๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-06-17

Study of XB010 in Subjects With Solid Tumors (NCT06545331)

A Dose-Escalation and Expansion Study of XB010 as a Single Agent and Combination Therapy in Subjects With Locally Advanced or Metastatic Solid Tumors

๐ŸŸข Recruiting Phase1 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Exelixis

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

This is a FIH study is to evaluate the safety, tolerability, PK, immunogenicity, and preliminary antitumor activity of XB010 as a single agent and in combination with pembrolizumab in subjects with locally advanced or metastatic solid tumors for whom alternative therapies do not exist or available therapies are intolerable or no longer effective.

Who can join: Review the eligibility criteria below.

Location: City of Hope Orange County Lennar Foundation Cancer Center โ€” Irvine, California

Age range: 18 Years

๐Ÿงช Interventions in This Study

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (20 Sites)

  • City of Hope Orange County Lennar Foundation Cancer Center โ€” Irvine, California
  • UCLA Department of Medicine - Hematology/Oncology โ€” Los Angeles, California
  • Georgetown University Medical Center โ€” Washington D.C., District of Columbia
  • Sarah Cannon Research Institute at Florida Cancer Specialists โ€” Orlando, Florida
  • Winship Cancer Institute โ€” Atlanta, Georgia
  • University of Chicago Medical Center โ€” Chicago, Illinois
  • Siteman Cancer Center โ€” St Louis, Missouri
  • Montefiore Medical Center - Montefiore Medical Park โ€” The Bronx, New York
  • Carolina BioOncology Institute โ€” Huntersville, North Carolina
  • Stephenson Cancer Center โ€” Oklahoma City, Oklahoma
  • SCRI Oncology Partners โ€” Nashville, Tennessee
  • NEXT Austin โ€” Austin, Texas
  • Baylor University Medical Center โ€” Dallas, Texas
  • University of Texas MD Anderson Cancer Center โ€” Houston, Texas
  • Inova Schar Cancer โ€” Fairfax, Virginia
  • NEXT Virginia โ€” Fairfax, Virginia
  • University Hospitals of Leicester NHS Trust โ€” Leicester,
  • Sarah Cannon Research Institute London โ€” London,
  • University College London Hospitals NHS Foundation Trust โ€” London,
  • The Christie NHS Foundation Trust โ€” Manchester,

๐Ÿ“ž Contact the Study Coordinator

Phone: 1-888-EXELIXIS (888-393-5494)

Email: druginfo@exelixis.com

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—