๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-07-30

Study of RAS(ON) Inhibitors in Combination With Ivonescimab in Patients With Solid Tumors (NCT07397338)

A Phase 1/2 Open-Label, Multicenter Study of RAS(ON) Inhibitors in Combination With Ivonescimab With or Without Other Anti-Cancer Agents in Patients With Solid Tumors

๐ŸŸข Recruiting Phase1 / Phase2 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Revolution Medicines, Inc.

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

The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (PK), and preliminary antitumor activity of RAS(ON) inhibitors in combination with ivonescimab in adults with advanced or metastatic solid tumors with a RAS mutation.

Who can join: Review the eligibility criteria below.

Location: USC Norris Comprehensive Cancer Center โ€” Los Angeles, California

Age range: 18 Years

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 (9 Sites)

  • USC Norris Comprehensive Cancer Center โ€” Los Angeles, California
  • Eastern Connecticut Hematology and Oncology Associates โ€” Norwich, Connecticut
  • Health Partners Cancer Center at Regions Hospital โ€” Saint Paul, Minnesota
  • Tennessee Oncology โ€” Nashville, Tennessee
  • MD Anderson Cancer Center โ€” Houston, Texas
  • MD Anderson Cancer Center โ€” Houston, Texas
  • NEXT Dallas โ€” Irving, Texas
  • NEXT Oncology โ€” San Antonio, Texas
  • NEXT Virginia โ€” Fairfax, Virginia

๐Ÿ“ž Contact the Study Coordinator

Phone: (323) 865-0967

Email: Lorraine.Martinez@med.usc.edu

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†—