CAR-T Long Term Follow Up (LTFU) Study

IsraelRecruitingPHASE3

Conditions

Long Term Safety of Patients Receiving CAR-T in an Eligible Clinical Trial or Managed Access Program

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, Phoenix, Arizona, United States

  • City of Hope National Medical Center, Duarte, California, United States

    Contact: Principal Investigator (Leslie Popplewell)
  • Childrens Hospital Los Angeles, Los Angeles, California, United States

    Contact: Study coordinator (Lee Chen) · lchen@chla.usc.edu · 323-361-5812
    Contact: Principal Investigator (Alan Wayne)
  • UCLA Medical Center, Los Angeles, California, United States

    Study coordinator · 310-825-4493
    Contact: Principal Investigator (Aravind Ramakrishnan)
  • UCSF Medical Center, San Francisco, California, United States

    Contact: Study coordinator (Jenai Wilmoth) · jenai.wilmoth@ucsf.edu · 415-514-6281
    Contact: Principal Investigator (Charalambos Andreadis)
  • Stanford University Medical Center, Stanford, California, United States

    Contact: Study coordinator (Christina Baggott) · Baggott@stanford.edu · 650-723-4000
    Contact: Principal Investigator (Kara Davis)
  • Emory University School of Medicine-Winship Cancer Institute, Atlanta, Georgia, United States

    Contact: Study coordinator (Sharah Triplett) · Sharra.triplett@emory.edu
    Contact: Principal Investigator (Jonathon Cohen)
  • Emory University School of Medicine/Winship Cancer Institute, Atlanta, Georgia, United States

    Contact: Study coordinator (Keshawna L. Sherer) · keshawna.sherer@emoryhealthcare.org · 404-778-3708
    Contact: Principal Investigator (Jonathon Cohen)
  • Childrens Healthcare of Atlanta, Atlanta, Georgia, United States

    Contact: Study coordinator (Audry Grizzle Tumlin) · audrey.tumlin@choa.org · +1 404 785 2125
    Contact: Principal Investigator (Muna Qayed)
  • Uni of Chi Medi Ctr Hema and Onco, Chicago, Illinois, United States

    Contact: Study coordinator (Linda Schroeder) · lschroed@medicine.bsd.uchicago.edu · 773-834-0982
    Contact: Principal Investigator (Michael R Bishop)
  • University of Chicago Medical Center, Hematology & Oncology, Chicago, Illinois, United States

    Contact: Study coordinator (Howie Weiner) · hweiner@medicine.bsd.uchicago.edu · 773-834-0982
    Contact: Principal Investigator (Michael R. Bishop)
  • University of Kansas Cancer Center SC, Westwood, Kansas, United States

    Contact: Study coordinator (Janie Smart) · nsmart@kumc.edu · 913-588-6029
    Contact: Principal Investigator (Joseph P McGuirk)
  • University of Kansas Cancer Center, Westwood, Kansas, United States

    Contact: Study coordinator (Maghen Farris) · mfarris@kumc.edu · 913-588-6029
    Contact: Principal Investigator (Joseph P McGuirk)
  • Massachusetts General Hospital, Boston, Massachusetts, United States

    Contact: Principal Investigator (Matthew Frigault)
  • Beth Israel Deaconess Med Center, Boston, Massachusetts, United States

    Study coordinator · 617-667-7000
    Contact: Principal Investigator (Jacalyn Rosenblatt)
  • Dana Farber Cancer Institute, Boston, Massachusetts, United States

    Study coordinator · 617-632-3985
    Contact: Principal Investigator (Adam Sperling)
  • University of Michigan, Ann Arbor, Michigan, United States

    Contact: Study coordinator (Sabrina Hargrove) · sgomes@med.umich.edu
    Contact: Principal Investigator (Gregory Yanik)
  • Uni Of Michigan Health System, Ann Arbor, Michigan, United States

    Contact: Study coordinator (Sabrina Hargrove) · sgomes@med.umich.edu · 734-936-8538
    Contact: Principal Investigator (John Magenau)
  • University of Michigan Health System SC CTL019, Ann Arbor, Michigan, United States

    Contact: Study coordinator (Michelle Smith Tucker) · smimiche@umich.edu · 734-936-8538
    Contact: Principal Investigator (John Magenau)
  • Wayne State University-Karmanos Cancer Institute, Detroit, Michigan, United States

    Study coordinator · 313-576-8716
    Contact: Principal Investigator (Abhinav Deol)
  • University of Minnesota, Minneapolis, Minnesota, United States

  • Children s Mercy Hospital, Kansas City, Missouri, United States

    Contact: Study coordinator (Allison Miles) · almiles1@cmh.edu · 816-855-1886
    Contact: Principal Investigator (Gary D. Myers)
  • Children's Mercy Hospital SC, Kansas City, Missouri, United States

