๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-04-14

ARTIDIS Nanomechanical Generated Measurements for Early Breast Lesions (NCT06085833)

ARTIDIS Nanomechanical Generated Measurements for Early Breast Lesions (ANGEL)

๐ŸŸข Recruiting Observational / Diagnostic ๐Ÿ“‹ Clinical Research Protocol Sponsor: ARTIDIS AG

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

This prospective, blinded, single-arm study aims to test the performance of nanomechanical phenotype in predicting tumor type, tumor aggressiveness, and neoadjuvant treatment response compared to the gold standard of histopathological assessment. The study involves patients with suspicious breast lesions who will undergo a breast biopsy procedure indicated by standard of care. The nanomechanical phenotype will be measured on the freshly obtained breast biopsies or tissue from breast surgeries.

Who can join: Review the eligibility criteria below.

Location: University of Texas Southwestern Medical Center โ€” Dallas, Texas

Age range: 18 Years

๐Ÿงช Interventions in This Study

  • Nanomechanical Phenotype Test (DIAGNOSTIC_TEST)

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 (5 Sites)

  • University of Texas Southwestern Medical Center โ€” Dallas, Texas
  • Baylor College of Medicine โ€” Houston, Texas
  • MD Anderson Cancer Clinic - Mays Clinic โ€” Houston, Texas
  • Hospital Universitario Vall d'Hebron โ€” Barcelona, Barcelona
  • Claraspital โ€” Basel, Basel

๐Ÿ“ž Contact the Study Coordinator

Phone: (240) 498-0176

Email: julia.ortega@artidis.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 Breast Cancer 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†—