๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-07-09

A Study of ELI-002 7P in Subjects With KRAS/NRAS Mutated Solid Tumors (NCT05726864)

First in Human Phase 1/2 Trial of ELI-002 7P Immunotherapy as Treatment for Subjects With Kirsten Rat Sarcoma (KRAS)/Neuroblastoma RAS Viral Oncogene Homolog (NRAS) Mutated Pancreatic Ductal Adenocarcinoma (PDAC) and Other Solid Tumors

๐Ÿ”ต Active, Not Recruiting Phase1 / Phase2 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Elicio Therapeutics

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

This is a Phase 1/2 study to assess the safety and efficacy of ELI-002 7P immunotherapy (a lipid-conjugated immune-stimulatory oligonucleotide \[Amph-CpG-7909\] plus a mixture of lipid-conjugated peptide-based antigens \[Amph-Peptides 7P\]) as adjuvant treatment in subjects with solid tumors with mutated KRAS/NRAS. This study builds on the experience obtained with related product ELI-002 2P, which was studied in protocol ELI-002-001 under IND 26909.

Who can join: Review the eligibility criteria below.

Location: Banner MD Anderson Cancer Center โ€” Gilbert, Arizona

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 (28 Sites)

Showing the first 25 of 28 sites.

  • Banner MD Anderson Cancer Center โ€” Gilbert, Arizona
  • Mayo Clinic Comprehensive Cancer Center โ€” Phoenix, Arizona
  • City of Hope โ€” Duarte, California
  • Cedars-Sinai Medical Center โ€” Los Angeles, California
  • University of California Los Angeles โ€” Los Angeles, California
  • University of California, Irvine โ€” Orange, California
  • University of Colorado Hospital-Anschutz Cancer Pavillion โ€” Aurora, Colorado
  • University of Miami โ€” Coral Gables, Florida
  • University of Florida Health Cancer Center โ€” Gainesville, Florida
  • Mayo Clinic Comprehensive Cancer Center โ€” Jacksonville, Florida
  • Moffitt Cancer Center โ€” Tampa, Florida
  • Emory Winship Cancer Institute โ€” Atlanta, Georgia
  • University of Iowa โ€” Iowa City, Iowa
  • Ochsner Health โ€” New Orleans, Louisiana
  • Massachusetts General Hospital โ€” Boston, Massachusetts
  • Dana Farber Cancer Institute โ€” Boston, Massachusetts
  • University of Michigan โ€” Ann Arbor, Michigan
  • Mayo Clinic Comprehensive Cancer Center โ€” Rochester, Minnesota
  • Northwell Health โ€” Lake Success, New York
  • Memorial Sloan Kettering Cancer Center โ€” New York, New York
  • New York Presbyterian Weill Cornell Medical Center โ€” New York, New York
  • Lehigh Valley Health Network โ€” Allentown, Pennsylvania
  • University of Pennsylvania โ€” Philadelphia, Pennsylvania
  • Sarah Cannon Research Institute โ€” Nashville, Tennessee
  • Vanderbilt University Medical Center โ€” Nashville, Tennessee

๐Ÿ“ž Contact the Study Coordinator

Phone: (877) 632-6789

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†—