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Brief Title: A Study of IMC-002 in Patients With Advanced Cancer Failed to Standard Therapy
Official Title: An Open-Label, Dose-Escalation and Expansion, Phase I Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Clinical Activity of IMC-002 in Patients With Advanced Cancer Failed to Standard Therapy
Study ID: NCT05276310
Brief Summary: This is an Open-Label, Dose-Escalation and Expansion, Phase I Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Clinical Activity of IMC-002 in Patients with Advanced Cancer Failed to Standard Therapy
Detailed Description: The purpose of this study is to evaluate safety and tolerability and to determine the maximum tolerated dose (MTD) and the recommended phase 2 dose (RP2D) of IMC-002. Multiple-dose levels of IMC-002 will be tested in subjects with advanced cancer.
Minimum Age: 19 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Asan Medical Center, Republic of Korea, Seoul, , Korea, Republic of
Samsung Medical Center, Seoul, , Korea, Republic of
Name: HEUNG TAE KIM, MD
Affiliation: ImmuneOncia Therapeutics Inc.
Role: STUDY_DIRECTOR