Safety and Efficacy Study of Intravesical Instillation of TARA-002 in Adults With High-grade Non-muscle Invasive Bladder Cancer
Conditions
Non-muscle Invasive Bladder Cancer
Simple summaryAI-assisted
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Locations
Urology Centers of Alabama, Homewood, Alabama, United States
Contact: Study coordinator (Use Central Contact)Mayo Clinic, Phoenix, Arizona, United States
Contact: Study coordinator (Use Central Contact)East Valley Urology Center of Arizona, Queen Creek, Arizona, United States
Contact: Study coordinator (Use Central Contact)Arkansas Urology, Little Rock, Arkansas, United States
Contact: Study coordinator (Use Central Contact)Michael Oefelein Clinical Trials, Bakersfield, California, United States
Contact: Study coordinator (Use Central Contact)Urology Group of Southern California, Los Angeles, California, United States
University of California Irvine Medical Center, Orange, California, United States
Contact: Study coordinator (Use Central Contact)Genesis Research, San Diego, California, United States
Genesis Research LLC, Torrance, California, United States
Contact: Study coordinator (Use Central Contact)Colorado University - Anshutz, Aurora, Colorado, United States
Contact: Study coordinator (Use Central Contact)AdventHealth Medical Group Urology of Denver, Denver, Colorado, United States
Contact: Study coordinator (Use Central Contact)Advanced Urology, Lakewood, Colorado, United States
Contact: Study coordinator (Use Central Contact)Urology Associates of Denver, Lone Tree, Colorado, United States
Contact: Study coordinator (Use Central Contact)University of Florida Health Jacksonville, Gainesville, Florida, United States
Mayo Clinic, Jacksonville, Florida, United States
Contact: Study coordinator (Use Central Contact)Comprehensive Urologic Care, Lake Barrington, Illinois, United States
Contact: Study coordinator (Use Central Contact)Southern Urology, Lafayette, Louisiana, United States
Contact: Study coordinator (Use Central Contact)Ochsner Health LSU - Regional Urology, Shreveport, Louisiana, United States
Brigham and Women's Hospital, Boston, Massachusetts, United States
Contact: Study coordinator (Use Central Contact)Minnesota Urology, Woodbury, Bloomington, Minnesota, United States
Contact: Study coordinator (Use Central Contact)Mayo Clinic, Rochester, Minnesota, United States
Contact: Study coordinator (Use Central Contact)Renown Regional Medical Center, St Louis, Missouri, United States
Contact: Study coordinator (Use Central Contact)Specialty Clinic Research of St. Louis, St Louis, Missouri, United States
Contact: Study coordinator (Use Central Contact)AccuMed Research Associates, Garden City, New York, United States
Laura & Isaac Perlmutter Cancer Center - NYU Langone Health, New York, New York, United States
Contact: Study coordinator (Use Central Contact)University of Rochester, Department of Urology, Rochester, New York, United States
Contact: Study coordinator (Use Central Contact)Montefiore Medical Center, The Bronx, New York, United States
Contact: Study coordinator (Use Central Contact)University of Toledo, Toledo, Ohio, United States
University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States
Contact: Study coordinator (Use Central Contact)Carolina Urologic Research Center, Myrtle Beach, South Carolina, United States
Contact: Study coordinator (Use Central Contact)Conrad Person Clinic, Memphis, Tennessee, United States
Contact: Study coordinator (Use Central Contact)Urology Associates PC, Nashville, Tennessee, United States
Contact: Study coordinator (Use Central Contact)Amarillo Urology Research, Amarillo, Texas, United States
Urology Partners of North Texas, Arlington, Texas, United States
Contact: Study coordinator (Use Central Contact)Urology Austin, LLC, Austin, Texas, United States
