Long-Term Safety of Lutetium (177Lu) Vipivotide Tetraxetan in Participants With Prostate Cancer

Abroad (travel likely)RecruitingPHASE4

Conditions

Prostate Cancer

Simple summaryAI-assisted

This summary is produced by a language model and is experimental. It may be incomplete or inaccurate and is not a substitute for professional medical advice.

Locations
  • Mayo Clinic Arizona, Scottsdale, Arizona, United States

    Study coordinator · 480-301-8300
    Contact: Principal Investigator (Cassandra Moore)
  • St. Joseph Hospital, Orange, California, United States

    Contact: Principal Investigator (Timothy Byun)
  • Providence Saint Johns Health Ctr, Santa Monica, California, United States

    Contact: Principal Investigator (Przemyslaw Twardowski)
  • University of Colorado, Aurora, Colorado, United States

    Contact: Principal Investigator (Muthiah Nachiappan)
  • Hartford Hospital, Hartford, Connecticut, United States

    Contact: Principal Investigator (Andrew Salner)
  • VA Medical Center, Washington D.C., District of Columbia, United States

    Study coordinator · 202-745-8457
    Contact: Principal Investigator (Frank Liu)
  • Mayo Clinic Jacksonville, Jacksonville, Florida, United States

    Contact: Principal Investigator (Winston Tan)
  • University Cancer and Blood Center LLC, Athens, Georgia, United States

    Study coordinator · 706-353-2990
    Contact: Principal Investigator (Petros Nikolinakos)
  • Parkview Research Center, Fort Wayne, Indiana, United States

    Contact: Principal Investigator (Brian Chang)
  • Tulane Cancer Center, New Orleans, Louisiana, United States

    Study coordinator · 504-585-6077
    Contact: Principal Investigator (Brian Lewis)
  • Ochsner Clinic Foundation, New Orleans, Louisiana, United States

    Study coordinator · 504-842-6044
    Contact: Principal Investigator (Stephen Bardot)
  • Corewell Health William Beaum Hosp, Royal Oak, Michigan, United States

    Contact: Principal Investigator (Andrew Thompson)
  • Mayo Clinic Rochester, Rochester, Minnesota, United States

    Contact: Principal Investigator (Brian Costello)
  • University of Mississippi Med Ctr, Jackson, Mississippi, United States

    Study coordinator · +1 601 815 5374
    Contact: Principal Investigator (John Clark Henegan)
  • Wash U School of Medicine, St Louis, Missouri, United States

    Contact: Study coordinator (Lindsey Mayer) · lindseymayer@wustl.edu
    Contact: Principal Investigator (Hyun Kim)
  • Urology Cancer Center PC, Omaha, Nebraska, United States

    Study coordinator · 402-697-2229
    Contact: Principal Investigator (Luke Nordquist)
  • Nebraska Cancer Specialists, Omaha, Nebraska, United States

    Contact: Principal Investigator (Ralph Hauke)
  • Montefiore Medical Center, The Bronx, New York, United States

    Contact: Principal Investigator (Benjamin A Gartrell)
  • Duke University Medical Center, Durham, North Carolina, United States

    Contact: Principal Investigator (Daniel J George)
  • Cleveland Clinic Foundation, Cleveland, Ohio, United States

    Study coordinator · 216-444-0441
    Contact: Principal Investigator (Shilpa Gupta)
  • Univ of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States

    Contact: Principal Investigator (Leonard Appleman)
  • Univ of Texas Southwest Med Center, Dallas, Texas, United States

    Contact: Principal Investigator (Kevin Courtney)
  • UT Health Science Center, Houston, Texas, United States

    Contact: Principal Investigator (Bo Chen)
  • Onco Hemato Asso of SW Virginia, Roanoke, Virginia, United States

    Study coordinator · 540-774-8660
    Contact: Principal Investigator (David Buck)
  • Novartis Investigative Site, Linz, Austria

  • Novartis Investigative Site, Vienna, Austria

  • Novartis Investigative Site, Ghent, Belgium

  • Novartis Investigative Site, Montreal, Quebec, Canada

  • Novartis Investigative Site, Olomouc, Czechia

  • Novartis Investigative Site, Prague, Czechia

  • Novartis Investigative Site, Lyon, France

  • Novartis Investigative Site, Essen, Germany

  • Novartis Investigative Site, München, Germany

  • Novartis Investigative Site, Rostock, Germany

  • Novartis Investigative Site, Nijmegen, Gelderland, Netherlands

  • Novartis Investigative Site, Maastricht, Limburg, Netherlands

  • Novartis Investigative Site, Delft, South Holland, Netherlands

  • Novartis Investigative Site, L'Hospitalet de Llobregat, Barcelona, Spain

  • Novartis Investigative Site, Sabadell, Barcelona, Spain

  • Novartis Investigative Site, Majadahonda, Madrid, Spain

  • Novartis Investigative Site, Barcelona, Spain

  • Novartis Investigative Site, Barcelona, Spain

  • Novartis Investigative Site, Madrid, Spain

  • Novartis Investigative Site, Madrid, Spain

  • Novartis Investigative Site, Madrid, Spain

  • Novartis Investigative Site, Madrid, Spain

  • Novartis Investigative Site, Valencia, Spain

  • Novartis Investigative Site, Gothenburg, Sweden

  • Novartis Investigative Site, Stockholm, Sweden

  • Novartis Investigative Site, Sutton, Surrey, United Kingdom

  • Novartis Investigative Site, Barnet, United Kingdom

  • Novartis Investigative Site, Cambridge, United Kingdom

  • Novartis Investigative Site, Glasgow, United Kingdom

  • Novartis Investigative Site, Middlesbrough, United Kingdom

Study leads
  • Novartis Pharmaceuticals

    Study Director

    Novartis Pharmaceuticals