U.S., Aug. 8 -- ClinicalTrials.gov registry received information related to the study (NCT07109284) titled 'SKB264 Combined With KL-A167 Neoadjuvant Therapy for Early-stage, High-risk ER+/HER2- Breast Cancer' on July 31.
Brief Summary: This study aimed to evaluate the efficacy and safety of SKB264 combined with KL-A167 as neoadjuvant therapy in early-stage high-risk ER+HER2- breast cancer patients.
Study Start Date: Sept., 2025
Study Type: INTERVENTIONAL
Condition:
ER+HER2- Breast Cancer
Intervention:
BIOLOGICAL: Sacituzumab tirumotecan
Sacituzumab tirumotecan 5 mg/kg, intravenously (iv), Q2W
BIOLOGICAL: Tagitanlimab
Tagitanlimab 900mg, intravenously (iv), Q2W
Recruitment Status: NOT_YET_RECRUITING
Sponsor: West China Hospital
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