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NOT YET RECRUITING
NCT07907861
PHASE2

Sacituzumab Tirumotecan Plus Toripalimab for Advanced Penile Cancer After Platinum Chemotherapy

Sponsor: Anhui Provincial Hospital

View on ClinicalTrials.gov

Summary

This is a single-center, single-arm, open-label, Phase 2 clinical trial (the SCOPE study) evaluating the efficacy, safety, and tolerability of sacituzumab tirumotecan (SKB264) combined with toripalimab as a second-line, chemo-free treatment for patients with unresectable locally advanced or metastatic penile squamous cell carcinoma whose disease progressed on or who are intolerant to platinum-based chemotherapy. Penile squamous cell carcinoma (PSCC) is a rare and aggressive cancer with limited treatment options once disease progression occurs after initial platinum-based chemotherapy, and standard second-line approaches leave tumors shrinking or disappearing in only 10-15% of cases. Sacituzumab tirumotecan is an antibody-drug conjugate (ADC) designed to target TROP-2, a protein expressed on the surface of nearly all penile cancer cells. By binding to TROP-2, sacituzumab tirumotecan delivers a chemotherapy payload directly to the tumor cells. Toripalimab is an immunotherapy drug (a PD-1 inhibitor) that helps the body's immune system find and attack cancer cells, and combining an ADC with a PD-1 inhibitor may work better than either drug alone. All participants in this trial will receive both study drugs via intravenous (IV) infusion on Day 1 of each 2-week cycle, toripalimab first, followed by sacituzumab tirumotecan about 30 minutes later, for as long as the treatment is helping them and the side effects are tolerable. The main goal of this study is to determine the percentage of participants whose tumors shrink or disappear after receiving the combination (Objective Response Rate). The study will also measure how long the responses last (Duration of Response), how long participants live without their cancer getting worse (Progression-Free Survival), how long participants live overall (Overall Survival), the percentage of participants whose disease is controlled (Disease Control Rate), and the side effects of the combination.

Official title: A Phase II, Single-center, Open-label Study of Sacituzumab Tirumotecan Combined With Toripalimab in Patients With Advanced Penile Squamous Cell Carcinoma Who Progressed On or Are Intolerant to Platinum-based Chemotherapy

Key Details

Gender

MALE

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

31

Start Date

2027-01-01

Completion Date

2030-01-01

Last Updated

2026-10-30

Healthy Volunteers

No

Interventions

DRUG

Sacituzumab Tirumotecan (SKB264)

Sacituzumab tirumotecan (SKB264) is a TROP2-targeted antibody-drug conjugate, administered intravenously at 4 mg/kg on Day 1 of each 2-week cycle.

DRUG

Toripalimab

Toripalimab is a PD-1 inhibitor, administered intravenously at 3 mg/kg on Day 1 of each 2-week cycle. No dose reduction is performed; immune-related adverse events are managed by continuing treatment, holding, or permanently discontinuing the drug according to severity.

Locations (1)

The First Affiliated Hospital of University of Science and Technology of China (West Campus) (Anhui Provincial Cancer Hospital)

Hefei, Anhui, China