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NeoCARD: Anthracycline-Free Neoadjuvant Chemoimmunotherapy in Triple-Negative Breast Cancer Patients

Study acronym: NeoCARD
StatusRecruiting
PhasePhase 2
Started
View on ClinicalTrials.gov ↗

Record History

  1. Minor Eligibility criteria expanded, about 290 words Study description shortened, about 357 words · Study title revisedv7 Show 2 more changesShow less
    • Study description shortened, about 357 words
    • Study title revised

    See this version in full on ClinicalTrials.gov ↗

  2. Notable Trial status: Not Yet Recruiting to Recruiting Study sites: 0 to 1 · Primary completion date: Jun 30, 2027 to Oct 20, 2027 · Completion date: Jun 30, 2028 to Oct 20, 2028 · 2 morev6 Show 5 more changesShow less
    • Study sites: 0 to 1
    • Primary completion date: Jun 30, 2027 to Oct 20, 2027
    • Completion date: Jun 30, 2028 to Oct 20, 2028
    • Start date changed from estimate of Nov 1, 2025 to Oct 20, 2025
    • Eligibility criteria expanded, about 111 words

    See this version in full on ClinicalTrials.gov ↗

  3. Notable Start date: Aug 1, 2025 to Nov 1, 2025v5
  4. Notable Start date: Jul 1, 2025 to Aug 1, 2025v4
  5. Notable Start date: Jun 1, 2025 to Jul 1, 2025v3
  6. Minor Re-verified, no change to tracked fieldsv2
  7. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This is a single-arm Phase II study to assess the efficacy of a 12-18 week neoadjuvant carboplatin, paclitaxel, and pembrolizumab (CPP) regimen in a response-adaptive manner for triple-negative breast cancer (TNBC) patients who are ineligible for anthracycline-based therapy due to underlying cardiac conditions.
Trial Details
NCT Number NCT06845319
Lead Sponsor Medical University of South Carolina
Conditions Triple Negative Breast Cancer
Enrollment 43 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov