A Clinical Study of [177Lu]Lu-XT117 Injection in Patients With Advanced Solid Tumors

Key Inclusion Criteria: * ≥18 years old * Eastern Cooperative Oncology Group (ECOG) Performance status 0 to 1 * Confirmed as malignant solid tumor by histopathology * Have measurable lesions based on RECIST 1.1 * Have failed standard treatment (disease progression or intolerance) or lack standard treatment * Positive FAP expression confirmed by FAP PET/CT * Sufficient bone marrow capacity and organ function Key Exclusion Criteria: * High intensity and large amounts of off-target uptake by FAP molecular imaging, and were assessed as inappropriate for \[177Lu\]Lu-XT117 therapy by the investigators * Previous systemic antitumor therapy (including prior chemotherapy, radiotherapy, immunotherapy, and other investigational drugs) ≤28 days before receiving study therapy; previous treatment with Chinese medicine with anti-tumor indications within 2 weeks before receiving study therapy * Uncontrolled diabetes, with baseline fasting blood glucose \> 2×ULN * Clinically significant serious cardiovascular disease, including but not limited to: a. \>Grade II congestive heart failure as per New York Heart Association (NYHA) ; b. Unstable angina pectoris or myocardial infarction within 6 months before the first administration of the study drug; c. Severe arrhythmia within 6 months prior to the first administration; d. Poorly controlled hypertension (patients who keep the blood pressure to ≤ Grade 2 hypertension \[CTCAE5.0\] with hypotensor are allowed for enrollment); e. QTc\>450 ms (male) or 470 ms (female), congenital prolonged QT syndrome, and use of medications that prolong QT * Clinically serious thromboembolic disease within 6 months prior to the first administration of the study drug * Major surgery within 4 weeks prior to the initial administration of the study drug * History of severe gastrointestinal ulcers or perforations or history of intestinal obstruction within 6 months prior to the first administration * Active infection requiring systemic treatment (oral or intravenous administration) within 2 weeks prior to the first administration, except for topical treatment * History of non-infectious interstitial lung disease (ILD), such as idiopathic pulmonary fibrosis, idiopathic interstitial pneumonia, pneumoconiosis, and drug-related interstitial pneumonia, or severe impairment of lung function * Had other malignancies within 5 years prior to screening (except clinically cured early stage malignancies) * Primary central nervous system (CNS) tumor or symptomatic CNS metastasis, expect: * Subjects with asymptomatic brain metastases; * Subjects whose CNS lesions were stable for ≥4 weeks after local treatment and who stopped glucocorticoid or anticonvulsant therapy at least 2 weeks prior to study drug administration could be enrolled; * Uncontrolled pleural effusion, pericardial effusion, or ascites requiring repeated drainage