🏛️ Verified NIH Record • Updated 2026-06-11

Trastuzumab Deruxtecan (T-DXd) in Patients Who Have Hormone Receptor-negative and Hormone Receptor-positive HER2-low or HER2 IHC 0 Metastatic Breast Cancer (NCT05950945)

A Phase 3b, Multicenter, Global, Interventional, Open-label Study of Trastuzumab Deruxtecan (T-DXd), an Anti-HER2-Antibody Drug Conjugate (ADC), in Subjects Who Have Unresectable and/or Metastatic HER2-low or HER2 Immunohistochemistry (IHC) 0 Breast Cancer (DESTINY-Breast15)

🟢 Recruiting Phase3 💊 Investigational Drug / Biologic Sponsor: Daiichi Sankyo

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

This study will evaluate the safety and efficacy of trastuzumab deruxtecan (T-DXd) in participants with human epidermal growth factor receptor 2 (HER2)-low or HER2 immunohistochemistry (IHC) 0 (who are both hormone receptor \[HR\]-negative and HR-positive) unresectable and/or metastatic breast cancer.

Who can join: Review the eligibility criteria below.

Location: Mount Sinai Medical Center — Miami Beach, Florida

Age range: 18 Years

🧪 Interventions in This Study

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (88 Sites)

Showing the first 25 of 88 sites.

  • Mount Sinai Medical Center — Miami Beach, Florida
  • USF College of Medicine — Tampa, Florida
  • Dana-Farber Cancer Institute — Boston, Massachusetts
  • Beth Israel Lahey Health — Burlington, Massachusetts
  • Overlook Medical Center — Summit, New Jersey
  • Mater Hospital Sydney — North Sydney, New South Wales
  • Monash Medical Centre Moorabbin — East Bentleigh, Victoria
  • GenesisCare St Andrews Hospital — Adelaide,
  • Fiona Stanley Hospital — Murdoch,
  • Institut Jules Bordet — Anderlecht,
  • GZA Ziekenhuizen — Antwerp,
  • Universitair Ziekenhuis Brussel — Brussels,
  • Cliniques Universitaires Saint-Luc — Brussels,
  • UZ Leuven — Leuven,
  • Centre Hospitalier Universitaire de Liege Sart-Tilman — Liège,
  • GZA Ziekenhuizen — Wilrijk,
  • Centro de Oncologia - Unidade Brasília - Hospital Sírio Libanês — Brasília,
  • CIONC-Centro Integrado de Oncologia de Curitiba — Curitiba,
  • Hospital Erasto Gaertner - Liga Paranaense de Combate ao Câncer — Curitiba,
  • CEPON - Centro de Pesquisas Oncológicas de Santa Catarina — Florianópolis,
  • Oncosite - Centro de Pesquisa Clinica e Oncologia — Ijuí,
  • Fundação Doutor Amaral Carvalho — Jaú,
  • Instituto de Cancer de Londrina — Londrina,
  • Hospital das Clínicas FMRP-USP — Riberão Preto,
  • Hospital Nossa Senhora da Conceicao — Rio Grande,

📞 Contact the Study Coordinator

Phone: (908) 992-6400

Email: CTRinfo@dsi.com

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

💰 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 § 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

💡 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.
🏛️ View Official NIH Record ↗