Study Comparing AAA817+ARPI Versus Standard of Care in Adult Participants With PSMA-positive mCRPC

Abroad (travel likely)RecruitingPHASE3

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
  • Stanford University Medical Center, Palo Alto, California, United States

    Contact: Study coordinator (Tiffany Chen) · tiff1221@stanford.edu
    Contact: Principal Investigator (Hong Song)
  • Sansum Clinic, Santa Barbara, California, United States

    Contact: Study coordinator (Megan Martinez) · megan.martinez@sutterhealth.or · 805-563-5800
    Contact: Principal Investigator (Mukul Gupta)
  • Rocky Mountain Cancer Centers, Denver, Colorado, United States

    Contact: Study coordinator (Bethany Glatthar) · Bethany.Glatthar@usoncology.com · 303-839-6530
    Contact: Principal Investigator (Allen Cohn)
  • Baptist Health South, Miami, Florida, United States

    Contact: Study coordinator (Leslie Castaneda) · leslie.castaneda@baptisthealth.net
    Contact: Principal Investigator (Rohan Garje)
  • AdventHealth, Orlando, Florida, United States

    Contact: Study coordinator (Joseph Guzzo) · joseph.guzzo@adventhealth.com · 407-303-3235
    Contact: Principal Investigator (Ravi Shridhar)
  • Northwestern University, Chicago, Illinois, United States

    Contact: Study coordinator (Rachel Hanna Springsdorf) · rachelspringsdorf@northwestern.edu · +1 312 695 1382
    Contact: Principal Investigator (Maha Hussain)
  • Univ Of Iowa Hospitals And Clinics, Iowa City, Iowa, United States

    Contact: Study coordinator (Kellie Bodeker) · kellie-bodeker@uiowa.edu
    Contact: Principal Investigator (Kristin Plichta)
  • University of Kansas Hospital, Kansas City, Kansas, United States

    Contact: Study coordinator (Collin Bruey) · cbruey@kumc.edu
    Contact: Principal Investigator (Xinglei Shen)
  • East Jefferson Hospital, Metairie, Louisiana, United States

    Contact: Study coordinator (Alexandra Lieberman) · alexandra.lieberman@lcmchealth.org
    Contact: Principal Investigator (Alton Oliver Sartor)
  • Dana Farber Cancer Institute, Boston, Massachusetts, United States

    Contact: Study coordinator (Amanda Lilienfeld) · amanda_lilienfeld@dfci.harvard.edu
    Contact: Principal Investigator (Xiao Wei)
  • Wash U School of Medicine, St Louis, Missouri, United States

    Contact: Study coordinator (Collin Welch) · c.welch@wustl.edu
    Contact: Principal Investigator (Jeff Michalski)
  • Nebraska Cancer Specialists, Omaha, Nebraska, United States

    Contact: Study coordinator (Marlene Bridwell) · mbridwell@nebraskacancer.com
    Contact: Principal Investigator (Samuel Mehr)
  • New Jersey Urology LLC, Voorhees Township, New Jersey, United States

    Contact: Study coordinator (Gabriela Mercado) · gmercado3@nj-urology.com · 856-673-1613
    Contact: Principal Investigator (Gordon Brown)
  • Bassett Medical Center, Cooperstown, New York, United States

    Contact: Study coordinator (Peggy Cross) · peggy.cross@bassett.org
    Contact: Principal Investigator (Timothy Korytko)
  • Weill Cornell Medicine NY-Presb, New York, New York, United States

    Contact: Study coordinator (Sarah Yuan) · say7008@med.cornell.edu · 646-962-2535
    Contact: Principal Investigator (Scott Tagawa)
  • University of Rochester Medical Ctr, Rochester, New York, United States

    Contact: Study coordinator (Therese Smudzin) · Therese_Smudzin@urmc.rochester.edu
    Contact: Principal Investigator (Haoming Carl Qiu)
  • Associated Med Professionals of NY, Syracuse, New York, United States

    Contact: Study coordinator (Nathan Forrest) · nathan.forrest@ampofny.com
    Contact: Principal Investigator (Steven Finkelstein)
  • Montefiore Medical Center, The Bronx, New York, United States

    Contact: Study coordinator (Tahrima Chowdhury) · tahchowdhu@montefiore.org · 718-920-2680
    Contact: Principal Investigator (Benjamin A Gartrell)
  • Central Ohio Urology Group, Gahanna, Ohio, United States

