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Spots Global Cancer Trial Database for A Study of LOXO-435 in Participants With Cancer With a Change in a Gene Called FGFR3

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Trial Identification

Brief Title: A Study of LOXO-435 in Participants With Cancer With a Change in a Gene Called FGFR3

Official Title: An Open-Label, Multicenter Study of LOXO-435 (LY3866288) In Advanced Solid Tumor Malignancies With FGFR3 Alterations

Study ID: NCT05614739

Study Description

Brief Summary: The main purpose of this study is to learn more about the safety, side effects, and effectiveness of LOXO-435. LOXO-435 may be used to treat cancer of the cells that line the urinary system and other solid tumor cancers that have a change in a particular gene (known as the FGFR3 gene). Participation could last up to 30 months (2.5 years) and possibly longer if the disease does not get worse.

Detailed Description: This is an open-label, multi-center, phase 1a/b study in participants with FGFR3-altered advanced solid tumors, including metastatic urothelial cancer (UC). The study will be conducted in 2 phases: Dose escalation and dose optimization (1a) and dose expansion (1b). Phase 1a will include up to 2 cohorts to assess safety, tolerability, and pharmacokinetics of LOXO-435 to determine the recommended phase 2 dose (RP2D) (or optimal dose). Phase 1b will include 4 dose expansion cohorts of participants with prespecified activating FGFR3 alterations to evaluate the efficacy and safety of LOXO-435 at the RP2D. Cohort B will enroll pts with metastatic UC and includes three cohorts to evaluate LOXO-435 as monotherapy (B1, B2) and in combination with pembrolizumab (B3). Cohort C will enroll pts with non-UC advanced solid tumors and includes a cohort to evaluate LOXO-435 as monotherapy (C1).

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

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

UCLA Department of Medicine-Hematology/Oncology, Santa Monica, California, United States

Advent Health Hematology and Oncology, Celebration, Florida, United States

Winship Cancer Institute, Emory University, Atlanta, Georgia, United States

The University of Chicago Medical Center, Chicago, Illinois, United States

SKCCC at Johns Hopkins, Baltimore, Maryland, United States

Massachusetts General Hospital, Boston, Massachusetts, United States

Karmanos Cancer Institute, Detroit, Michigan, United States

Washington University School of Medicine, Saint Louis, Missouri, United States

Laura and Isaac Perlmutter Cancer Center, New York, New York, United States

Icahn School of Medicine at Mount Sinai, 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

University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, United States

Penn Medicine: University of Pennsylvania Health System/Perelman Center for Advanced Medicine, Philadelphia, Pennsylvania, United States

University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States

Carolina Urologic Research Center, Myrtle Beach, South Carolina, United States

Tennessee Oncology PLLC, Nashville, Tennessee, United States

University of Texas Southwestern Medical Center, Dallas, Texas, United States

MD Anderson Cancer Center, Houston, Texas, United States

Huntsman Cancer Institute, Salt Lake City, Utah, United States

Royal North Shore Hospital, Saint Leonards, New South Wales, Australia

Kinghorn Cancer Centre, Darlinghurst, , Australia

British Columbia Cancer Agency, Vancouver, British Columbia, Canada

Princess Margaret Hospital, Toronto, Ontario, Canada

Beijing Cancer hospital, Beijing, Beijing, China

Beijing Cancer hospital, Haidian, Beijing, China

Sun Yat-sen University Cancer Center, Guangzhou, Guangdong, China

Renji Hospital Affliated to Shanghai Jiaotong University, Shanghai, Shanghai, China

The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shanxi, China

Zhejiang Provincial People's Hospital, Hangzhou, Zhejiang, China

Zhejiang University, Hangzhou, Zhejiang, China

Tianjin Medical University Cancer Institute & Hospital, Tianjin, Zhejiang, China

Institut Bergonié - Centre Régional de Lutte Contre Le Cancer de Bordeaux et Sud Ouest, Bordeaux, Aquitaine, France

Gustave Roussy, Villejuif, Shanxi, France

Centre Leon Berard, Lyon, , France

Klinikum rechts der Isar de Technischen Universitaet Muenchen, München, , Germany

Universitaetsklinikum Tuebingen, Tuebingen, , Germany

Beilinson Hospital, Petach Tikva, HaMerkaz, Israel

Sheba Medical Center, Ramat Gan, HaMerkaz, Israel

IRCCS Ospedale San Raffaele, Milano, Milan, Italy

UOC Fase I - Fondazione Policlinico Universitario A. Gemelli IRCCS - Universita Cattolica del Sacro Cuore, Roma, , Italy

Aichi Cancer Center Hospital, Nagoya, Aichi, Japan

National Cancer Center Hospital, Chuo Ku, Tokyo, Japan

National Cancer Center Hospital East, Chiba, , Japan

The Cancer Institute Hospital of JFCR, Tokyo, , Japan

Asan Medical Center, Seoul, Seoul], Korea, Republic of

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

Severance Hospital, Yonsei University Health System, Seoul, , Korea, Republic of

Samsung Medical Center, Seoul, , Korea, Republic of

Erasmus Medisch Centrum, Rotterdam, Zuid-Holland, Netherlands

Oslo University Hospital Ullevaal, Oslo, Roma, Norway

Haukeland University, Bergen, , Norway

Institut Catala d'Oncologia L'Hospitalet, Barcelona, , Spain

Centro Oncológico MD Anderson, Madrid, , Spain

Hospital Universitario 12 de Octubre, Madrid, , Spain

South Texas Accelerated Research Therapeutics (START) Madrid, Madrid, , Spain

Hospital Universitario Marques de Valdecilla, Santander, , Spain

The Christie NHS Foundation Trust, Manchester, , United Kingdom

Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, , United Kingdom

Contact Details

Name: Ryan Widau, PhD

Affiliation: Loxo Oncology, Inc.

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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