$330M Boost for Ollin Biosciences as It Preps Phase 3 Trials for Retinal Therapy

  • Ollin Biosciences raises $330M in oversubscribed Series B round led by TCGX and ARCH Venture Partners.
  • Proceeds will fund global Phase 3 trials for IBI324 (OLN324), a VEGF/Ang2 bispecific antibody targeting DME and wet AMD.
  • Phase 3 trials expected to begin in the second half of 2026, including sites in China and South Korea through Innovent partnership.
  • IBI324 showed faster retinal drying and greater vision gains compared to Vabysmo® in head-to-head JADE clinical trial.

Ollin Biosciences' significant Series B funding underscores investor confidence in the potential of IBI324 to challenge existing treatments for retinal vascular diseases. The $15 billion retina market is highly competitive, with established therapies like Vabysmo® and Eylea HD®. Ollin's ability to differentiate its product through superior clinical outcomes will be critical in capturing market share.

Clinical Trial Execution
The pace at which Ollin Biosciences can initiate and complete global Phase 3 trials for IBI324 will determine its competitive positioning in the $15 billion retina market.
Regulatory Approval Pathway
Whether the constructive feedback from FDA and EMA translates into a streamlined approval process for IBI324, potentially accelerating its market entry.
Commercialization Strategy
How Ollin Biosciences plans to leverage its strong investor syndicate to support the commercial launch of IBI324, particularly in key markets like China and South Korea.