    Contact: Study coordinator (Rachel Wilcox) · rwilcox@cmh.edu · 816-302-6851
    Contact: Principal Investigator (Gary Myers, MD)
    Contact: Principal Investigator (Gary D. Myers)
  • Weill Cornell Medical College, New York, New York, United States

  • Duke Unversity Medical Center SC - CTL019B2205J, Durham, North Carolina, United States

    Contact: Study coordinator (Kristine Edwards) · kristine.gurganus@dm.duke.edu · 919-668-2967
    Contact: Study coordinator (Erin Arbuckle) · erin.arbuckle@duke.edu · 919-684-3293
    Contact: Principal Investigator (Paul L. Martin)
  • Duke Unversity Medical Center, Durham, North Carolina, United States

    Contact: Study coordinator (Nelson Chao) · nelson.chao@duke.edu
    Contact: Principal Investigator (Paul L. Martin)
  • Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United States

    Contact: Study coordinator (Melanie Jordan) · melanie.jordan@cchmc.org · 513-636-9292
    Contact: Principal Investigator (Stella M. Davies)
  • Cinn Children Hosp Medical Center, Cincinnati, Ohio, United States

    Contact: Study coordinator (Kristie Evans Stricker) · kristie.stricker@chmc.org · +1 513 636 9292
    Contact: Principal Investigator (Stella M. Davies)
  • Ohio ST Compr Cancer Ctr James Hosp, Columbus, Ohio, United States

    Contact: Study coordinator (Molly Vittorio) · Molly.Vittorio@osumc.edu · 614-688-9494
    Contact: Principal Investigator (David A Bond)
  • Oregon Health & Science University, Portland, Oregon, United States

    Contact: Study coordinator (Beth Zentzis) · zentzis@ohsu.edu · 503-346-1507
    Contact: Principal Investigator (Brandon Hayes-Lattin)
  • Oregon Health Sciences University, Portland, Oregon, United States

    Contact: Study coordinator (Mai-Lee Lee Yap) · yap@ohsu.edu · +1 503 494 6865
    Contact: Principal Investigator (Brandon Hayes-Lattin)
  • The Childrens Hosp of Philadelphia, Philadelphia, Pennsylvania, United States

    Contact: Study coordinator (Lauren Vernau) · VERNAUL@EMAIL.CHOP.EDU · 215-590-7399
    Contact: Principal Investigator (Stephan Grupp)
  • University of Pennsylvania, Philadelphia, Pennsylvania, United States

    Contact: Study coordinator (Michelle Caylor) · mcaylor@mail.med.upenn.edu · 215-898-9256
    Contact: Principal Investigator (Noelle Frey)
  • University of Pennsylvania, Philadelphia, Pennsylvania, United States

    Contact: Study coordinator (Desire Fenderson) · dfend@upenn.edu · 215-615-1725
    Contact: Principal Investigator (Noelle Frey)
  • Thomas Jefferson University, Philadelphia, Pennsylvania, United States

    Study coordinator · 215-955-8699
    Contact: Principal Investigator (Usama Gergis)
  • Sarah Cannon Research Institute, Nashville, Tennessee, United States

    Contact: Principal Investigator (Ian W Flinn)
  • UTSW/Children's Medical Center, Dallas, Texas, United States

    Contact: Study coordinator (Alison Patterson) · Alison.patterson@childrens.com · 214-456-2726
    Contact: Principal Investigator (Theodore Laetsch, MD)
    Contact: Principal Investigator (Theodore Laetsch)
  • University of Texas Southwestern Medical Center, Dallas, Texas, United States

    Contact: Study coordinator (Cris Molina) · cris.molina@childrens.com · 214-648-6449
    Contact: Principal Investigator (Samuel John)
  • MD Anderson Cancer Center SC, Houston, Texas, United States

    Contact: Study coordinator (Souzanne T. Ouzounian) · souzouni@mdanderson.org · 713-792-2171
    Contact: Study coordinator (Laura Hargraves) · lehargraves@mdanderson.org · 713-792-6594
    Contact: Principal Investigator (Jason Westin)
  • MD Anderson Cancer Center, Houston, Texas, United States

    Contact: Study coordinator (Souzanne T Ouzounian) · souzouni@mdanderson.org · 713-792-2171
    Contact: Principal Investigator (Jason Westin)
  • University of Utah Clinical Trials Office, Salt Lake City, Utah, United States

    Contact: Study coordinator (Luke Stone) · luke.stone@hsc.utah.edu · 801-213-3395
    Contact: Principal Investigator (Michael Boyer, MD)
    Contact: Principal Investigator (Michael Boyer)
  • University of Utah Clinical Trials Office, Salt Lake City, Utah, United States

    Contact: Study coordinator (Sydney Goosen) · Sydney.Goosen@hsc.utah.edu · 801-213-3401
    Contact: Principal Investigator (Michael Pulsipher)
  • University of Wisconsin Hospital and Clinics, Madison, Wisconsin, United States

