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Chia Tai Tianqing's TQB2102 Doubles Progression-Free Survival in HER2-Low Breast Cancer Phase III

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Chia Tai Tianqing, a core subsidiary of Sino Biopharmaceutical, has reported pivotal Phase III results for its independently developed HER2-directed antibody-drug conjugate TQB2102 in HER2-low breast cancer, selected as a late-breaking abstract for a proffered paper session at ESMO. The trial showed a median progression-free survival of 16.4 months with TQB2102 versus 5.5 months with comparator chemotherapy, an approximately 71% reduction in the risk of disease progression or death, and a 2.2% incidence of treatment-related ILD. The data position TQB2102 as a potential competitor in a field where trastuzumab deruxtecan has set the benchmark, though questions of full survival data, regulatory filing timelines, and comparative efficacy remain open.

Written by a model from the reports · updated 2 hours ago

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Oct 23
  1. mp.weixin.qq.comPick
    Chia Tai Tianqing Reports Phase III Results for TQB2102 in HER2-Low Breast Cancer at ESMO

    Chia Tai Tianqing, a core subsidiary of Sino Biopharmaceutical, reported pivotal Phase III results for its independently developed TQB2102 in HER2-low breast cancer, selected as a late-breaking abstract for a proffered paper session at ESMO. The abstract showed a median progression-free survival of 16.4 months with TQB2102 versus 5.5 months with comparator chemotherapy, an approximately 71% reduction in risk of disease progression or death, and a 2.2% incidence of treatment-related ILD.

  2. mp.weixin.qq.com
    Chia Tian Qing's TQB2102 Succeeds in Late-Stage HER2-Low Breast Cancer Study, mPFS 16.4 Months

    Chia Tian Qing's TQB2102 met its endpoint in a late-stage study in HER2-low breast cancer, with a median progression-free survival of 16.4 months versus 5.5 months in the chemotherapy control group. The risk of disease progression or death fell by about 71%, and treatment-related interstitial lung disease occurred in 2.2% of patients. Results were presented at the 2026 ESMO annual meeting.

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