RBC Capital Markets Global Healthcare Conference 2026
Logotype for 4D Molecular Therapeutics Inc

4D Molecular Therapeutics (FDMT) RBC Capital Markets Global Healthcare Conference 2026 summary

Event summary combining transcript, slides, and related documents.

Logotype for 4D Molecular Therapeutics Inc

RBC Capital Markets Global Healthcare Conference 2026 summary

19 May, 2026

Strategic vision and market positioning

  • Aims to reset the retinal disease treatment paradigm with a lifelong, always-on gene therapy, moving away from frequent bolus injections for wet AMD and DME.

  • Sees a highly competitive and crowded market but believes its product profile is uniquely positioned for meaningful impact.

  • Differentiates from other gene therapies by offering intravitreal delivery, which is easier to integrate into clinical practice compared to surgical or subretinal approaches.

  • Expects its therapy to be considered for over 90% of AMD patients, except those well-controlled with minimal injections.

  • Projects the global anti-VEGF market could reach $20 billion as the population ages, with significant opportunity for backbone therapy.

Clinical development and regulatory outlook

  • Two pivotal Phase III studies for wet AMD are ongoing, with a pivotal DME trial planned to start in Q3, 2026.

  • Regulatory alignment achieved with FDA, EMA, and Japan for a single global DME trial, in partnership with Otsuka for Asia-Pacific.

  • Phase III trial designs are modeled after successful wet AMD studies, aiming for data that is both regulatory- and clinic-relevant.

  • Non-inferiority trials use strict rescue criteria, designed in collaboration with retina experts to ensure clinical relevance.

  • Upcoming catalysts include two-year PRISM follow-up data and DME SPECTRA trial updates in the second half of the year.

Commercial strategy and pricing

  • U.S. is the initial launch priority, but global approval is targeted with trials designed for broad adoption.

  • Partnership with Otsuka covers Asia-Pacific; European and other international markets are part of the long-term strategy.

  • Pricing will be well below the million-dollar range typical for rare disease gene therapies, likely under $100,000.

  • Manufacturing expertise and low dose requirements enable a cost of goods below $1,000, supporting competitive pricing.

  • Large, established patient populations and ongoing incidence rates support a sustainable business model without rare disease pricing.

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