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Spots Global Cancer Trial Database for A Study of Oral LOXO-305 in Patients With Previously Treated CLL/SLL or NHL

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Trial Identification

Brief Title: A Study of Oral LOXO-305 in Patients With Previously Treated CLL/SLL or NHL

Official Title: A Phase 1/2 Study of Oral LOXO-305 in Patients With Previously Treated Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma (CLL/SLL) or Non-Hodgkin Lymphoma (NHL)

Study ID: NCT03740529

Study Description

Brief Summary: This is an open-label, multi-center Phase 1/2 study of oral LOXO-305 (pirtobrutinib) in patients with CLL/SLL and NHL who have failed or are intolerant to standard of care.

Detailed Description: This study includes 3 parts: Phase 1 (pirtobrutinib monotherapy dose escalation and dose expansion), Phase 1b (pirtobrutinib combination therapy dose expansion), and Phase 2 (pirtobrutinib monotherapy dose expansion). In Phase 1, patients will be enrolled using an accelerated titration design. The starting dose of pirtobrutinib in oral tablet form is 25 mg/day (e.g., 25 mg once daily \[QD\]). Once the MTD and/or RP2D is identified in Phase 1 dose escalation, enrollment will continue to Phase 1 dose expansion and can commence to Phase 1b (Arms A and B). For Phase 2, patients will be enrolled to one of seven Phase 2 dose expansion cohorts depending on tumor histology and prior treatment history. Cycle length will be 28 days.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Mayo Clinic of Scottsdale, Scottsdale, Arizona, United States

Scripps Coastal Medical Center, San Diego, California, United States

University of California San Francisco, Medical Center at Paranassus, San Francisco, California, United States

Smilow Cancer Hospital at Yale-New Haven, New Haven, Connecticut, United States

Mayo Clinic-Jacksonville, Jacksonville, Florida, United States

Florida Cancer Specialists ORLANDO/DDU, Lake Mary, Florida, United States

Sylvester Comprehensive Cancer Center, Miami, Florida, United States

Florida Cancer Specialists, Sarasota, Florida, United States

Emory Clinic, Atlanta, Georgia, United States

Northwestern University, Chicago, Illinois, United States

University of Kansas Medical Center, Kansas City, Kansas, United States

Dana-Farber Cancer Institute, Boston, Massachusetts, United States

Mayo Clinic, Rochester, Minnesota, United States

University of Nebraska Medical Center, Omaha, Nebraska, United States

Roswell Park Cancer Institute, Buffalo, New York, United States

Northwell Health, New Hyde Park, New York, United States

Columbia University Medical Center, New York, New York, United States

Memorial Sloan Kettering Cancer Center, New York, New York, United States

University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States

Durham VA Medical Center, Durham, North Carolina, United States

Duke University Medical Center, Durham, North Carolina, United States

Cleveland Clinic Foundation, Cleveland, Ohio, United States

Ohio State University Hospital, Columbus, Ohio, United States

University of Pennsylvania Hospital, Philadelphia, Pennsylvania, United States

Sarah Cannon Research Institute SCRI, Nashville, Tennessee, United States

Mary Crowley Cancer Research Center, Dallas, Texas, United States

University of Texas MD Anderson Cancer Center, Houston, Texas, United States

Utah Cancer Specialists, Salt Lake City, Utah, United States

Swedish Medical Center, Seattle, Washington, United States

Seattle Cancer Care Alliance, Seattle, Washington, United States

Medical College of Wisconsin, Milwaukee, Wisconsin, United States

Flinders Medical Centre, Bedford Park, South Australia, Australia

Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia

Linear Clinical Research, Nedlands, Western Australia, Australia

Centre Hospitalier Universitaire de Nantes - L' Hopital l'hôtel-Dieu, Nantes Cedex 1, , France

IRCCS - AOU di Bologna, Bologna, , Italy

IRCCS Ospedale San Raffaele, Milano, , Italy

Nagoya Medical Center, Nagoya, Aichi, Japan

Hokkaido University Hospital, Sapporo, Hokkaido, Japan

Tokai University Hospital- Isehara Campus, Isehara, Kanagawa, Japan

Kochi Medical School Hospital, Nankoku, Kochi, Japan

Tohoku University Hospital, Sendai, Miyagi, Japan

National Cancer Center Hospital, Chuo Ku, Tokyo, Japan

National Hospital Organization Kyushu Cancer Center, Fukuoka, , Japan

Kyoto Furitsu Medical University Hospital, Kyoto, , Japan

Okayama University Hospital, Okayama, , Japan

Kindai University Hospital, Osakasayama-Shi, , Japan

Samsung Medical Center, Seoul, Seoul-teukbyeolsi [Seoul], Korea, Republic of

Seoul National University Hospital, Seoul, , Korea, Republic of

Pratia MCM Krakow, Krakow, , Poland

Instytut Hermatologii I Transfuzjologii, Warszawa, , Poland

Karolinska Institutet, Solna, AB, Sweden

Ospedale Regionale Bellinzona e Valli, Bellinzona, Ticino, Switzerland

St James's University Hospital, Leeds, , United Kingdom

Churchill Hospital, Oxford, , United Kingdom

Derriford Hospital, Plymouth, , United Kingdom

Contact Details

Name: Donald Tsai, MD, PhD

Affiliation: Loxo Oncology

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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