Concomitant prostatic or upper tract urothelial involvement per Investigator's assessment * Nodal and metastatic disease are excluded if they existed at any time (whether present or in the past) * Any history of ≥ T2 bladder cancer that existed at any point in time in the participant's history For more information on eligibility criteria, please contact the Sponsor

Interventions

BIOLOGICAL

TARA-002

Interested in This Trial?

Contact the trial locations directly using the information below to learn more about enrollment.

Expressing interest lets you review the study and consent before we connect you with the research site.

Conditions

Non-muscle Invasive Bladder Cancer

Locations

Urology Centers of Alabama

Homewood, Alabama 35209

United States

Mayo Clinic

Phoenix, Arizona 85054

United States

East Valley Urology Center of Arizona

Queen Creek, Arizona 85140

United States

Arkansas Urology

Little Rock, Arkansas 72211

United States

Michael Oefelein Clinical Trials

Bakersfield, California 93301

United States

Urology Group of Southern California

Los Angeles, California 90017

United States

University of California Irvine Medical Center

Orange, California 92697

United States

Genesis Research

San Diego, California 92123

United States

Genesis Research LLC

Torrance, California 90505

United States

Colorado University - Anshutz

Aurora, Colorado 80045

United States

AdventHealth Medical Group Urology of Denver

Denver, Colorado 80211

United States

Advanced Urology

Lakewood, Colorado 80228

United States

Urology Associates of Denver

Lone Tree, Colorado 80124

United States

University of Florida Health Jacksonville

Gainesville, Florida 32611

United States

Mayo Clinic

Jacksonville, Florida 32224

United States

Comprehensive Urologic Care

Lake Barrington, Illinois 60010

United States

Southern Urology

Lafayette, Louisiana 70508

United States

Ochsner Health LSU - Regional Urology

Shreveport, Louisiana 71105

United States

Brigham and Women's Hospital

Boston, Massachusetts 02115

United States

Minnesota Urology, Woodbury

Bloomington, Minnesota 55425

United States

Mayo Clinic

Rochester, Minnesota 55905

United States

Renown Regional Medical Center

St Louis, Missouri 63110

United States

Specialty Clinic Research of St. Louis

St Louis, Missouri 63141

United States

AccuMed Research Associates

Garden City, New York 11530

United States

Laura & Isaac Perlmutter Cancer Center - NYU Langone Health

New York, New York 10016

United States

University of Rochester, Department of Urology

Rochester, New York 14642

United States

Montefiore Medical Center

The Bronx, New York 10467

United States

University of Toledo

Toledo, Ohio 43606

United States

University of Pittsburgh Medical Center

Pittsburgh, Pennsylvania 15213

United States

Carolina Urologic Research Center

Myrtle Beach, South Carolina 29572

United States

Conrad Person Clinic

Memphis, Tennessee 38128

United States

Urology Associates PC

Nashville, Tennessee 37209

United States

Amarillo Urology Research

Amarillo, Texas 79106

United States

Urology Partners of North Texas

Arlington, Texas 76017

United States

Urology Austin, LLC

Austin, Texas 78745

United States

Houston Metro Urology

Houston, Texas 77027

United States

Houston Methodist Hospital

Houston, Texas 77030

United States

Clinical Trial Network

Houston, Texas 77074

United States

UT Health San Antonio

San Antonio, Texas 78229

United States

Virginia Urology

Richmond, Virginia 23235

United States

Spokane Urology

Spokane, Washington 99202

United States

Hospital Italiano de Buenos Aires (HIBA)

Buenos Aires, C1199ABB

Argentina

Hospital Britanico de Buenos Aires

Buenos Aires, C1280

Argentina

Centro Argentino de Urologia

CABA, C1419

Argentina

Hospital Sirio Libanes

CABA, C1419

Argentina

Centro Urologico Profesor Bengio SA

Córdoba, X5000KPH

Argentina

CEMAIC

Córdoba, X5088

Argentina

Clinica Privada Independencia

Munro, 1605

Argentina

Kyushu University Hospital

Nova Lima, Minas Gerais 34006-059

Brazil

Office of Lucas Nougeria MA

Nova Lima, Minas Gerais 34006-059

Brazil

Santa Casa de Misericordia de Porto Alegre

Porto Alegre, Rio Grande do Sul 90035-070

Brazil

Nucleo de Pesquisa Clinica do Rio Grande so Sul

Porto Alegre, Rio Grande do Sul 90430-001

Brazil

Centro de Urologia Avancada

Porto Alegre, Rio Grande do Sul 91350-200

Brazil

Hospital de Clinicas da UNICAMP

Campinas, São Paulo 13083-970

Brazil

Instituto Dor de Pesquisa e Ensino

Jardim Paulista, São Paulo 01401-002

Brazil

Faculdade de Medicina ABC-CEPHO

Santo André, São Paulo 09060-650

Brazil

Exdeo Clinical Research Inc

Abbotsford British Columbia, British Columbia V2T 1X8

Canada

Jonathan Giddes Medicine Professional Corporation

Brampton, Ontario L6T 4S5

Canada

Sunnybrook Research Institute

Toronto, Ontario M4N 3M5

Canada

UHN Princess Margaret Cancer Centre Princess Margaret Hospital

Toronto, Ontario M5G 1Z5

Canada

Komaki City Hospital

Komaki-shi, Aichi-ken 485-0044

Japan

Japanese Red Cross Aichi Medical Center Nayoya Daiichi

Nagoya, Aichi-ken 435-8511

Japan

Fuji City General Hospital

Sakura-shi, Chiba 285-8741

Japan

Kyushu University Hospital

Fukuoka, Fukuoka 812-8582

Japan

Hyogo Prefectural Amagasaki General Medical Center

Amagasaki-shi, Hyōgo 660-8550

Japan

Hitachi General Hospital

Hitachi-shi, Ibaraki 317-0077

Japan

Niigata Cancer Center Hospital

Niigata, Niigata 961-8566

Japan

Japanese Red Cross Osaka Hospital

Osaka, Osaka 543-855

Japan

Toho University Medical Center Sakura Hospital

Fuji-shi, Shizuoka 417-8567

Japan

Toyama University Hospital

Toyama, Toyama 930-0152

Japan

Arensia Kapitanivka - PPDS

Kapitanivka, 08111

Ukraine