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Taking people in CanadaPhase 3

Testing sacituzumab tirumotecan with pembrolizumab in advanced lung cancer

Tests a drug combined with pembrolizumab against pembrolizumab alone in adults with advanced lung cancer.

Plain-language title generated from the registry record
Registry title: Sacituzumab Tirumotecan (MK-2870) in Combination With Pembrolizumab Versus Pembrolizumab Alone in Metastatic Non-small Cell Lung Cancer (NSCLC) With Programmed Cell Death Ligand 1 (PD-L1) Tumor Proportion Score (TPS) ≥ 50% (MK-2870-007)

Key facts

Where
Brampton, Mississauga, and Montreal, CanadaSee the 3 sites
Phase
Phase 3

Where in Canada

  • William Osler Health System (Site 0203)Brampton, CanadaTaking people
  • Trillium Health Partners - Credit Valley Hospital (Site 0202)Mississauga, CanadaTaking people
  • McGill University Health Centre (Site 0200)Montreal, CanadaNo longer taking part

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  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Merck Sharp & Dohme LLC
Trial code
NCT06170788EU 2023-503376-24-00
Record updated
3 November 2026
Original description
The primary objective of the study is to compare sacituzumab tirumotecan combined with pembrolizumab to pembrolizumab alone with respect to overall survival (OS). The primary hypothesis is that the combination of sacituzumab tirumotecan and pembrolizumab is superior to pembrolizumab alone with respect to OS.Read full original descriptionShow less

A Randomized, Open-label, Phase 3 Study of MK-2870 in Combination With Pembrolizumab Compared to Pembrolizumab Monotherapy in the First-line Treatment of Participants With Metastatic Non-small Cell Lung Cancer With PD-L1 TPS Greater Than or Equal to 50% (TroFuse-007)

The primary objective of the study is to compare sacituzumab tirumotecan combined with pembrolizumab to pembrolizumab alone with respect to overall survival (OS). The primary hypothesis is that the combination of sacituzumab tirumotecan and pembrolizumab is superior to pembrolizumab alone with respect to OS.

Inclusion: Histologically or cytologically confirmed diagnosis of squamous or nonsquamous NSCLC; Confirmation that epidermal growth factor receptor- (EGFR-), anaplastic lymphoma kinase- (ALK-), or proto-oncogene tyrosine-protein kinase ROS (ROS1-) directed therapy is not indicated as primary therapy; Provided tumor tissue that demonstrates programmed cell death ligand 1 (PD-L1) expression in ≥50% of tumor cells as assessed by an immunohistochemistry (IHC) central laboratory; An Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1 assessed within 7 days before randomization; A life expectancy of at least 3 months; Human immunodeficiency virus (HIV)-infected participants must have well controlled HIV on antiretroviral therapy (ART).

Exclusion: Has active inflammatory bowel disease requiring immunosuppressive medication or previous clear history of inflammatory bowel disease (eg, Crohn's disease, ulcerative colitis, or chronic diarrhea); Received prior systemic anticancer therapy for their metastatic NSCLC; Received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent, or with an agent directed to another stimulatory or coinhibitory T-cell receptor Note: Prior treatment with an anti-PD-1, anti-PD- L1, or anti-PD-L2 agent in the neoadjuvant or adjuvant setting for nonmetastatic resectable NSCLC is allowed as long as therapy was completed at least 12 months before diagnosis of metastatic NSCLC; Received prior systemic anticancer therapy including investigational agents within 4 weeks before randomization; Received radiation therapy to the lung that is >30 Gy within 6 months of start of study intervention; Received prior radiotherapy within 2 weeks of start of study intervention, or radiation-related toxicities, requiring corticosteroids; Received a live or live-attenuated vaccine within 30 days before the first dose of study intervention. Administration of killed vaccines are allowed; Diagnosis of immunodeficiency or is receiving chronic systemic steroid therapy; Concurrent active Hepatitis B and Hepatitis C virus infection; Requires treatment with a strong inhibitor or inducer of Cytochrome P450 3A4 (CYP3A4) at least 14 days before the first dose of study intervention and throughout the study; Diagnosis of small cell lung cancer or, for mixed tumors, presence of small cell elements; History of documented severe dry eye syndrome, severe Meibomian gland disease and/or blepharitis, or severe corneal disease that prevents/delays corneal healing; Has uncontrolled, significant cardiovascular disease or cerebrovascular disease within the 6 months preceding study intervention; Known additional malignancy that is progressing or has required active treatment within the past 3 years; Known intolerance to sacituzumab tirumotecan or pembrolizumab and/or any of their excipients; for pembrolizumab, severe hypersensitivity (≥Grade 3) is exclusionary; Known hypersensitivity to sacituzumab tirumotecan or other biologic therapy; Active autoimmune disease that has required systemic treatment in the past 2 years; History of (noninfectious) pneumonitis/interstitial lung disease (ILD) that required steroids or has current pneumonitis/ILD; Active infection requiring systemic therapy; Human immunodeficiency virus (HIV)-infected participants with a history of Kaposi's sarcoma and/or Multicentric Castleman's Disease; History of allogeneic tissue/solid organ transplant; Has Grade ≥2 peripheral neuropathy; Known active central nervous system (CNS) metastases and/or carcinomatous meningitis.

ClinicalTrials.gov NCT06170788 · EU CTIS 2023-503376-24-00