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Brief Title: A Study of MRG002 in the Treatment of Patients With HER2-positive Advanced Solid Tumors
Official Title: A Phase I, Open-label, Multi-center, First in Human, Dose Escalation and Expansion Study to Assess the Safety, Tolerability, Efficacy and Pharmacokinetics of MRG002 in Patients With HER2 Positive Advanced Solid Tumors
Study ID: NCT04941339
Brief Summary: The objective of this study is to assess the safety, efficacy, pharmacokinetics, and immunogenicity of MRG002 in patients with HER2-positive advanced solid tumors.
Detailed Description: This study consists of two parts. Phase Ia is a dose escalation study to determine the maximum tolerated dose (MTD) and recommended phase II dose (RP2D) of MRG002. Phase Ib is a dose expansion study to further assess the efficacy and safety of MRG002 at confirmed RP2D.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Shanghai Oriental Hospital, Shanghai, Shanghai, China
Name: Jin Li, Doctor
Affiliation: Shanghai Oriental Hospital
Role: PRINCIPAL_INVESTIGATOR