ADCE-T02, a Tissue Factor Targeted Antibody-Drug Conjugate, in Patients With Selected Advanced Solid Tumours

Eligibility Criteria

• 1. Patients must have pathologically confirmed unresectable advanced solid tumor.
• 2. Patients who have undergone at least one systemic therapy and have progressive disease
• 3. Patients must have at least one measurable lesion as per RECIST version 1.1.
• 4. Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.
• 5. Life expectancy ≥ 3 months.
• 6. Patients must have adequate organ function as indicated by laboratory values
• 7. Women of childbearing potential (WCBP), defined as sexually mature women who have not undergone surgical sterilization or who have not been naturally postmenopausal for at least 12 consecutive months must agree to use two effective contraceptive methods while on study treatment and for at least 7 months after the last dose of ADCE T02.
• 8. Male patients must agree to use condoms, even if they have had a successful vasectomy, while on study treatment and for at least 4 months after the last dose of ADCE T02.
• 1. Prior treatment with any agent targeting Tissue Factor
• 2. Central nervous system (CNS) metastasis.
• 3. Active ocular surface disease or a history of cicatricial conjunctivitis or inflammatory conditions that predispose to cicatrizing conjunctivitis, mucus pemphigoid or penetrating ocular transplants.
• 4. Persistent toxicities from previous systemic anti-neoplastic treatments
• 5. Known past or current coagulation defects leading to an increased risk of bleeding
• 6. Significant cardiac disease; recent myocardial infarction, acute coronary syndromes, congestive heart failure , uncontrolled hypertension, uncontrolled cardiac arrhythmias
• 7. History of (non-infectious) interstitial lung disease (ILD)/pneumonitis that required steroids, or current ILD/pneumonitis, or suspected ILD/pneumonitis
• 8. Prior history of malignancy other than inclusion diagnosis within five years prior to first dose of ADCE T02.