๐๏ธ Verified NIH Record โข Updated 2025-02-25
Neoadjuvant Carboplatin and Docetaxel in Triple Negative Breast Cancer (NCT02547987)
CADENCE: Carboplatin and Docetaxel in Neoadjuvant Treatment of ER-Negative, HER2-Negative Breast Cancer: A Co-Clinical Trial With Genoproteomic Discovery
๐ต Active, Not Recruiting Phase2 ๐ Investigational Drug / Biologic Sponsor: Mothaffar Rimawi
๐ฉบ Plain-English Summary (8th-Grade Level)
The purpose of this study is to determine whether the combination of docetaxel and carboplatin is an effective treatment for patients with triple negative breast cancer.
Who can join: Review the eligibility criteria below.
Location: TriHealth Hatton Research โ Cincinnati, Ohio
Age range: 18 Years
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (3 Sites)
- TriHealth Hatton Research โ Cincinnati, Ohio
- Lester & Sue Smith Breast Center at Baylor College of Medicine โ Houston, Texas
- Harris Health System Smith Clinic โ Houston, Texas
๐ฐ 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.
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๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Review the official NIH record below to find the coordinating site.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.