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Brief Title: A Study of HMPL-415S1 in Patients With Advanced Malignant Solid Tumors
Official Title: A Multicenter, Open-Label Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of HMPL-415S1 in Patients With Advanced Malignant Solid Tumor
Study ID: NCT05886374
Brief Summary: The objective of this study is to evaluate the safety, tolerability and PK profile of HMPL-415S1 and determine MTD and/or RP2D in patients with advanced malignant solid tumor.
Detailed Description: This study is expected to enroll 36-81 patients, including 26-66 patients for dose escalation, additional 10-15 patients will be enrolled at the dose level of determined RP2D.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Zhongshan Hospital Fudan University, Shanghai, Shanghai, China
Name: Bin Yang
Affiliation: Hutchison Medipharma Limited
Role: STUDY_DIRECTOR