A Dose Escalation and Expansion Study of XB371 Administered in Participants With Locally Advanced or Metastatic Solid Tumors
Exelixis
Summary
The primary purpose of the study is to characterize the safety and tolerability of XB371. The dose-escalation cohorts and Part B of the expansion cohorts are non-randomized. Part A of the expansion cohorts is randomized.
Eligibility
- Age range
- 18+ years
- Sex
- All
- Healthy volunteers
- No
Key Inclusion Criteria: * Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1. * Minimum life expectancy of ≥ 12 weeks. * Recurrent locally advanced or metastatic solid tumors. * Adequate end organ and bone marrow function. Key Exclusion Criteria: * Primary brain tumors or known active brain metastases, leptomeningeal, or cranial epidural disease. * History of interstitial lung disease (ILD) of any grade or history of organizing pneumonia. * Has acute ocular infection, acute or chronic ulcerative/cicatricial condition of conjunctiva or cornea. * Known history of immunodef…
Interventions
- DrugXB371
Intravenous (IV) infusion.
Locations (9)
- Exelixis Clinical Site #5Rogers, Arkansas
- Exelixis Clinical Site #9Los Angeles, California
- Exelixis Clinical Site #6Washington D.C., District of Columbia
- Exelixis Clinical Site #4Orlando, Florida
- Exelixis Clinical Site #3Grand Rapids, Michigan
- Exelixis Clinical Site #7New Brunswick, New Jersey