๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-08-10

SMP-3124LP in Adults With Advanced Solid Tumors (NCT06526819)

An Open-label, Phase 1 Dose Escalation and Phase 2 Dose Expansion Study to Assess Safety, Tolerability, Pharmacokinetics, and Preliminary Antitumor Activity of SMP-3124LP in Adults With Advanced Solid Tumors

๐ŸŸข Recruiting Phase1 / Phase2 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Sumitomo Pharma America, Inc.

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

An Open-label, Phase I Dose Escalation and Phase 2 Dose Expansion Study to Assess Safety, Tolerability, Preliminary Antitumor Activity of SMP 3124LP in Adults with Advanced Solid Tumors

Who can join: Review the eligibility criteria below.

Location: Cedars Sinai Medical Center โ€” Los Angeles, 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 (12 Sites)

  • Cedars Sinai Medical Center โ€” Los Angeles, California
  • Sarah Cannon Research Institute at HealthOne โ€” Denver, Colorado
  • Advent Health โ€” Celebration, Florida
  • Northwestern Medicine Cancer Center โ€” Chicago, Illinois
  • The University of Chicago โ€” Chicago, Illinois
  • Ohio State University โ€” Columbus, Ohio
  • SCRI Oncology Partners โ€” Nashville, Tennessee
  • Vanderbilt-Ingram Cancer Center โ€” Nashville, Tennessee
  • MD Anderson Cancer Center โ€” Houston, Texas
  • University of Washington โ€” Seattle, Washington
  • National Cancer Center Hospital East โ€” Kashiwa-shi,
  • Kyoto University Hospital โ€” Kyoto,

๐Ÿ“ž Contact the Study Coordinator

Phone: (774) 405-5069

Email: eileen.maunsell@us.sumitomo-pharma.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.

Explore by condition: All Solid Tumor clinical trials

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†—