๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-06-03

Palbociclib With Fulvestrant for Metastatic Breast Cancer After Treatment With Palbociclib and an Aromatase Inhibitor (NCT02738866)

Phase II Trial of Palbociclib With Fulvestrant in Individuals With Hormone Receptor-Positive, HER2-Negative Metastatic Breast Cancer Who Have Progressed on Treatment With Palbociclib and an Aromatase Inhibitor

๐Ÿ”ต Active, Not Recruiting Phase2 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

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

This study is being done to look at the role of continuing palbociclib treatment in combination with another type of hormonal therapy (fulvestrant) after disease progression of palbociclib in combination with an aromatase inhibitor.

Who can join: Review the eligibility criteria below.

Location: Kimmel Cancer Center at Johns Hopkins at Sibley Memorial Hospital โ€” Washington D.C., District of Columbia

Age range: 18 Years

๐Ÿงช Interventions in This Study

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)

  • Kimmel Cancer Center at Johns Hopkins at Sibley Memorial Hospital โ€” Washington D.C., District of Columbia
  • Anne Arundel Health System Research Institute, Inc. โ€” Annapolis, Maryland
  • Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins โ€” Baltimore, Maryland
  • Allegheny Health Network (AHN) - Allegheny General Hospital ONLY โ€” Pittsburgh, Pennsylvania
  • Reading Hospital - McGlinn Cancer Institute โ€” West Reading, Pennsylvania

๐Ÿ“ž Contact the Study Coordinator

Phone: (855) 694-6725

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†—