RecruitingPhase 1Phase 2NCT04752722

LEGEND Study: EG-70 in NMIBC Patients BCG-Unresponsive and High-Risk NMIBC Incompletely Treated With BCG or BCG-Naïve

A Phase 1/2 Study of EG-70 as an Intravesical Administration to Patients With BCG Unresponsive Non-Muscle Invasive Bladder Cancer (NMIBC) and High-Risk NMIBC Patients Who Are BCG Naïve or Received Incomplete BCG Treatment


Sponsor

enGene, Inc.

Enrollment

350 participants

Start Date

Apr 22, 2021

Study Type

INTERVENTIONAL

Conditions

Summary

This study will evaluate the safety and efficacy of intravesical administration of EG-70 in the bladder and its effect on bladder tumors in patients with NMIBC. This study study consists of two phases; a Phase 1 dose-escalation to establish safety and recommended the phase 2 dose, followed by a Phase 2 study to establish how effective the treatment is. The Study will include patients with NMIBC with Cis for whom BCG therapy is unresponsive and patients with NMIBC with Cis who are BCG-naïve or inadequately treated.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a new drug called EG-70 for patients with non-muscle-invasive bladder cancer (NMIBC) — an early stage of bladder cancer — in people who have not responded well to BCG treatment (a standard bladder cancer therapy) or who have never received BCG. **You may be eligible if...** - You have non-muscle-invasive bladder cancer (NMIBC) - You have not responded to prior BCG treatment (BCG-unresponsive), OR you have not completed a full course of BCG, OR you have never received BCG - You are not a candidate for, or have declined, bladder removal surgery (cystectomy) **You may NOT be eligible if...** - Your bladder cancer has invaded the muscle or spread elsewhere - You are a candidate for and willing to undergo bladder removal surgery Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGEG-70 (phase 1)

Patients will receive up to four cycles of EG-70 administered as a bladder instillation of a 50 mL volume of study drug via catheter with a targeted retention time of 60 minutes.One cycle lasts approximately 12 weeks and consists of either a 2-dose (Day 1 and Day 8) or 4-dose (Day 1, Day 8, Day 29 and Day 36) regimen.

DRUGEG-70 (phase 2)

Patients will receive during Treatment Period, up to 4 cycles of EG-70 at the RP2D defined in Phase 1 administered as a bladder instillation of a 50 mL volume of study drug via catheter with a targeted retention time of 60 minutes. One cycle lasts approximately 12 weeks. For Maintenance treatment 2 doses of EG-70 will be administered as a bladder instillation per 12-week cycle.


Locations(101)

The University of Alabama at Birmingham Clinical Research Unit (CRU)

Birmingham, Alabama, United States

Mayo Clinic

Scottsdale, Arizona, United States

Urological Associates of South Arizona

Tucson, Arizona, United States

Arkansas Urology

Little Rock, Arkansas, United States

University of California - Irvine Medical Center

Irvine, California, United States

UC San Diego Moores Cancer Center

La Jolla, California, United States

USC/Norris Comprehensive Cancer Center

Los Angeles, California, United States

Tower Urology

Los Angeles, California, United States

Om Research

San Diego, California, United States

Colorado Clinical Research

Lakewood, Colorado, United States

The George Washington Medical Faculty Associates

Washington D.C., District of Columbia, United States

University of Florida

Jacksonville, Florida, United States

Sylvester Comprehensive Cancer Center / University of Miami Hospital and Clinics

Miami, Florida, United States

Emory University

Atlanta, Georgia, United States

Rush University Medical Center

Chicago, Illinois, United States

Urology of Indiana

Greenwood, Indiana, United States

University of Kansas Medical Center

Kansas City, Kansas, United States

John Hopkins Hospital

Baltimore, Maryland, United States

Chesapeake Urology Research Associates

Hanover, Maryland, United States

Brigham and Women's Hospital

Boston, Massachusetts, United States

Henry Ford Health System

Detroit, Michigan, United States

Corewell Health Medical Group and Spectrum Health Hospitals

Grand Rapids, Michigan, United States

University of Minnesota

Minneapolis, Minnesota, United States

Mayo Clinic

Rochester, Minnesota, United States

Rutgers Cancer Institute of New Jersey

New Brunswick, New Jersey, United States

New Jersey Urology, LLC

Voorhees Township, New Jersey, United States

Albany Medical College

Albany, New York, United States

Mount Sinai Medical Center

New Haven, New York, United States

Laura & Isaac Perlmutter Cancer Center at NYU Langone Health

New York, New York, United States

Associated Medical Professionals of NY,

Syracuse, New York, United States

UNC Chapel Hill Hospital

Chapel Hill, North Carolina, United States

Duke Health - Duke Cancer Center

Durham, North Carolina, United States

Associated Urologists of North Carolina

Raleigh, North Carolina, United States

University of Cincinnati Medical Center

Cincinnati, Ohio, United States

Central Ohio Urology Group

Gahanna, Ohio, United States

Clinical Research Solutions - Helios Clinical Research

Middleburg Heights, Ohio, United States

Oregon Health & Science University (OHSU)

Portland, Oregon, United States

Thomas Jefferson University, Sidney Kimmel Cancer Center

Philadelphia, Pennsylvania, United States

Carolina Urologic Research Center, LLC

Myrtle Beach, South Carolina, United States

Urology Associates, P.C.

