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Harbour BioMed Reports the Online Publication of Phase I Results for HBM9378 (SKB378/WIN378), a TSLP-Targeting Antibody
Phase I trial showed HBM9378’s long half-life of 55 to 66 days and low immunogenicity in 50 healthy adults, supporting its use for asthma and COPD treatment.
- Harbour BioMed published online on March 22, 2026, the Phase I trial results of HBM9378 led by Dr. Min Xu in a peer‑reviewed journal.
- HBM9378 is a half‑life‑extended anti‑TSLP antibody engineered for half‑life extension and silenced effector function, co‑developed by Harbour BioMed and Kelun‑Biotech to treat asthma and chronic obstructive pulmonary disease .
- In the Phase I study, investigators enrolled 50 healthy adult subjects across three dose cohorts, with a 5% ADA incidence and no injection-site reactions, showing Tmax 4.05–14.1 days and half-life 55.0–65.8 days.
- Harbour BioMed and Kelun‑Biotech granted Windward Bio AG the global rights outside Greater China; the NMPA approved an IND in China, and the program has advanced to global testing.
- The positive Phase I results for HBM9378 mark a significant milestone in our mission to develop innovative therapies for immunological diseases, said Dr. Jingsong Wang, Founder, Chairman, and CEO of Harbour BioMed.
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Harbour BioMed Reports the Online Publication of Phase I Results for HBM9378 (SKB378/WIN378), a TSLP-Targeting Antibody
CAMBRIDGE, Mass., ROTTERDAM, Netherlands and SHANGHAI, March 22, 2026 /PRNewswire/ -- Harbour BioMed (HKEX: 02142, the "Company"), a global biopharmaceutical company committed to the discovery and development of novel antibody therapeutics focusing on immunology and immune-oncology, today announced the online…
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Total News Sources27
Leaning Left3Leaning Right4Center13Last UpdatedBias Distribution65% Center
Bias Distribution
- 65% of the sources are Center
65% Center
15%
C 65%
R 20%
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