Study of HS-20093 Versus Gemcitabine in Combination With Docetaxel in Treatment of Osteosarcoma After Previous Second-line Treatment Failure

Launched by HANSOH BIOMEDICAL R&D COMPANY · Apr 17, 2025

Keywords

ClinConnect Summary

This clinical trial is studying a new treatment called HS-20093 to see how well it works compared to a combination of two existing medications, gemcitabine and docetaxel, in treating osteosarcoma. Osteosarcoma is a type of bone cancer that can be challenging to treat, especially after previous treatments have failed. The trial is designed for patients aged 12 and older who have been diagnosed with osteosarcoma and have at least one tumor that can be measured. Participants must also be in relatively good health to join the study.

If you or someone you know is considering joining this trial, it’s important to note that there are specific eligibility criteria. For example, participants should not have had certain previous cancer treatments or serious health issues that could complicate their participation. The trial is not yet recruiting, so there’s still time to learn more before getting involved. Throughout the study, participants will receive either HS-20093 or the combination treatment and will be monitored closely for safety and effectiveness. This research aims to find better options for patients who have limited choices due to treatment failures.

Gender

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Eligibility criteria

• Inclusion Criteria:
• • Males or females over 12 years old (≥ 12 years).
• • Pathologically confirmed osteosarcoma (key IHC/tumor cell phenotyping results required for a definitive diagnosis must be provided).
• • The study participants should have at least 1 target lesion based on RECIST 1.1.
• • An ECOG PS of 0 to 1, with no exacerbation within two weeks prior to first dosing.
• • A minimum expected survival of greater than 12 weeks.
• • Female study participants of childbearing potential must be willing to use appropriate contraceptive measures and refrain from breastfeeding from the signing of informed consent to six months after the last dosing or the end of treatment (whichever occurs later); male study participants must be willing to use barrier contraceptive measures (i.e., condoms) from the signing of informed consent to six months after the last dosing or the end of treatment (whichever occurs later).
• * Female study participants must provide negative blood or urine pregnancy test results within seven days before the first dosing, or meet one of the following criteria to prove there is no risk of pregnancy:
• • Voluntary participation in this clinical trial, and signing and dating of the written ICF approved by the IRB/IEC in accordance with regulatory, local, and institutional guidelines.
• Exclusion Criteria:
• * Prior or ongoing therapies as follows:
• • 1. Prior or current use of treatments targeting B7-H3
• • 2. Prior or current use of treatments with topoisomerase I inhibitors, including antibody-drug conjugates that are effectively loaded with topoisomerase I inhibitors
• • 3. Prior or current use of systemic anti-tumor therapy with gemcitabine in combination with docetaxel;
• • 4. Use of cytotoxic chemotherapy drugs, experimental drugs, traditional Chinese medicines for anti-tumor indicationsor other anti-tumor drugs within 14 days prior to randomization; or requiring continued use of such drug therapies during the study;
• • 5. Use of macromolecular anti-tumor drug therapy within 28 days prior to randomization;
• • Presence of residual grade ≥ 2 toxicities by Common Terminology Criteria for Adverse Events (CTCAE version 5.0) from previous treatments.
• • History of other primary solid tumors.
• * Inadequate bone marrow reserve or liver and kidney organ function, which meets any of the following laboratory limits:
• • Serious, uncontrolled or active cardiovascular diseases.
• • Severe or poorly controlled diabetes, including: ① Diabetic ketoacidosis or hyperglycemia and hyperosmolarity within 6 months prior to randomization; or ② other severe or poorly controlled diabetes conditions as determined by the investigator.
• • Severe or poorly controlled hypertension, including: history of prior hypertensive crisis or hypertensive encephalopathy; adjustment of antihypertensive drug therapy within two weeks prior to randomization due to poor blood pressure control; systolic blood pressure ≥ 180 mmHg or diastolic blood pressure ≥ 110 mmHg during the screening period.
• • Have clinically significant hemorrhage symptoms or significant hemorrhagic diathesis within 1 month before randomization.
• • Serious arteriovenous thrombotic events within 3 months before randomization, such as deep vein thrombosis, pulmonary embolism, etc. .
• • Severe infection within four weeks prior to randomization, including but not limited to complications of infection, bacteremia, or severe pneumonia requiring intravenous antibiotic therapy for ≥ 2 weeks; or uncontrollable active infection during the screening period. Study participants who are receiving or have received prophylactic antibiotics may be enrolled.
• • Patients who have received continuous glucocorticoid therapy for more than 30 days within 30 days before randomization, or who require long-term (≥ 30 days) use of glucocorticoids, or patients with other acquired/congenital immunodeficiency diseases or with a history of transplantation (except for corneal transplantation). Systemic corticosteroids (≤ 10 mg/d prednisone or equivalent) at a physiological replacement dose are permitted.
• • Known presence of infectious diseases, such as hepatitis B , hepatitis C, tuberculosis , syphilis, or HIV infection , etc. Active infectious diseases will not be screened for proactively.
• • Existing hepatic encephalopathy, hepatorenal syndrome, or ≥ Child-Pugh class B cirrhosis.
• • Known interstitial pneumonia or immune pneumonitis, other moderate-to-severe lung diseases that may interfere with the detection or treatment of drug-related pulmonary toxicity and severely affect respiratory function.
• • A history of prior serious neurological or psychiatric disorders, including epilepsy, dementia, severe depression, or other conditions that can interfere with the assessment.
• • Female patients who are pregnant, breastfeeding, or planning to become pregnant during the study.
• • Vaccination or occurrence of any degree of allergic or hypersensitivity reaction within four weeks prior to the first dosing.
• • Subjects who have previously experienced severe allergies or serious infusion reactions, or who are allergic to recombinant humanized or murine protein substances.
• • ‬Allergies to any component of the study drug HS-20093 , gemcitabine and its excipients, and docetaxel and its excipients.
• • Patients who may have poor compliance with the study procedures and requirements as judged by the investigator.
• • Patients with any condition that, in the Investigator's judgment, jeopardizes their safety or interferes with study assessments.