A Study of LY4584180 in Adult Participants With Previously Treated Blood Cancers
Sponsor: Eli Lilly and Company • ClinicalTrials.gov ID: NCT07226843
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The main purpose of this study is to evaluate safety and efficacy, and measure how much LY4584180 gets into the bloodstream and how long it takes the body to eliminate it in patients with previously treated blood cancers. For each participant, the study could last about 9 months or possibly longer including screening.
Interventions
-
LY4584180
(Drug)
administered orally
-
Rituximab
(Drug)
administered through IV infusion
Eligibility criteria
Conditions
Locations
- Mayo Clinic - Scottsdale — Scottsdale, Arizona, United States
- City of Hope — Duarte, California, United States
- University of California, Los Angeles (UCLA) - Medical Center — Los Angeles, California, United States
- University of California, San Francisco (UCSF) - Helen Diller Family Comprehensive Cancer Center — San Francisco, California, United States
- Colorado Blood Cancer Institute — Denver, Colorado, United States
- University of Miami - Sylvester Cancer Center — Miami, Florida, United States
- Florida Cancer Specialists - Sarasota — Sarasota, Florida, United States
- Emory University Hospital — Atlanta, Georgia, United States
- Massachusetts General Hospital — Boston, Massachusetts, United States
- Dana-Farber Cancer Institute — Boston, Massachusetts, United States
- Mayo Clinic - Rochester — Rochester, Minnesota, United States
- Columbia University — New York, New York, United States
- University of Rochester — Rochester, New York, United States
- The Ohio State University (OSU) — Columbus, Ohio, United States
- Oregon Health & Science University (OHSU) — Portland, Oregon, United States
- Sarah Cannon Research Institute — Nashville, Tennessee, United States
- Vanderbilt University Medical Center — Nashville, Tennessee, United States
- Texas Oncology - DFW (Sammons CC) — Dallas, Texas, United States
- Baylor College of Medicine — Houston, Texas, United States
- University of Washington - Fred Hutchinson Cancer Center (Seattle Cancer Care Alliance) — Seattle, Washington, United States
- Froedtert Hospital and the Medical College of Wisconsin — Milwaukee, Wisconsin, United States
- CHU de Nantes - Hotel-Dieu — Nantes, France
- Institut Curie — Paris, France
- CHU Bordeaux - Hopital Haut-Leveque - Centre Francois Magendie — Pessac, France
- HCL Centre Hospitalier Lyon Sud — Pierre-Bénite, France
- Oncopole Claudius Regaud — Toulouse, France
- Charite Universitaetsmedizin Berlin — Berlin, Germany
- Universitaetsklinikum Koeln (AoeR) — Cologne, Germany
- Universitaetsklinikum Essen — Essen, Germany
- Universitaetsklinikum Frankfurt - Klinikum der Johann Wolfgang Goethe Universitaet — Frankfurt am Main, Germany
- IRCCS Azienda Ospedaliero-Universitaria di Bologna - Policlinico di Sant Orsola — Bologna, Italy
- Istituto Europeo di Oncologia — Milan, Italy
- National Cancer Center Hospital East — Chiba, Japan
- Okayama University Hospital — Okayama, Japan
- Cancer Institute Hospital of JFCR — Tokyo, Japan
- Pratia Onkologia Katowice — Katowice, Poland
- Pratia MCM Krakow — Krakow, Poland
- AIDPORT Sp. z o.o. — Skorzewo, Poland
- Instytut Hematologii i Transfuzjologii w Warszawie — Warsaw, Poland
- Institut Catala d'Oncologia - L'Hospitalet — Barcelona, Spain
- South Texas Accelerated Research Therapeutics (START) Madrid - Hospital Fundacion Jimenez Diaz — Madrid, Spain
- King's College Hospital — London, United Kingdom
- The Royal Marsden NHS Foundation Trust — London, United Kingdom
- Nottingham City Hospital — Nottingham, United Kingdom
- Derriford Hospital — Plymouth, United Kingdom
- University Hospital Southampton NHS Foundation Trust — Southampton, United Kingdom
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Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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