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Kelun-Biotech Presents First-in-human Study Data for Its Novel B7-H3 ADC SKB500 at ASCO 2026

Kelun-Biotech said the drug showed a manageable safety profile and early anti-tumor activity in 140 patients across dose levels.

  • On Tuesday, June 2, 2026, Kelun-Biotech presented first-in-human study results for the B7-H3 ADC SKB500 at the American Society of Clinical Oncology Annual Meeting in Chicago.
  • Professor Liu Haifeng from Jilin Provincial Cancer Hospital presented the findings as a rapid oral report, detailing how SKB500 targets advanced solid tumors, a major area of unmet medical need.
  • Clinical results showed broad-spectrum anti-tumor activity, with patients receiving the 12 mg/kg dose exhibiting a more favorable safety profile than the 16 mg/kg group, demonstrating robust efficacy and manageable safety.
  • Among treated extensive-stage small cell lung cancer patients, the objective response rate reached 54.1%, with investigators noting a low rate of permanent treatment discontinuation, laying a solid foundation for further clinical development.
  • Representing one of several drug projects, SKB500 aligns with Kelun-Biotech's commitment to becoming a leading global enterprise and addressing critical gaps in cancer treatment.
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Kelun-Biotech Presents First-in-human Study Data for Its Novel B7-H3 ADC SKB500 at ASCO 2026

CHENGDU, China, June 2, 2026 /PRNewswire/ -- Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd. ("Kelun-Biotech" or the "Company", 6990.HK) announced that at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting held in Chicago, USA, the first-in-human study results of the…

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PR Newswire broke the news in United States on Wednesday, June 3, 2026.
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