RecruitingPhase 1Phase 2NCT06639347

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

An Open Label, Multicenter, Phase Ib/Il Study to Evaluate the Safety, Tolerability, and Efficacy of SHR A2102 in Combination With Other Anti-cancer Agents in Patients With Advanced Urothelial Carcinoma

Sponsor

Shanghai Hengrui Pharmaceutical Co., Ltd.

Enrollment

90 participants

Start Date

Nov 4, 2024

Study Type

INTERVENTIONAL

Conditions

Advanced Urothelial Carcinoma

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

Min Age: 18 Years

Inclusion Criteria7

Competent to comprehend, sign, and date an informed consent form.
Male or female subjects must be age 18 or older.
Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
Subjects must have histologically documented, unresectable locally advanced or
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.
An archival tumor tissue sample or a fresh tissue sample should be provided.
Subjects must have measurable disease according to RECIST (version 1.1).

Exclusion Criteria11

Subjects with not adequately treated, or uncontrollable , or active CNS metastases.
Subjects who have previously received TOPO1-based ADCs.
Subjects who have received anti-cancer treatment within 4 weeks prior the first dose of study treatment.
Subjects who have received radiotherapy within 14 days , or chest radiotherapy > 30Gy within 6 months prior to the first dose of study drug.
Subjects with ongoing clinically significant toxicity associated with prior treatment that has not resolved to ≤ Grade 1.
Subjects who have received systemic immunosuppressant treatment within 14 days prior the first dose of study treatment.
Subjects who have known or suspected interstitial pneumonitis.
Phase Ib: Subjects who have had≥ Grade 3 irAEs during the previous treatment with ICIs.
Subjects who have any active, known or suspected autoimmune diseases.
Subjects who have moderate or severe ascites with clinical symptoms, or uncontrolled or moderate or above pleural effusion, or pericardial effusion.
Subjects who have uncontrolled cardiac diseases or cardiac clinical symptoms.