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Spots Global Cancer Trial Database for ADSTILADRIN (=INSTILADRIN) in Patients With High Grade, Bacillus Calmette-Guerin (BCG) Unresponsive Non-Muscle Invasive Bladder Cancer (NMIBC)

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Trial Identification

Brief Title: ADSTILADRIN (=INSTILADRIN) in Patients With High Grade, Bacillus Calmette-Guerin (BCG) Unresponsive Non-Muscle Invasive Bladder Cancer (NMIBC)

Official Title: A Phase III, Open Label Study to Evaluate the Safety and Efficacy of INSTILADRIN® (rAd-IFN)/Syn3) Administered Intravesically to Patients With High Grade, BCG Unresponsive Non-Muscle Invasive Bladder Cancer (NMIBC)

Study ID: NCT02773849

Interventions

ADSTILADRIN

Study Description

Brief Summary: Previous multi-dose Phase I and Phase II clinical studies have demonstrated that ADSTILADRIN is a safe and effective treatment for BCG-refractory and recurrent NMIBC. This Phase III study is designed to expand those observations using a high dose of ADSTILADRIN in patients that are "BCG Unresponsive" which refers to patients with high-grade NMIBC who are unlikely to benefit from and should not receive further intravesical BCG.

Detailed Description: Recombinant IFN alpha2b has pleiotropic effects that contribute to antitumor activity in Non-Muscle Invasive Bladder Cancer (NMIBC). ADSTILADRIN is a non-replicating adenovirus vector harboring the human IFN alpha2b gene. When combined with the excipient Syn3, intravesical administration of the rAd-IFN results in transduction of the virus into the epithelial cell lining in the bladder. The IFN alpha2b gene is incorporated into the cellular DNA resulting in the synthesis and expression of large amounts of IFN alpha2b protein. Clinical studies have confirmed that IFN alpha2b protein can be measured in the urine of patients treated with ADSTILADRIN within 24 hours after dosing.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Banner MD Anderson Cancer Center, Gilbert, Arizona, United States

Keck School of Medicine at USC Medical Center, Los Angeles, California, United States

The Urology Center of Colorado, Denver, Colorado, United States

University of Florida - UF Health Davis Center Pavilion and Shands Med Plaza, Gainesville, Florida, United States

H. Lee Moffitt Cancer Center & Research Institute, Tampa, Florida, United States

Emory University School of Medicine, Atlanta, Georgia, United States

University of Chicago - Comprehensive Cancer Research Center, Chicago, Illinois, United States

Ochsner Clinic Foundation, New Orleans, Louisiana, United States

Johns Hopkins Kimmel Cancer Center, Baltimore, Maryland, United States

University of Michigan, Ann Arbor, Michigan, United States

Spectrum Health Medical Group, Grand Rapids, Michigan, United States

University of Minnesota, Minneapolis, Minnesota, United States

Mayo Clinic - Rochester, Rochester, Minnesota, United States

Washington University School of Medicine, Saint Louis, Missouri, United States

Delaware Valley Urology, LLC, Voorhees, New Jersey, United States

Montefiore Medical Center, Bronx, New York, United States

SUNY Upstate Medical Center, Syracuse, New York, United States

University of North Carolina (UNC) - Chapel Hill, Chapel Hill, North Carolina, United States

Duke University, Durham, North Carolina, United States

The University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, United States

Penn State Milton S. Hershey Medical Center, Hershey, Pennsylvania, United States

The Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, United States

Thomas Jefferson University, Philadelphia, Pennsylvania, United States

Regional Urology, Greenville, South Carolina, United States

Carolina Urologic research Center, Myrtle Beach, South Carolina, United States

Vanderbilt University Medical Center Dept. of Urologic Surgery, Nashville, Tennessee, United States

University of Texas Southwestern Medical Center, Dallas, Texas, United States

Baylor College of Medicine, Houston, Texas, United States

MD Anderson Cancer Center, Houston, Texas, United States

The Univ. of Texas Health Science Center at San Antonio, San Antonio, Texas, United States

University of Virginia Health System, Charlottesville, Virginia, United States

Urology of Virginia, Virginia Beach, Virginia, United States

West Virginia University Cancer Institute, Morgantown, West Virginia, United States

University of Wisconsin - Madison, Madison, Wisconsin, United States

Contact Details

Name: Stephen Boorjian, MD

Affiliation: Mayo Clinic

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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