A Study of BL-B01D1 Combined With Lenvatinib in Patients With Advanced Hepatocellular Carcinoma

Launched by SICHUAN BAILI PHARMACEUTICAL CO., LTD. · May 21, 2025

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ClinConnect Summary

This clinical trial is studying a new treatment approach for patients with advanced liver cancer, specifically hepatocellular carcinoma (HCC). Researchers want to find out if combining two medications, BL-B01D1 and lenvatinib, is effective and safe for patients. The trial is not yet open for enrollment, but it aims to include adults aged 18 to 75 who have been diagnosed with advanced HCC and have measurable tumors. Participants will need to provide consent and may have to provide tissue samples from their tumors. It's important that potential participants do not have severe heart issues or other serious health conditions that could complicate treatment.

If you or a loved one qualify for this trial, you can expect to receive careful monitoring throughout the study. The goal is to see how well the combination of these two drugs works and to understand the side effects. Participants will also be required to use effective birth control if they are of childbearing age. This trial provides an opportunity to access new treatments that may help manage this challenging condition, but it’s essential to discuss any questions or concerns with a healthcare provider before deciding to participate.

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Eligibility criteria

• Inclusion Criteria:
• • 1. Sign the informed consent form voluntarily and follow the protocol requirements;
• • 2. Gender is not limited;
• • 3. Age ≥18 years old and ≤75 years old;
• • 4. Expected survival time ≥3 months;
• • 5. Patients with advanced HCC confirmed by histology or cytology;
• • 6. Consent to provide archived tumor tissue samples or fresh tissue samples from the primary or metastatic lesions;
• • 7. At least one measurable lesion meeting the RECIST v1.1 definition was required;
• • 8. ECOG score was 0-1;
• • 9. The toxicity of previous antineoplastic therapy has returned to ≤ grade 1 as defined by NCI-CTCAE v5.0;
• • 10. No severe cardiac dysfunction, left ventricular ejection fraction ≥50%;
• • 11. Organ function level must meet the requirements;
• • 12. Coagulation function: international normalized ratio (INR) ≤1.5×ULN, and activated partial thromboplastin time (APTT) ≤1.5×ULN;
• • 13. Urinary protein ≤2+ or ≤1000mg/24h;
• • 14. No cirrhosis or only Child-Pugh A cirrhosis;
• • 15. If hepatitis B virus infection is negative or positive, the status of HBV surface antigen (HBsAg) should be confirmed by HBV serological test;
• • 16. For premenopausal women of childbearing potential, a pregnancy test must be performed within 7 days before the start of treatment, a serum or urine pregnancy test must be negative, and the patient must not be lactating; All enrolled patients should take adequate barrier contraception during the entire treatment cycle and for 6 months after the end of treatment.
• Exclusion Criteria:
• • 1. Patients with active central nervous system metastases;
• • 2. Who had participated in any other clinical trial within 4 weeks before the trial dose;
• • 3. Received anti-tumor therapy such as chemotherapy, radiotherapy and biological therapy within 4 weeks before the first use of study drug;
• • 4. Had undergone major surgery (investigator-defined) within 4 weeks before the first dose;
• • 5. Systemic corticosteroids or immunosuppressive therapy is required within 2 weeks before study dosing;
• • 6. Pulmonary disease defined as ≥ grade 3 according to NCI-CTCAE v5.0; A history of ILD/pulmonary inflammation requiring steroid treatment;
• • 7. Serious systemic infection within 4 weeks before screening;
• • 8. Patients at risk for active autoimmune disease or with a history of autoimmune disease;
• • 9. Other malignant tumors within 5 years before the first treatment;
• • 10. Human immunodeficiency virus antibody positive, active tuberculosis or hepatitis C virus infection;
• • 11. Poorly controlled hypertension by two antihypertensive drugs with different mechanisms;
• • 12. Diabetic patients with poor glycemic control;
• • 13. Had a history of severe cardiovascular and cerebrovascular diseases;
• • 14. Previous history of autologous or allogeneic stem cell, bone marrow or organ transplantation;
• • 15. Subjects with clinically significant bleeding or significant bleeding tendency within the previous 4 weeks were screened;
• • 16. Patients with massive or symptomatic effusions or poorly controlled effusions;
• • 17. Imaging examination showed that the tumor had invaded or wrapped around the chest, neck, pharynx and other large arteries or invaded the pericardium and heart;
• • 18. Unstable thrombotic events requiring therapeutic intervention within 6 months before screening;
• • 19. Prior treatment with an ADC drug with a topoisomerase I inhibitor as a toxin;
• • 20. Patients with a history of allergy to recombinant humanized antibodies or to any excipients of the trial drug;
• • 21. The cumulative dose of anthracyclines \> 360 mg/m2 in previous (new) adjuvant therapy;
• • 22. Pregnant or lactating women;
• • 23. Who have a history of psychotropic drug abuse and cannot quit or have mental disorders;
• • 24. Other conditions for trial participation were not considered appropriate by the investigator.