复星医药(600196.SH)控股子公司药品获美国FDA注册批准
智通财经网·2025-11-14 10:18

Core Viewpoint - Fosun Pharma's subsidiary, Shanghai Fuhong Hanlin Biotechnology Co., Ltd., received FDA approval for its self-developed injectable drug POHERDY®1 (HLX11), indicating a significant advancement in the treatment of HER2-positive metastatic breast cancer [1] Group 1: FDA Approval Details - The FDA approved the biologics license application (BLA) for POHERDY®1, which is an injectable solution for intravenous use [1] - The approved indications include treatment for adult patients with HER2-positive metastatic breast cancer who have not previously received anti-HER2 therapy or chemotherapy [1] - The drug is also indicated for use in combination with trastuzumab and chemotherapy for early-stage breast cancer as part of a comprehensive treatment plan [1] Group 2: Treatment Applications - POHERDY®1 is indicated for neoadjuvant treatment in adult patients with HER2-positive locally advanced, inflammatory, or early breast cancer [1] - It is also approved for adjuvant treatment in adult patients with HER2-positive early breast cancer who are at high risk of recurrence [1]