NovaBridge Biosciences
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NovaBridge Biosciences (NBP) investor relations material

NovaBridge Biosciences H.C. Wainwright 28th Annual Global Investment Conference summary

Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
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H.C. Wainwright 28th Annual Global Investment Conference summary14 Sep, 2026

Strategic overview and business model

  • Focuses on sourcing late-stage assets, primarily from Asia, with proven phase I/II data and advancing them through a flexible capital allocation framework.

  • Aims to repeatedly identify, de-risk, and develop differentiated therapeutics for global markets, leveraging a U.S.-based clinical team and Nasdaq listing.

  • Seeks assets with established mechanisms of action, clear differentiation, and unmet needs, prioritizing those already de-risked in early clinical trials.

  • Explores opportunities to bypass the U.S. market, targeting Europe and APAC, and is particularly interested in underappreciated areas like women's health.

  • Employs a hub-and-spoke model to develop, partner, or finance assets, adapting strategy based on market and asset specifics.

Givastomig clinical development and differentiation

  • Givastomig is a bispecific antibody targeting claudin 18.2 and 4-1BB, conditionally activated in tumors, showing efficacy in low claudin expressers.

  • Phase I data demonstrated activity at both 8 mg and 12 mg doses, with improved response rates and median PFS over standard of care.

  • FDA feedback supports moving directly to phase III, with ongoing dose selection balancing efficacy, safety, and tolerability.

  • The molecule's design allows for a broader addressable market, potentially doubling eligible patients, especially in HER2-negative gastric cancer.

  • Expansion into pancreatic and biliary tract cancers is underway, with results expected over the next year to validate the platform beyond gastric cancer.

VIS-101 and ophthalmology pipeline

  • VIS-101 is a bispecific peptide body targeting VEGF and Ang2, designed for neovascular AMD, with differentiation driven by durability and reduced retreatment rates.

  • Phase II-A showed promising efficacy and durability; phase II-B is scaling up with a 100-patient trigger for phase III, in partnership with Everest Medicines.

  • Phase III design aims to demonstrate both efficacy and extended treatment intervals versus standard of care, without trade-offs.

  • Visara, the majority-owned subsidiary, is expanding its pipeline to include front-of-the-eye assets, such as VIS-102 for neurotrophic keratitis, focusing on patient convenience and differentiation.

  • Innovation includes developing assets that do not require cold chain logistics, addressing significant patient and caregiver burdens.

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