Advanced Solid Cancer
Conditions
Brief summary
The study is being conducted to assess the safety and tolerability of SHR-A1904 in patients with advanced solid cancer and to determine the dose-limiting toxicity (DLT), maximum tolerated dose (MTD), and recommended phase II dose (RP2D) of SHR-A1904
Interventions
DRUGSHR-A1904
SHR-A1904
Sponsors
Shanghai Hengrui Pharmaceutical Co., Ltd.
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
SHR-A1904 monotherapy
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
1. Evidence of a personally signed and dated informed consent document indicating that the subject has been informed of all pertinent aspects of the study 2. Males or females aged 18-75 years old 3. Eastern Cooperative Oncology Group (ECOG) performance status of 0-1 4. Has a life expectancy≥ 3 months 5. Has at least one measurable lesion as defined by RECIST v1.1 6. Pathologically confirmed advanced solid cancer
Exclusion criteria
1. Plan to receive any other anti-tumor treatments during the study treatment period of this study 2. Received other clinical investigational products or treatments within 4 weeks before the first dose of the study 3. Received anti-tumor therapies such as chemotherapy, radiotherapy, biological therapy, targeted therapy, or immunotherapy within 4 weeks before the first dose of the study 4. Underwent a major surgery other than diagnosis or biopsy within 4 weeks before the first dose of the study 5. Subjects with known brain metastases 6. Grade II-IV cardiac insufficiency as per the New York Heart Association (NYHA) criteria; arrhythmia requiring long-term drug control; unstable angina or acute myocardial infarction within 6 months before the first dose of the study 7. presence of accompanying diseases (such as poorly controlled hypertension, serious diabetes mellitus, thyroid disorder, psychosis, etc.) that may pose serious risks to the safety of the subject or may affect the subject's ability to complete the study, or any other situation as judged by the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Determine the Maximum Tolerated Dose of SHR-A1904 | up to 1 year |
Secondary
| Measure | Time frame |
|---|---|
| Maximum concentration (Cmax) | up to 1 year |
| Time to maximum concentration (Tmax) | up to 1 year |
| Area under the drug concentration-time curve from time 0 to the last measurable concentration time point (AUC0-t) | up to 1 year |
| Anti-drug antibody (ADA) of SHR-A1904 | up to 1 year |
| Objective response rate (ORR) | up to 1 year |
Countries
China
Outcome results
None listed