4D Molecular Therapeutics Secures $85 Million Upfront in Strategic AAV Partnership with Otsuka for Retinal Diseases

Oct 30 , 2025
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EMERYVILLE, Calif. — 4D Molecular Therapeutics (4DMT), a late-stage biotechnology company specializing in AAV genetic medicine, today announced a strategic partnership with Otsuka Pharmaceutical Co., Ltd. to develop and commercialize 4D-150 for the treatment of wet age-related macular degeneration (wet AMD) and diabetic macular edema (DME) across the greater Asia-Pacific (APAC) region.

The collaboration leverages 4DMT’s expertise in AAV vector design—specifically the R100 vector used in 4D-150—and combines it with Otsuka’s robust development, regulatory, and commercial infrastructure in APAC markets. 4D-150 is designed as a potentially transformative backbone therapy aimed at providing durable, multi-year anti-VEGF delivery from the retina via a single, safe, intravitreal injection, potentially freeing patients from burdensome, frequent injections.

Financial and Clinical Details:

  • 4DMT will receive an $85 million upfront cash payment.
  • The partnership includes expected cost sharing of at least $50 million from Otsuka over the next three years for global development activities, supporting the global Phase 3 clinical trial in DME and pre-commercial activities.
  • 4DMT is eligible for up to $336 million in potential regulatory and commercial milestone payments, plus tiered double-digit royalties on net sales in Otsuka’s territories.
  • 4DMT retains full development and commercialization rights outside of APAC, including the U.S. and Europe, and will continue to lead all Phase 3 clinical activities globally.

The companies aim to accelerate the global registration of 4D-150 to address wet AMD and DME, which are leading causes of blindness worldwide.

Source:

https://ir.4dmoleculartherapeutics.com/news-releases/news-release-details/4dmt-announces-exclusive-license-agreement-otsuka-pharmaceutical

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PackGene Biotech is a world-leading CRO and CDMO, excelling in AAV vectors, mRNA, plasmid DNA, and lentiviral vector solutions. Our comprehensive offerings span from vector design and construction to AAV, lentivirus, and mRNA services. With a sharp focus on early-stage drug discovery, preclinical development, and cell and gene therapy trials, we deliver cost-effective, dependable, and scalable production solutions. Leveraging our groundbreaking π-alpha 293 AAV high-yield platform, we amplify AAV production by up to 10-fold, yielding up to 1e+17vg per batch to meet diverse commercial and clinical project needs. Moreover, our tailored mRNA and LNP products and services cater to every stage of drug and vaccine development, from research to GMP production, providing a seamless, end-to-end solution.

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