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Zea’s Lead Drug Program:  Hemophilia B Tolerization







               Program Highlights:




               • Roughly a $250M/year opportunity                                                                 License IP
                    (We estimate 85% market share)                                                    Platform  Lighthouse
                                                                                                             Qualif.
                                                                                                         ID Lyo + QC vendors         Lyo   GMP    Lyo

               • Drug Program estimated buyout:  $25M                                                       QC                                    Acute Tox
                                                                                                      Hemophilia B / UPenn  Draft Docs
                                                                                                                                                          GMP Release

                                                                                                                            Protocols
               • Time for development:  18-24 months                                                                   ID CROs; Contracts                    Dose Range   6m+PK/BD



               • Significantly de-risked program since                                                               Request   Brief  Pre-IND                                 IND
                    majority of R&D was developed                                                              2023                                            2024





                  Competitive Landscape:



                  • Only one therapy available:

                       (Costing over $1M+ year/patient)



                  • Not always effective
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