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The company’s lead clinical-stage program, OLN324, is a higher potency, higher molar dose VEGF/Ang2 bispecific antibody currently in phase 1b clinical development for patients with either wAMD or DME.
Ollin Biosciences has announced its official launch, with an initial $100 million in financing led by ARCH Venture Partners, Mubadala Capital, and Monograph Capital.
The company states it is “assembling a robust pipeline of both clinical and late-stage preclinical programs, building upon validated biologies to better address unmet treatment needs in ophthalmology.”
Jason Ehrlich, MD, PhD, co-founder and CEO of Ollin, commented on the company’s official launch, saying, “Ollin is a purpose-built, asset-centric biotech with core expertise in ophthalmology drug development, bringing together a strong focus on operational execution, market-informed clinical development strategies, and cutting-edge data science and imaging tools. We believe our first bispecific programs present a tremendous opportunity to improve patient care with medicines that target more than one pathway, given the multi-factorial nature of many eye diseases.”
The company’s lead clinical-stage program, OLN324, is a higher potency, higher molar dose VEGF/Ang2 bispecific antibody currently in phase 1b clinical development for patients with either wet (neovascular) age-related macular degeneration (wAMD) or diabetic macular edema (DME). The company has completed enrollment of over 150 patients with wAMD or DME in the JADE study.
OLN324 is being tested at higher molar doses than faricimab for greater target coverage and the potential for extended treatment durability, according to the company.
The JADE study is a phase 1b proof-of-concept clinical trial, based in the US, designed to evaluate OLN324 versus faricimab for potential areas of anatomic and durability differentiation.
Charles C. Wykoff, MD, PhD, chairman of research at Retina Consultants of America, commented on the trial, saying, “Ollin’s Phase 1b study explores the potential for differentiation of OLN324 versus faricimab from the outset, indicating a strategy to leverage validated biologies and clear regulatory pathways to accelerate therapeutic development.”
Topline results from the study are expected in the first quarter of 2026.
An already completed single- and multiple-dose escalation phase 1 trial of OLN324 in DME conducted in China demonstrated “promising vision and anatomic improvements along with a favorable safety profile,” according to the company.
The company’s second program is OLN102, a first-in-class, TSHR/IGF-1R bispecific antibody for treatment of thyroid eye disease (TED), as well as the underlying autoimmune condition of Graves’ disease. The company notes that by inhibiting both the TSHR and IGF-1R receptors, OLN102 may offer TED patients improved safety and efficacy compared to existing medicines through more precise tissue targeting and a wider therapeutic index.
OLN102, discovered by and being developed in collaboration with VelaVigo, is expected to enter clinical development in 2026.
According to the company, it has assembled a “world-class team with proven success in end-to-end ophthalmic drug development and commercialization.” Furthermore, the company says its approach “integrates scientific insights with deep commercial market understanding and utilizes advanced ophthalmic image analysis tools to accelerate drug development and maximize therapeutic impact for patients.”
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