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NCT07258108PHASE2RECRUITING

Sac-TMT Plus KL-A167 in PD-L1+, HR+/HER2- Metastatic Breast Cancer After CDK4/6 Inhibitors

A Phase II Study of Sacituzumab Tirumotecan (Sac-TMT) Combined With Tagitanlimab(KL-A167) in PD-L1-Positive, Hormone Receptor-Positive/HER2-Negative Metastatic Breast Cancer Patients Previously Treated With CDK4/6 Inhibitors

Sponsor: Sun Yat-sen University + Fifth Affiliated Hospital, Sun Yat-Sen University

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Key Facts

Study type
INTERVENTIONAL
Conditions
Breast Cancer
Interventions
Lucanisatuzumab plus tagolimumab
Enrollment
35 participants
Primary completion
Jul 2027
Study completion
Dec 2028
First posted
Dec 2025
Last updated
May 2026

Primary Endpoints (CT.gov)

6-month progression-free survival rate (PFS)

Time frame: 6 months

Secondary Endpoints

Objective Response Rate (ORR)

Progression-Free Survival (PFS)

Disease Control Rate (DCR)

Eligibility Criteria

Inclusion Criteria: 1. 18-75 years old. 2. HR+/HER2- breast cancer (BC), meeting the following conditions: 1. HR+/HER2-; HER2-(IHC 0 or 1+); IHC 2+(FISH negative); HR+ (ER and/or PR IHC showed ≥1%); 2. Tumor stage: Locally advanced, recurrent, or metastatic HR+/HER2- breast cancer; 3) Disease progression during or within 12 months after completion of adjuvant endocrine therapy based on a CDK4/6 inhibitor, or disease progression on CDK4/6 inhibitor treatment for metastatic disease; 4) PD-L1 positive (CPS ≥ 1); 5) At least one measurable target lesion as assessed by the investigator per RECIST 1.1; 6) Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1; Life expectancy more than 12 weeks; 7) Adequate organ function, defined as: <!-- --> 1. Complete blood count: Neutrophil count ≥ 1.5×10\^9/L; platelets ≥ 100×10\^9/L; hemoglobin ≥ 9 g/dL. 2. Liver function: AST, ALT, and ALP ≤ 2.5× ULN; total bilirubin ≤ 1.5× ULN; ALT and AST ≤ 5× ULN, TBIL ≤ 2×

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✦ Analyst Commentary

Expert commentary on why this trial matters and what to watch for.

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Source

Open on ClinicalTrials.gov