Back to Trials
NCT07524348PHASE1Recruiting

A Trial to Investigate the Safety of E303 in Participants With Advanced Refractory Solid Tumors

Samsung Bioepis Co., Ltd.

Start Date

3/23/2026

Completion Date

7/1/2030

Summary

This is a Phase I trial to evaluate the safety, tolerability and efficacy of nectin-4 targeting antibody-drug conjugate (SBE303) in participants with advanced solid tumors

Eligibility Criteria

Age Range: 18 years to No maximum

Inclusion Criteria: * Histologically-confirmed, locally advanced (unresectable) or metastatic solid tumors with recurrence or progression during or after standard therapy, intolerance to standard therapy, refused to receive standard therapy, or for whom no standard therapy is available. Exclusion Criteria: * Have spinal cord compression or clinically active central nervous system metastases * Have leptomeningeal disease * Have thromboembolic or clinically significant bleeding events * Have significant cardiovascular disease * Have an active autoimmune disease

Interventions

DRUG

E303

Interested in This Trial?

Contact the trial locations directly using the information below to learn more about enrollment.

Expressing interest lets you review the study and consent before we connect you with the research site.

Conditions

Advanced Solid Tumors

Locations

Research Site

Scottsdale, Arizona 85258

United States

Research Site

Fairfax, Virginia 22031

United States

Research Site

Adelaide,

Australia

Research Site

Melbourne,

Australia

Research Site

Barcelona,

Spain

Research Site

Madrid,

Spain