Evaluation of HS-20137 in Chinese Patients with Moderate-to-Severe Psoriasis: Results from a Phase 2, Randomized, Double-Blind Trial - Summary - MDSpire

Evaluation of HS-20137 in Chinese Patients with Moderate-to-Severe Psoriasis: Results from a Phase 2, Randomized, Double-Blind Trial

  • By

  • Lin Cai

  • Xiaohua Wang

  • Litao Zhang

  • Guoqiang Zhang

  • Liming Wu

  • Baoqi Yang

  • Zudong Meng

  • Jihai Shi

  • Guangming Han

  • Aihua Wei

  • Shanshan Li

  • Yi Zhao

  • Juan Su

  • Nianjin Wei

  • Siying Liu

  • Ran Liu

  • Wei Liu

  • Min Fang

  • Xiaoqing Zhang

  • Jianzhong Zhang

  • March 22, 2026

  • 0 min

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Objective:

To evaluate the safety and efficacy of HS-20137, a monoclonal antibody targeting IL-23, over 52 weeks in Chinese patients with moderate-to-severe psoriasis.

Key Findings:
  • HS-20137 significantly improved psoriatic lesions and quality of life, with statistical significance.
  • The treatment demonstrated an excellent long-term therapeutic effect and safety profile, comparable to existing IL-23 therapies.
  • Findings support further development of HS-20137 as a competitive treatment option for psoriasis.
Interpretation:

HS-20137 shows promise as an effective treatment for moderate-to-severe psoriasis, with potential advantages over existing IL-23 therapies in terms of dosing frequency and safety.

Limitations:
  • The study did not perform a sample size estimation, which may affect the power of the results.
  • Results are based on a specific population (Chinese patients), which may limit generalizability to other populations.
  • Potential biases in participant selection and reporting may affect the findings.
Conclusion:

HS-20137 is a promising candidate for the treatment of moderate-to-severe psoriasis, warranting further investigation.

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