    Contact: Study coordinator (Jenny Weiland) · PedsHemOncResearch@lists.wisc.edu · 608-890-8070
    Contact: Study coordinator (Celeste Matsushima) · camatsus@pediatrics.wisc.edu · +1 608-890-8069
    Contact: Principal Investigator (Christian Capitini)
  • University of Wisconsin Hospital, Madison, Wisconsin, United States

    Contact: Study coordinator (Kreg M Grindle) · kgrindle@uwhealth.org
    Contact: Principal Investigator (Christian Capitini)
  • Novartis Investigative Site, Camperdown, New South Wales, Australia

  • Novartis Investigative Site, Melbourne, Victoria, Australia

  • Novartis Investigative Site, Melbourne, Victoria, Australia

  • Novartis Investigative Site, Parkville, Victoria, Australia

  • Novartis Investigative Site, Murdoch, Western Australia, Australia

  • Novartis Investigative Site, Herston, Australia

  • Novartis Investigative Site, Linz, Austria

  • Novartis Investigative Site, Salzburg, Austria

  • Novartis Investigative Site, Vienna, Austria

  • Novartis Investigative Site, Vienna, Austria

  • Novartis Investigative Site, Ghent, Belgium

  • Novartis Investigative Site, Hamilton, Ontario, Canada

  • Novartis Investigative Site, Toronto, Ontario, Canada

  • Novartis Investigative Site, Montreal, Quebec, Canada

  • Novartis Investigative Site, Montreal, Quebec, Canada

  • Novartis Investigative Site, Beijing, China

  • Novartis Investigative Site, Copenhagen, Denmark

  • Novartis Investigative Site, Helsinki, Finland

  • Novartis Investigative Site, Nantes, France

  • Novartis Investigative Site, Paris, France

  • Novartis Investigative Site, Paris, France

  • Novartis Investigative Site, Pierre-Bénite, France

  • Novartis Investigative Site, Villejuif, France

  • Novartis Investigative Site, Munich, Bavaria, Germany

  • Novartis Investigative Site, Regensburg, Bavaria, Germany

  • Novartis Investigative Site, Würzburg, Bavaria, Germany

  • Novartis Investigative Site, Frankfurt am Main, Hesse, Germany

  • Novartis Investigative Site, Cologne, North Rhine-Westphalia, Germany

  • Novartis Investigative Site, Leipzig, Saxony, Germany

  • Novartis Investigative Site, Berlin, Germany

  • Novartis Investigative Site, Hamburg, Germany

  • Novartis Investigative Site, Ulm, Germany

  • Novartis Investigative Site, Chaïdári, Greece

  • Novartis Investigative Site, Hong Kong, Hong Kong

  • Novartis Investigative Site, Ramat Gan, Israel

  • Novartis Investigative Site, Tel Aviv, Israel

  • Novartis Investigative Site, Bologna, BO, Italy

  • Novartis Investigative Site, Monza, MB, Italy

  • Novartis Investigative Site, Milan, MI, Italy

  • Novartis Investigative Site, Milan, MI, Italy

  • Novartis Investigative Site, Rozzano, MI, Italy

  • Novartis Investigative Site, Roma, RM, Italy

  • Novartis Investigative Site, Roma, RM, Italy

  • Novartis Investigative Site, Fukuoka, Fukuoka, Japan

  • Novartis Investigative Site, Sapporo, Hokkaido, Japan

  • Novartis Investigative Site, Sendai, Miyagi, Japan

  • Novartis Investigative Site, Chuo Ku, Tokyo, Japan

  • Novartis Investigative Site, Kyoto, Japan

  • Novartis Investigative Site, Amsterdam, North Holland, Netherlands

  • Novartis Investigative Site, Utrecht, Netherlands

  • Novartis Investigative Site, Utrecht, Netherlands

  • Novartis Investigative Site, Oslo, Norway

  • Novartis Investigative Site, Oslo, Norway

  • Novartis Investigative Site, Riyadh, Saudi Arabia

  • 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, Seoul, South Korea

  • Novartis Investigative Site, Seoul, South Korea

  • Novartis Investigative Site, Esplugues, Barcelona, Spain

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

  • Novartis Investigative Site, Salamanca, Castille and León, Spain

  • Novartis Investigative Site, Barcelona, Catalonia, Spain

  • Novartis Investigative Site, Pamplona, Navarre, Spain

  • Novartis Investigative Site, Barcelona, Spain

  • Novartis Investigative Site, Madrid, Spain

  • Novartis Investigative Site, Madrid, Spain

  • Novartis Investigative Site, Madrid, Spain

  • Novartis Investigative Site, Seville, Spain

  • Novartis Investigative Site, Valencia, Spain

  • Novartis Investigative Site, Taipei, Taiwan

  • Novartis Investigative Site, Birmingham, United Kingdom

  • Novartis Investigative Site, London, United Kingdom

Study leads
  • Novartis Pharmaceuticals

    Study Director

    Novartis Pharmaceuticals