Nashville, Tennessee, United States

Vanderbilt Univerity Medical Center

Nashville, Tennessee, United States

Urology Austin

Austin, Texas, United States

UT Southwestern Medical Center

Dallas, Texas, United States

Houston Metro Urology

Houston, Texas, United States

Houston Methodist Hospital - Department of Urology

Houston, Texas, United States

University of Texas - MD Anderson Cancer Center

Houston, Texas, United States

Huntsman Cancer Institute, University of Utah

Salt Lake City, Utah, United States

University of Virginia Comprehensive Cancer Center

Charlottesville, Virginia, United States

Froedtert Hospital / Medical College of Wisconsin

Milwaukee, Wisconsin, United States

Sydney Adventist Hospital

Wahroonga, New South Wales, Australia

Gold Coast University Hospital

Southport, Queensland, Australia

Icon Cancer Center Windsor Gardens

Windsor Gardens, South Australia, Australia

Prostate Cancer Centre

Calgary, Alberta, Canada

Vancouver Prostate Centre

Vancouver, British Columbia, Canada

Nova Scotia Health Authority

Halifax, Nova Scotia, Canada

University Health Network, Princess Margaret Cancer Centre

Toronto, Ontario, Canada

McGill University Health Center - Glen site

Montreal, Quebec, Canada

CHUM Centre Hospitalier de l Universite de Montreal

Montreal, Quebec, Canada

CHU d'Angers

Angers, France

CHU Bordeaux Pellegrin

Bordeaux, France

lnstitut Bergonie 229 Cour de l'Argonne

Bordeaux, France

CHU de Lille

Lille, France

Hospices Civils de Lyon

Lyon, France

Hopital Bichat Claude-Bernard

Paris, France

CHU de Rauen- Hopital Charles Nicolle

Rouen, France

Klinik fur Urologie, Uro-Onkologie, spezielle urologische und Roboter-assistierte Chirurgie Universitatsklinikum Koln (AOR)

Cologne, Germany

Urologicum Duisburg

Duisburg, Germany

Universitaetsklinikum Erlangen

Erlangen, Germany

Urologie Neandertal Mettmann

Mettmann, Germany

Studienpraxis Urologie

Nürtingen, Germany

Universitaetsklinikum Tubingen

Tübingen, Germany

Clinic Unit of Urology, IRCCS Ospedale San Raffaele

Milan, MI, Italy

Istituto Europeo di Oncologia

Milan, Italy

Istituto Nazionale Tumori IRCCS Fondazione G. Pascale

Naples, Italy

Fondazione Policlinico Universitario "A.Gemelli" IRCCS, Largo

Rome, Italy

Azienda Ospedaliero-Universitaria Sant'Andrea

Rome, Italy

UOC Urologia, IFO- lstituto Tumori "Regina Elena"

Rome, Italy

Ospedelae Molinette San Giovanni Battista Di Torino

Torino, Italy

Seoul National University Bundang Hospital

Seongnam, Gyunggi-do, South Korea

Chonnam National University Hwasun Hospital

Hwasun, Jeollanam-do, South Korea

Seoul National University Hospital

Seoul, South Korea

Severance Hospital, Yonsei University Health System

Seoul, South Korea

The Catholic University of Korea, Soul St. Mary's Hospital

Seoul, South Korea

IOB - Hospital Quironsalud Barcelona

Barbera Del Valles, Spain

Fundacio Puigvert

Barcelona, Spain

Hospital Clinic Barcelona

Barcelona, Spain

Hospital Germans Trias i Pujol

Barcelona, Spain

Hospital Universitari de Bellvitge

L'Hospitalet de Llobregat, Spain

Hospital General Universitario Gregorio Maranon

Madrid, Spain

Hospital Universitario 12 de Octubre

Madrid, Spain

Hospital Universitario La Paz

Madrid, Spain

Hospital Quironsalud Madrid (Next Oncology)

Madrid, Spain

Hospital Universitario Infanta Sofia

Madrid, Spain

Hospital General Universitario Morales Meseguer

Murcia, Spain

Hospital Universitario Marqués de Valdecilla,

Santander, Spain

Kaohsiung Medical University Chung-Ho Memorial Hospital

Kaohsiung City, Taiwan

China Medical University Hospital

Taichung, Taiwan

Taichung Veterans General Hospital

Taichung, Taiwan

Chi Mei Medical Center

Tainan, Taiwan

National Taiwan University Hospital

Taipei, Taiwan

The Royal Marsden NHS Foundation Trust

London, United Kingdom

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NCT04752722


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