    Contact: Study coordinator (Tosha Heineman) · tosha@optimedresearch.com
    Contact: Principal Investigator (Benjamin Martin)
  • MUSC Hollings Cancer Center, Charleston, South Carolina, United States

    Contact: Study coordinator (Alex Jones) · joalex@musc.edu
    Contact: Principal Investigator (Kevin Becker)
  • Carolina Urologic Research Center, Myrtle Beach, South Carolina, United States

    Contact: Study coordinator (Rebecca Floyd) · rebecca.floyd@startresearch.com · 843-839-1679
    Contact: Principal Investigator (Neal D Shore)
  • Urology San Antonio, San Antonio, Texas, United States

    Contact: Study coordinator (Sandra Davila) · sandra.davila@usa-clinicaltrials.com
    Contact: Principal Investigator (Daniel Saltzstein)
  • Woodlands Cancer Institute American Oncology Partners, The Woodlands, Texas, United States

    Contact: Study coordinator (Brittany Rogers) · brittany.rogers@aoncology.com
    Contact: Principal Investigator (Jason Berilgen)
  • Swedish Medical Center, Seattle, Washington, United States

    Contact: Study coordinator (Brianna McNealley) · brianna.mcnealley@swedish.org · 855-922-6237
    Contact: Principal Investigator (Song Zhao)
  • Medical College of Wisconsin, Milwaukee, Wisconsin, United States

    Contact: Study coordinator (Mariah Ziegler) · mziegler@mcw.edu · 414-805-5249
    Contact: Principal Investigator (Deepak Kilari)
  • Novartis Investigative Site, Darlinghurst, New South Wales, Australia

  • Novartis Investigative Site, Adelaide, South Australia, Australia

  • Novartis Investigative Site, São Paulo, São Paulo, Brazil

  • Novartis Investigative Site, São Paulo, São Paulo, Brazil

  • Novartis Investigative Site, Fuzhou, Fujian, China

  • Novartis Investigative Site, Guangzhou, Guangdong, China

  • Novartis Investigative Site, Wuhan, Hubei, China

  • Novartis Investigative Site, Wuhan, Hubei, China

  • Novartis Investigative Site, Nanjing, Jiangsu, China

  • Novartis Investigative Site, Nanjing, Jiangsu, China

  • Novartis Investigative Site, Shenyang, Liaoning, China

  • Novartis Investigative Site, Chengdu, Sichuan, China

  • Novartis Investigative Site, Hangzhou, Zhejiang, China

  • Novartis Investigative Site, Beijing, China

  • Novartis Investigative Site, Beijing, China

  • Novartis Investigative Site, Guangzhou, China

  • Novartis Investigative Site, Shanghai, China

  • Novartis Investigative Site, Shanghai, China

  • Novartis Investigative Site, Shanghai, China

  • Novartis Investigative Site, Tianjin, China

  • Novartis Investigative Site, Hong Kong, Hong Kong

  • Novartis Investigative Site, Gurgaon, Haryana, India

  • Novartis Investigative Site, Bengaluru, Karnataka, India

  • Novartis Investigative Site, Mumbai, Maharashtra, India

  • Novartis Investigative Site, Sapporo, Hokkaido, Japan

  • Novartis Investigative Site, Kobe, Hyōgo, Japan

  • Novartis Investigative Site, Kobe, Hyōgo, Japan

  • Novartis Investigative Site, Yokohama, Kanagawa, Japan

  • Novartis Investigative Site, Chuo Ku, Tokyo, Japan

  • Novartis Investigative Site, Chiba, Japan

  • Novartis Investigative Site, Fukuoka, Japan

  • Novartis Investigative Site, Fukuoka, Japan

  • Novartis Investigative Site, Fukuoka, Japan

  • Novartis Investigative Site, Fukushima, Japan

  • Novartis Investigative Site, Hiroshima, Japan

  • Novartis Investigative Site, Kyoto, Japan

  • Novartis Investigative Site, Singapore, Singapore

  • Novartis Investigative Site, Singapore, Singapore

  • Novartis Investigative Site, Singapore, Singapore

  • Novartis Investigative Site, Seoul, South Korea

  • Novartis Investigative Site, Seoul, South Korea

  • Novartis Investigative Site, Kaohsiung City, Taiwan

  • Novartis Investigative Site, Taipei, Taiwan

  • Novartis Investigative Site, Taoyuan, Taiwan

  • Novartis Investigative Site, Sutton, Surrey, United Kingdom

Study leads
  • Novartis Pharmaceuticals

    Study Director

    Novartis Pharmaceuticals