ARTEMIS-006: HS-20093 in Patients With Head and Neck Squamous Cell Carcinoma and Other Solid Tumors

Launched by HANSOH BIOMEDICAL R&D COMPANY · Aug 17, 2023

Keywords

ClinConnect Summary

The ARTEMIS-006 clinical trial is studying a new treatment called HS-20093 for patients with head and neck squamous cell carcinoma, which is a type of cancer that affects the throat and mouth, as well as other solid tumors. HS-20093 is a special type of medicine that targets specific proteins found on cancer cells to help fight the disease. This trial aims to find out how well HS-20093 works, how safe it is, and how the body processes it.

To be eligible for this trial, participants must be at least 18 years old, have been treated for their cancer but have not had success with standard therapies, and have at least one measurable tumor. Patients will be closely monitored throughout the study, and they will need to provide certain samples, like tumor tissue, to help researchers understand the treatment's effects. The trial is currently recruiting participants of all genders, and it offers an opportunity for those who may not have many treatment options left to contribute to important research.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • 1. At least age of 18 years at screening. 2. Patients，who have progressed on or intolerant to standard therapie，with histologically confirmed recurrent/metastatic HNSCC or other solid tumor.
• • 3. At least one measurable lesion according to RECIST 1.1. 4. Agree to provide fresh or archival tumor tissue and peripheral blood samples.
• • 5. Eastern Cooperative Oncology Group (ECOG) Performance Status of 0\~1. 6. Life expectancy \>= 12 weeks. 7. Men or women should be using adequate contraceptive measures throughout the study.
• • 8. Female subjects must not be pregnant at screening or have evidence of non-childbearing potential.
• • 9. Signed and dated Informed Consent Form.
• Exclusion Criteria:
• * 1. Treatment with any of the following:
• • 1. Previous or current treatment with B7-H3 targeted therapy
• • 2. Any cytotoxic chemotherapy, investigational agents and small molecule targeted therapy within 14 days prior to the first scheduled dose of HS-20093
• • 3. Prior treatment with macromolecule anti-tumor therapy or other anticancer drugs within 28 days prior to the first scheduled dose of HS-20093
• • 4. Radiotherapy with a limited field of radiation for palliation within 2 weeks, or patients received more than 30% of the bone marrow irradiation, or large-scale radiotherapy within 4 weeks prior to the first scheduled dose of HS-20093
• • 5. Pleural or peritoneal effusion requiring clinical intervention. Pericardial effusion
• • 6. Major surgery within 4 weeks of the first dose of HS-20093
• • 7. Spinal cord compression or brain metastases.
• • 8. Treatment with drugs that are predominantly CYP3A4 strong inhibitors or inducers or sensitive substrates of CYP3A4 with a narrow therapeutic range within 7 days of the first dose of study drug; or requiring treatment with these drugs during the study.
• • 9. Currently receiving drugs known to prolong QT interval or may cause torsade de pointe; or requiring treatment with these drugs during the study.
• • 2. Any unresolved toxicities from prior therapy greater than Grade 2 according to Common Terminology Criteria for Adverse Events (CTCAE) 5.0 with the exception of stable hypothyroidism treated with hormone replacement therapy, alopecia or neurotoxicity.
• • 3. History of other primary malignancies. 4. Inadequate bone marrow reserve or organ dysfunction 5. Evidence of cardiovascular risk. 6. Severe, uncontrolled or active cardiovascular diseases. 7. Diabetes ketoacidosis or hyperglycemia hypertonic occurring within 6 months before the first dose of the study drug, or the glycosylated hemoglobin value ≥ 7.5% in the screening period.
• • 8. Severe or poorly controlled hypertension. 9. Bleeding symptoms with apparent clinical significance or obvious bleeding tendency within 1 months prior to the first dose of HS-20093 10. Serious arteriovenous thrombosis events occurred within 3 months before the first dose.
• • 11. Severe infections occurred within 4 weeks before the first dose. 12. Patients who have received continuous steroid treatment for more than 30 days within 30 days before the first dose, or need long-term (≥ 30 days) steroid treatment, or who have other acquired and congenital immunodeficiency diseases, or have a history of organ transplantation 13. The presence of active infectious diseases has been known before the first dose such as hepatitis B, hepatitis C, tuberculosis, syphilis, or human immunodeficiency virus HIV infection, etc.
• • 14. Hepatic encephalopathy, hepatorenal syndrome, or Child-Pugh Grade B or more severe cirrhosis.
• • 15. Other moderate or severe lung diseases that may interfere with the detection or treatment of drug-related pulmonary toxicity or may seriously affect respiratory function.
• • 16. Previous history of serious neurological or mental disorders, including epilepsy, dementia or severe depression and any other status that may interfere in assessment.
• • 17. Women who are breastfeeding or pregnant or planned to be pregnant during the study period.
• • 18. Vaccination or hypersensitivity of any level within 4 weeks prior to the first dose of HS-20093 19. History of severe hypersensitivity reaction, severe infusion reaction or allergy to recombinant human or mouse derived proteins.
• • 20. Hypersensitivity to any ingredient of HS-20093. 21. Unlikely to comply with study procedures, restrictions, and requirements in the opinion of the investigator 22. Any disease or condition that, in the opinion of the investigator, would compromise subject safety or interfere with study assessments