Logotype for 4D Molecular Therapeutics Inc

4D Molecular Therapeutics (FDMT) Corporate presentation summary

Event summary combining transcript, slides, and related documents.

Logotype for 4D Molecular Therapeutics Inc

Corporate presentation summary

14 Aug, 2026

Strategic focus and innovation

  • Advancing a pipeline of next-generation, locally delivered AAV genetic medicines targeting large market diseases, with 4D-150 as the lead product for retinal vascular diseases and 4D-710 for cystic fibrosis lung disease.

  • Emphasizing broad commercial adoption through simple delivery, best-in-class safety, low cost of goods, and global regulatory alignment.

  • Commercial model designed for scalability, efficient infrastructure, and favorable economics for payers and clinics.

4D-150 for retinal vascular diseases

  • 4D-150 aims to transform care for wet AMD and DME with a single, durable, in-office injection, reducing treatment burden by up to 87% over two years.

  • Demonstrated stable visual acuity and anatomy with robust reduction in supplemental anti-VEGF injections across severe, broad, and recently diagnosed populations.

  • Consistent and predictable safety profile with no serious adverse events related to 4D-150.

  • Global Phase 3 trials (4FRONT-1 and 4FRONT-2) fully enrolled, targeting noninferiority to aflibercept and regulatory alignment in the US, EU, and Japan.

  • Exclusive APAC commercialization partnership with Otsuka, including $85M upfront, cost sharing, and milestone payments.

4D-710 for cystic fibrosis lung disease

  • 4D-710 is a durable, redosable, variant-agnostic gene therapy delivered via aerosol for CF lung disease, addressing high unmet need in patients ineligible or intolerant to CFTR modulators.

  • Demonstrated dose-dependent, durable CFTR expression in airway cells, with the selected Phase 2 dose meeting target expression and safety profiles.

  • Clinically meaningful improvements in lung function (ppFEV1, LCI 2.5) and quality of life (CFQ-R-R) observed through at least one year.

  • Well-tolerated with only mild, transient adverse events and no pulmonary AEs after day 14.

  • Phase 2 enrollment underway, with further biomarker and clinical endpoint integration to demonstrate mechanism and activity.

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