Contact: Study coordinator (Use Central Contact)Houston Metro Urology, Houston, Texas, United States
Contact: Study coordinator (Use Central Contact)Houston Methodist Hospital, Houston, Texas, United States
Contact: Study coordinator (Use Central Contact)Clinical Trial Network, Houston, Texas, United States
UT Health San Antonio, San Antonio, Texas, United States
Contact: Study coordinator (Use Central Contact)Virginia Urology, Richmond, Virginia, United States
Contact: Study coordinator (Use Central Contact)Spokane Urology, Spokane, Washington, United States
Contact: Study coordinator (Use Central Contact)Hospital Italiano de Buenos Aires (HIBA), Buenos Aires, Argentina
Contact: Study coordinator (Use Central Contact)Hospital Britanico de Buenos Aires, Buenos Aires, Argentina
Contact: Study coordinator (Use Central Contact)Centro Argentino de Urologia, CABA, Argentina
Contact: Study coordinator (Use Central Contact)Hospital Sirio Libanes, CABA, Argentina
Contact: Study coordinator (Use Central Contact)Centro Urologico Profesor Bengio SA, Córdoba, Argentina
Contact: Study coordinator (Use Central Contact)CEMAIC, Córdoba, Argentina
Contact: Study coordinator (Use Central Contact)Clinica Privada Independencia, Munro, Argentina
Contact: Study coordinator (Use Central Contact)Kyushu University Hospital, Nova Lima, Minas Gerais, Brazil
Contact: Study coordinator (Use Central Contact)Office of Lucas Nougeria MA, Nova Lima, Minas Gerais, Brazil
Contact: Study coordinator (Use Central Contact)Santa Casa de Misericordia de Porto Alegre, Porto Alegre, Rio Grande do Sul, Brazil
Contact: Study coordinator (Use Central Contact)Nucleo de Pesquisa Clinica do Rio Grande so Sul, Porto Alegre, Rio Grande do Sul, Brazil
Contact: Study coordinator (Use Central Contact)Centro de Urologia Avancada, Porto Alegre, Rio Grande do Sul, Brazil
Contact: Study coordinator (Use Central Contact)Hospital de Clinicas da UNICAMP, Campinas, São Paulo, Brazil
Contact: Study coordinator (Use Central Contact)Instituto Dor de Pesquisa e Ensino, Jardim Paulista, São Paulo, Brazil
Contact: Study coordinator (Use Central Contact)Faculdade de Medicina ABC-CEPHO, Santo André, São Paulo, Brazil
Contact: Study coordinator (Use Central Contact)Exdeo Clinical Research Inc, Abbotsford British Columbia, British Columbia, Canada
Jonathan Giddes Medicine Professional Corporation, Brampton, Ontario, Canada
Sunnybrook Research Institute, Toronto, Ontario, Canada
UHN Princess Margaret Cancer Centre Princess Margaret Hospital, Toronto, Ontario, Canada
Komaki City Hospital, Komaki-shi, Aichi-ken, Japan
Contact: Study coordinator (Use Central Contact)Japanese Red Cross Aichi Medical Center Nayoya Daiichi, Nagoya, Aichi-ken, Japan
Contact: Study coordinator (Use Central Contact)Fuji City General Hospital, Sakura-shi, Chiba, Japan
Contact: Study coordinator (Use Central Contact)Kyushu University Hospital, Fukuoka, Fukuoka, Japan
Contact: Study coordinator (Use Central Contact)Hyogo Prefectural Amagasaki General Medical Center, Amagasaki-shi, Hyōgo, Japan
Contact: Study coordinator (Use Central Contact)Hitachi General Hospital, Hitachi-shi, Ibaraki, Japan
Contact: Study coordinator (Use Central Contact)Niigata Cancer Center Hospital, Niigata, Niigata, Japan
Contact: Study coordinator (Use Central Contact)Japanese Red Cross Osaka Hospital, Osaka, Osaka, Japan
Contact: Study coordinator (Use Central Contact)Toho University Medical Center Sakura Hospital, Fuji-shi, Shizuoka, Japan
Contact: Study coordinator (Use Central Contact)Toyama University Hospital, Toyama, Toyama, Japan
Contact: Study coordinator (Use Central Contact)Arensia Kapitanivka - PPDS, Kapitanivka, Ukraine
Contact: Study coordinator (Use Central Contact)
Study leads
Chief Scientific Operations Officer
Study Director
Protara Therapeutics