Sac-TMT

Drug

Drug Profile

Sac-TMT (sacituzumab tirumotecan; also known as SKB264/MK-2870) is a human TROP2-directed antibody-drug conjugate targeting advanced solid tumors. Corporate regulatory disclosures report four approved and marketed indications in China and ongoing global Phase 3 development programs led by MSD. The ADC delivers a belotecan-derivative topoisomerase I inhibitor payload after TROP2-mediated internalization.

Drug Class
TROP2-directed antibody-drug conjugate (ADC)
Approval Status
Approved and marketed by NMPA in China for four indications; ongoing global Phase 3 development outside Greater China
Mechanism of Action
Anti-TROP2 antibody-drug conjugate that binds TROP2, is endocytosed, and releases a belotecan-derivative topoisomerase I inhibitor payload (KL610023) causing DNA damage, cell-cycle arrest, and apoptosis.
Indications
  • \EGFR-mutant locally advanced or metastatic non-squamous NSCLC after progression on EGFR-TKI therapy and platinum-based chemotherapy\
  • \Unresectable locally advanced or metastatic triple-negative breast cancer after at least two prior systemic therapies\
  • \EGFR-mutant locally advanced or metastatic non-squamous NSCLC after progression on EGFR-TKI therapy\
  • \Unresectable or metastatic HR+/HER2- breast cancer after prior endocrine therapy and at least one line of chemotherapy in advanced setting\

Related News

Novel ADC Shows Significant Survival Benefit in Pretreated EGFR-Mutated NSCLC

The antibody-drug conjugate sacituzumab tirumotecan demonstrated significant survival benefits in pretreated EGFR-mutated NSCLC, with median overall survival of 20.0 months versus 13.5 months for docetaxel. The treatment also showed superior progression-free survival and objective response rates with a favorable safety profile compared to chemotherapy.

Sac-TMT Shows Significant Survival Benefit in Pretreated EGFR-Mutated NSCLC

Sacituzumab tirumotecan demonstrated a median overall survival of 20.0 months versus 13.5 months with docetaxel in pretreated EGFR-mutated NSCLC patients. The phase 2 OptiTROP-Lung03 study showed a hazard ratio of 0.63 for overall survival benefit with the TROP2-directed antibody-drug conjugate.

Related Clinical Trials

NCT ID Title Status Phase
NCT07077564

The Efficacy of TROP2-ADC in Advanced Extrapulmonary High-Grade Neuroendocrine Neoplasms Failure of Standard Therapy

NOT_YET_RECRUITING PHASE2
NCT06422143

Pembrolizumab With or Without Maintenance Sacituzumab Tirumotecan (Sac-TMT; MK-2870) in Metastatic Squamous Non-small Cell Lung Cancer (NSCLC) [MK-2870-023]

RECRUITING PHASE3