๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2025-08-13

Pan-tumor MRD Study (NCT06605404)

Molecular Residual Disease in Solid Tumors: A Prospective Study to Collect Clinical Data and Biospecimens to Support Discovery and Development of Cancer Biomarkers

๐ŸŸข Recruiting Interventional Protocol ๐Ÿ“Š Observational Clinical Research Sponsor: Paradigm Health

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

The purpose of this observational study is to collect clinical information, blood, and tumor tissue samples from participants diagnosed with stage I, stage II, or operable stage III cancer in select solid tumors. The information collected will be used to develop tests to better understand cancer, for example, to improve cancer detection and to assess the risk of cancer coming back. Participants will receive routine standard of care from their doctor and their involvement is expected to last for approximately five and a half (5.5) years.

Who can join: Review the eligibility criteria below.

Location: Medical Oncology Associates of San Diego โ€” San Diego, California

Age range: 18 Years

๐Ÿงช Interventions in This Study

  • blood and tissue samples (DIAGNOSTIC_TEST)
  • blood and tissue samples (OTHER)

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 (2 Sites)

  • Medical Oncology Associates of San Diego โ€” San Diego, California
  • Taylor Cancer Research Center โ€” Maumee, Ohio

๐Ÿ“ž Contact the Study Coordinator

Phone: (888) 662-6367

Email: anosheh.afghahi@flatiron.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†—