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
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