Tests BL-B01D1 with a PD-1 antibody in advanced lung, nose-throat and solid cancers

Who can take part

• Sign the informed consent form voluntarily and follow the protocol requirements
• Any gender
• Age: ≥18 years old
• Expected survival time for 3 months or more
• Patients with locally advanced or metastatic non-small cell lung cancer or nasopharyngeal carcinoma confirmed by histopathology and/or cytology
• Subjects were able to provide 6-10 slides of archived tumor tissue samples or fresh tissue samples of primary or metastatic lesions within 2 years
• At least one measurable lesion meeting the RECIST v1.1 definition was required
• ECOG 0 or 1
• The toxicity of previous antineoplastic therapy has returned to ≤ grade 1 as defined by NCI-CTCAE v5.0
• No serious cardiac dysfunction, left ventricular ejection fraction 50% or higher
• screening period not allowed within 14 days before a blood transfusion, are not allowed to use any cell growth factor, and/or liters of platelet medicine, organ function level must conform to the requirements
• Coagulation function: international normalized ratio (INR) ≤1.5, and activated partial thromboplastin time (APTT) ≤1.5ULN
• The urine protein + 2 or 1000 mg / 24 h or less or less
• For premenopausal women with childbearing potential, a pregnancy test must be performed within 7 days before starting treatment, serum or urine must be negative for pregnancy, and must be non-lactating; All enrolled patients (male or female) were advised to use adequate barrier contraception throughout the treatment cycle and for 6 months after the end of treatment

Who cannot take part

• Anti-tumor therapy such as chemotherapy or biological therapy has been used within 4 weeks or 5 half-lives before the first dose; Mitomycin and nitrosoureas were administered within 6 weeks before the first dose; Fluorouracil class oral drugs, etc
• Unstable thrombotic events requiring therapeutic intervention within 6 months before screening; Infusion-related thrombosis was excluded
• Before transplant or allogeneic hematopoietic stem cell transplantation (Allo - HSCT)
• Subjects with clinically significant bleeding or obvious bleeding tendency within 4 weeks before signing the informed consent
• Had participated in another clinical trial within 4 weeks before the first dose
• Serious heart disease
• Active autoimmune and inflammatory diseases
• Before the first delivery within 5 years diagnosed as other malignant tumor
• Two antihypertensive drugs poorly controlled hypertension
• With a history of ILD, current ILD or suspected suffering from such diseases during screening
• Complicated with pulmonary diseases leading to severe respiratory function impairment
• Human immunodeficiency virus antibody positive, active tuberculosis, active hepatitis B virus infection or active hepatitis C virus infection
• Active infection requiring systemic therapy
• Other conditions for trial participation were not considered appropriate by the investigator
• Stage 1 EGFR-sensitive mutant non-small cell lung cancer patients with systemic chemotherapy; Stage 2 patients who had received previous systemic therapy
• Long QT, complete left bundle branch block, III degree atrioventricular block; Serious arrhythmia
• For restructuring or human mouse chimeric antibody on study of humanized anti-platelet antibody has a history of allergies or allergic to BL - B01D1 any supplementary material composition of patients
• In the second stage queue one signed informed consent before gene sequencing report suggests patients such as mutation of ALK fusion
• Patients with poor glycemic control
• There is a lot of serous cavity effusion, or have a serous cavity effusion and has symptoms, or poorly controlled serous cavity effusion patients
• Imaging studies suggest tumor has violated or package around the chest, neck, pharyngeal large blood vessels
• Active central nervous system of patients