πŸ›οΈ Verified NIH Record β€’ Updated 2026-07-27

Phase I Study of [225Ac]Ac-ETN029 in Patients With Advanced DLL3-expressing Solid Tumors (NCT07006727)

A Phase I, Open-label, Multi-center Study to Evaluate the Safety, Tolerability, Dosimetry, and Preliminary Activity of [225Ac]Ac-ETN029 in Patients With Advanced DLL3-expressing Solid Tumors

🟒 Recruiting Phase1 πŸ’Š Investigational Drug / Biologic Sponsor: Novartis Pharmaceuticals

🩺 Plain-English Summary (8th-Grade Level)

The purpose of this study is to evaluate the safety, tolerability, dosimetry and preliminary efficacy of \[225Ac\]Ac-ETN029 and the safety and imaging properties of \[111In\]In-ETN029 in patients aged β‰₯ 18 years with locally advanced or metastatic DLL3 positive cancers.

Who can join: Review the eligibility criteria below.

Location: University Of Iowa β€” Iowa City, Iowa

Age range: 18 Years to 100 Years

πŸ§ͺ Interventions in This Study

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

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

πŸ“ All Participating Trial Locations (7 Sites)

  • University Of Iowa β€” Iowa City, Iowa
  • Massachusetts General Hospital β€” Boston, Massachusetts
  • Corewell Health William Beaum Hosp β€” Royal Oak, Michigan
  • Fred Hutchinson Cancer Research Center β€” Seattle, Washington
  • Novartis Investigative Site β€” Montreal, Quebec
  • Novartis Investigative Site β€” Seoul, Seoul
  • Novartis Investigative Site β€” Seoul,

πŸ“ž Contact the Study Coordinator

Phone: (888) 669-6682

Email: novartis.email@novartis.com

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

πŸ’° 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 Β§ 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.

πŸ’‘ 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.
πŸ›οΈ View Official NIH Record β†—