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

Event summary combining transcript, slides, and related documents.

Logotype for NovaBridge Biosciences

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

14 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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