- TUL said its UBT251 injection completed a Phase II study in China for type 2 diabetes, supporting plans to start a Phase III program.
- The company reported a maximum HbA1c reduction of 2.16% after 24 weeks in the UBT251 arms.
- It also reported a maximum average weight reduction of 9.8% over 24 weeks, compared with 4.8% for semaglutide 1 mg.
- TUL said UBT251 has been cleared to run clinical trials in China and/or the US across multiple metabolic indications, which could broaden its commercial scope.
- The company said it signed an exclusive licensing agreement with Novo Nordisk covering UBT251.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. TUL - The United Laboratories International Holdings Ltd. published the original content used to generate this news brief via IIS, the Issuer Information Service operated by the Hong Kong Stock Exchange (HKex) (Ref. ID: HKEX-EPS-20260325-12066073), on March 25, 2026, and is solely responsible for the information contained therein.
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