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First in Human Study of TORL-1-23 in Participants With Advanced Cancer
Sponsor: TORL Biotherapeutics, LLC
Summary
This first-in-human study will evaluate the safety, tolerability, pharmacokinetics, and antitumor activity of TORL-1-23 in patients with advanced cancer
Official title: A Phase 1, First in Human, Dose-Escalation Study of TORL-1-23 in Participants With Advanced Cancer
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
90
Start Date
2021-11-17
Completion Date
2026-11-15
Last Updated
2026-02-13
Healthy Volunteers
No
Interventions
TORL-1-23
antibody drug conjugate (ADC)
Locations (14)
Providence Medical Foundation
Fullerton, California, United States
UCLA - JCCC Clinical Research Unit
Los Angeles, California, United States
University of Kentucky Medical Center
Lexington, Kentucky, United States
University of Minnesota
Minneapolis, Minnesota, United States
Mayo Clinic in Rochester
Rochester, Minnesota, United States
Memorial Sloan Kettering Cancer Center
New York, New York, United States
Cleveland Clinic
Cleveland, Ohio, United States
Sarah Cannon Research Institute Texas Oncology
Tyler, Texas, United States
Virginia Cancer Specialists
Fairfax, Virginia, United States
St. Vincent's Hospital, The Catholic University of Korea
Suwon, Gyeonggi-do, South Korea
Seoul National University Hospital
Seoul, South Korea
Severance Hospital
Seoul, South Korea
Asan Medical Center
Seoul, South Korea
Samsung Medical Center
Seoul, South Korea