NCT06639347 A Trial of SHR-A2102 With Antitumor Therapy in Advanced Urothelial Carcinoma

Eligibility & Interventions

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

Phase 1 is the earliest stage of human testing — safety and dosage are the primary focus. Visits are frequent and medical supervision is intensive. You will be among the first people to receive this treatment.

This trial targets 90 participants in total. It began in 2024-11-04 with a primary completion date of 2027-05-31.

Brief Summary

The study is being conducted to evaluate the safety, tolerability and efficacy of SHR-A2102 for injection with Antitumor Therapy in Advanced Urothelial Carcinoma. To explore the reasonable dosage of SHR-A2102 for Advanced Urothelial Carcinoma.

Eligibility Criteria

Inclusion Criteria: 1. Competent to comprehend, sign, and date an informed consent form. 2. Male or female subjects must be age 18 or older. 3. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1. 4. Subjects must have histologically documented, unresectable locally advanced or 5. Histologically confirmed locally advanced or metastatic urothelial cancer.Phase Ib, subjects must have failed, be intolerant or refused the standard treatment; Phase II, subjects must not have received systemic antitumor therapy for locally advanced unresectable or metastatic urothelial carcinoma. 6. An archival tumor tissue sample or a fresh tissue sample should be provided. 7. Subjects must have measurable disease according to RECIST (version 1.1). Exclusion Criteria: 1. Subjects with not adequately treated, or uncontrollable , or active CNS metastases. 2. Subjects who have previously received TOPO1-based ADCs. 3. Subjects who have received anti-cancer treatment within 4 weeks prior the first dose of study treatment. 4. Subjects who have received radiotherapy within 14 days , or chest radiotherapy \> 30Gy within 6 months prior to the first dose of study drug. 5. Subjects with ongoing clinically significant toxicity associated with prior treatment that has not resolved to ≤ Grade 1. 6. Subjects who have received systemic immunosuppressant treatment within 14 days prior the first dose of study treatment. 7. Subjects who have known or suspected interstitial pneumonitis. 8. Phase Ib: Subjects who have had≥ Grade 3 irAEs during the previous treatment with ICIs. 9. Subjects who have any active, known or suspected autoimmune diseases. 10. Subjects who have moderate or severe ascites with clinical symptoms, or uncontrolled or moderate or above pleural effusion, or pericardial effusion. 11. Subjects who have uncontrolled cardiac diseases or cardiac clinical symptoms.

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