๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2025-12-02

A Study of ERAS-4001 in Patients With Advanced or Metastatic Solid Tumors. (NCT07021898)

A Phase 1 First-in-Human Open-label Study Evaluating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Preliminary Efficacy of ERAS-4001 Monotherapy and in Combination in Patients With Advanced Solid Tumors

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

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

The main purpose of the study is to assess whether the study drug, ERAS-4001, is safe and tolerable when administered to patients with advanced or metastatic solid tumors with certain KRAS mutations. ERAS-4001 will be given alone or in combination with other treatments.

Who can join: Review the eligibility criteria below.

Location: Sarah Cannon Research Institute (SCRI) Oncology Partners โ€” Nashville, Tennessee

Age range: 18 Years to 99 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 (5 Sites)

  • Sarah Cannon Research Institute (SCRI) Oncology Partners โ€” Nashville, Tennessee
  • The University of Texas MD Anderson Cancer Center โ€” Houston, Texas
  • NEXT Oncology โ€” Irving, Texas
  • NEXT Oncology โ€” San Antonio, Texas
  • Fred Hutchinson Cancer Center โ€” Seattle, Washington

๐Ÿ“ž Contact the Study Coordinator

Phone: (858) 465-6511

Email: clinicaltrials@erasca.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†—