A Clinical Study of Sacituzumab Tirumotecan (Sac-TMT, MK-2870) in People With Breast Cancer (MK-2870-032)

NCT06966700Phase 3Recruiting

Lead sponsor
Merck Sharp & Dohme LLC (Industry)
Enrollment
2,400 (estimated)
Start date
30 Jun 2025
Primary completion
23 Mar 2033 (estimated)
Study completion
29 Dec 2034
Last update posted
13 Oct 2026

Design

Study type
Interventional
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel
Masking
None
Arms
2

Interventions

  • Sacituzumab tirumotecan Biological
  • Pembrolizumab Biological
  • Rescue Medication Drug
  • Carboplatin Drug
  • Paclitaxel Drug
  • Doxorubicin Drug
  • Epirubicin Drug
  • Cyclophosphamide Drug
  • Capecitabine Drug
  • Olaparib Drug

Conditions and primary outcome

  • Breast Neoplasms
  • Triple Negative Breast Neoplasms
  • HR Low-Positive/HER2-Negative Breast Neoplasms

Primary outcome

Percentage of Participants with Pathological Complete Response (pCR) at the Time of Definitive Surgery (Up to approximately 30 weeks); Event-Free Survival (EFS) (Up to approximately 92 months)

Posted results on ClinicalTrials.gov

Results posted on ClinicalTrials.gov: No

Results from company and journal sources

No editor-confirmed results are on record for this study.

Publications

1 on PubMed
  1. TroFuse-032 study design: pembrolizumab plus sacituzumab tirumotecan or chemotherapy followed by pembrolizumab plus chemotherapy as neoadjuvant therapy for early-stage, triple-negative breast cancer or HR-low+/HER2- breast cancer.

    Future oncology (London, England) · 2026 Oct 14

Citations from PubMed, U.S. National Library of Medicine; abstracts are not stored. A publication lists this study’s NCT number and may be a review that cites many studies.

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Data integrity

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Source

Source: ClinicalTrials.gov, U.S. National Library of Medicine. Listing a study does not mean NLM has evaluated it.

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