HANSOH PHARMA Receives NMPA Breakthrough Therapy Designation for HS-20093-Adebrelimab Combo in Advanced NSCLC

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Hansoh Pharmaceutical Group Company Limited (HANSOH PHARMA) announced that China’s National Medical Products Administration (NMPA) has granted Breakthrough-Therapy designation to the company’s self-developed B7-H3-targeted antibody-drug conjugate (ADC) HS-20093 when used in combination with adebrelimab.

According to the April 16 2026 filing, the proposed indication covers patients with locally advanced or metastatic non-squamous non-small cell lung cancer (NSCLC) lacking actionable genomic alterations whose disease has progressed or relapsed following platinum-based chemotherapy.

The designation is expected to expedite clinical development and review timelines for HS-20093 plus adebrelimab, reflecting unmet medical need in this patient segment.

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