Overview

A Study of SHR-A1811 in Subjects With Advanced Malignant Solid Tumors

Status:
Recruiting
Trial end date:
2023-12-01
Target enrollment:
0
Participant gender:
All
Summary
This is an open-label, two-part study to evaluate the safety, tolerability, pharmacokinetics and immunogenicity of SHR-A1811 and preliminary anti-tumor efficacy in HER2 expressing or mutated advanced malignant solid tumor subjects.
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Jiangsu HengRui Medicine Co., Ltd.
Collaborator:
Atridia Pty Ltd.
Criteria
Inclusion Criteria:

- Advanced/unresectable or metastatic solid tumor with HER2 expression or mutation that
is refractory to or intolerable with standard treatment, or for which no standard
treatment is available

- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1

- LVEF ≥ 50% by either ECHO or MUGA

- Has adequate renal and hepatic function

- Female subjects agree not to be pregnant or lactating from beginning of the study
screening until 6 months after receiving the last treatment

Exclusion Criteria:

- History of clinically significant lung diseases (e.g., interstitial pneumonia,
pneumonitis, pulmonary fibrosis, and severe radiation pneumonitis) or suspected to
have these diseases by imaging at screening period

- Known hereditary or acquired bleeding and thrombotic tendency