A Phase I/II Clinical Study of WJ22096 Tablets in Patients With Advanced Tumors

Who cannot join

• General Conditions 1) Pregnant or lactating women; 2) Known allergy or contraindication to any components of the study drug; 3) History of drug abuse; 4) History of alcohol abuse (alcoholism); 5) Difficulty with intravenous blood collection (e.g., history of needle phobia, hemophobia).
• Prior or Concomitant Therapies 1) Prior or current treatment with a FAK inhibitor; 2) Received systemic anti-tumor drug therapy (e.g., chemotherapy, targeted therapy, endocrine therapy) within 3 weeks prior to the first dose (or, if prior anti-tumor drug therapy was received, a washout period of 5 half-lives, whichever is longer), or radiotherapy within 3 weeks, or immunotherapy within 4 weeks prior to the first dose; 3) Use of Chinese herbal medicine with anti-tumor effects within 2 weeks prior to the first dose; 4) Concomitant use of moderate or strong inhibitors or inducers of CYP3A, or other products (e.g., grapefruit juice), or inhibitors or inducers of P-gp; or discontinuation of such agents for less than 5 half-lives or 14 days (whichever is longer) prior to the first dose; 5) Known history of organ transplant or stem cell transplant; major surgery within 4 weeks prior to the first dose, or planned surgery during the study period; 6) Radiotherapy within 21 days prior to administration (Exception: Patients who received radiotherapy to ≤5% of their bone marrow volume are eligible regardless of when the radiotherapy was received).
• Medical History, Current Conditions, and Laboratory Abnormalities 1) Active gastrointestinal (GI) abnormalities including, but not limited to: inability to take oral medication, requirement for IV nutritional support, peptic ulcers, chronic diarrhea (e.g., Crohn's disease, irritable bowel syndrome), or vomiting, or other factors that, in the investigator's opinion, may significantly affect drug absorption, metabolism, or excretion (e.g., small bowel stom); 2) Clinically uncontrolled third-space fluid accumulation, such as pleural effusion, pericardial effusion, ascites, or pelvic effusion, deemed unsuitable for enrollment by the Investigator; 3) Patients with active brain metastases, including symptomatic brain metastases, meningeal metastases, or spinal cord compression. However, the following patients are allowed: a. Patients with treated brain metastases (e.g., surgery, radiotherapy) who are radiologically stable for at least 4 weeks prior to the first dose, and/or have no new or progressive neurological symptoms or signs, no evidence of new or enlarging brain metastases, and have discontinued systemic corticosteroid therapy (dose >10 mg/day prednisone or equivalent) for at least 4 weeks prior to the first dose; b. Subjects with untreated, asymptomatic brain metastases who do not require corticosteroids; 4) Poorly controlled hypertension: systolic blood pressure ≥160 mmHg and/or diastolic blood pressure ≥100 mmHg during the screening period; 5) Uncontrolled diabetes mellitus (baseline fasting blood glucose >8.9 mmol/L or Glycosylated Hemoglobin (HbA1c) >6.5%); 6) Clinically significant bleeding symptoms or obvious bleeding tendency within 4 weeks prior to the first dose (e.g., gastrointestinal bleeding, peptic ulcer bleeding); 7) Active HBV or HCV infection: If HBsAg is positive or/and anti-HBc is positive, HBV DNA must be tested to confirm it is above the limit of quantitation; If anti-HCV is positive, HCV RNA must be tested to confirm HCV viral load is above the limit of quantitation; 8) Human Immunodeficiency Virus (HIV) infection or a known history of positive HIV serology; 9) History of syphilis with positive results for both specific (treponemal) and non-specific (non-treponemal) syphilis antibodies; 10) Presence of concurrent malignancies within 5 years prior to enrollment (Exceptions: adequately treated cervical carcinoma in situ, non-melanoma skin cancer or lentigo maligna, localized cutaneous squamous cell carcinoma, basal cell carcinoma, prostate cancer not requiring anti-tumor treatment, thyroid cancer, ductal carcinoma in situ of the breast, and urothelial carcinoma ≤T1); 11) Occurrence within 6 months prior to the first dose of: acute coronary syndrome, congestive heart failure (New York Heart Association [NYHA] functional class ≥II), left ventricular ejection fraction (LVEF) <50%, cerebrovascular accident, transient ischemic attack, stroke, deep vein thrombosis, pulmonary embolism, aneurysm, arterial dissection, or other Grade 3 or higher cardiovascular or cerebrovascular events; 12) Arrhythmias (e.g., bradyarrhythmias) or conduction abnormalities considered clinically significant by the Investigator, congenital long QT syndrome, or unmeasurable or Fridericia's-corrected QTc >450 ms for males or >470 ms for females; 13) Presence of persistent or severe active infectious diseases (including bacterial, fungal, viral, etc.) requiring intravenous anti-infective therapy; 14) Known or suspected refractory urinary tract infection (UTI) or a history of recurrent UTIs (≥3 episodes in the past 12 months); 15) Any other condition that, in the opinion of the investigator, may affect study results or interfere with full participation in the study.