πŸ›οΈ Verified NIH Record β€’ Updated 2025-11-02

A Safety Study of 212Pb-VMT-alpha-NET in Patients With Neuroendocrine Tumors (NCT06148636)

A Phase 1, First-in-human Clinical Trial of [212Pb] VMT-alpha-NET Using a Forward Dosimetric Planning Technique to Treat Refractory or Relapsed Neuroendocrine Tumors

πŸ”΅ Active, Not Recruiting Early Phase1 πŸ’Š Investigational Drug / Biologic Sponsor: David Bushnell

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

This is a safety study to determine the recommended dose to test in clinical trials. The study involves two treatments with 212Pb (212-lead) VMT-Ξ±-NET. This is a safety study only; it will most likely not provide therapeutic benefit.

Who can join: Review the eligibility criteria below.

Location: Holden Comprehensive Cancer Center at the University of Iowa β€” Iowa City, Iowa

Age range: 18 Years to 80 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 (1 Sites)

  • Holden Comprehensive Cancer Center at the University of Iowa β€” Iowa City, Iowa

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. Review the official NIH record below to find the coordinating site.
  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†—