Boehringer Ingelheim and Re-Vana Therapeutics announced a strategic collaboration effort focused on advancing developments for extended-release therapies of eye-diseases. The collaboration pairs Re-Vana’s extended-release platform with Bohringer’s renown research and development process.
Key Takeaways
- The collaboration aims to pair Boehringer Ingelheim’s renown R&D with Re-Vana’s innovative limited injection therapy treatment.
- Boehringer will implement Re-Vana’s drug delivery technology into its pipeline.
- The deal is valued to be upwards of $1 billion with factors dependent on project developments and outstanding royalty fees.
Michael O’Rourke, Re-Vana’s chief executive officer, touched on the impact of the collaboration, saying, “The strategic collaboration with Boehringer Ingelheim marks a transformational moment for Re-Vana. By combining our extended-release platform with Boehringer Ingelheim’s world-class research and development capabilities and eye health pipeline, we strive to bring forward a new generation of long-acting treatments for eye diseases that offer clinical and quality-of-life benefits for patients.” 1
More than meets the eye
Boehringer Ingelheim leads the industry as one of the top investors in research and development for therapies that improve and extend the lives of those in communities struggling with medical care. Boehringer employs its research directly into its diverse pipeline of eye health products including its four Phase 2 testing assets, and the commitment to preserving patient’s retinas. Boehringer believes that preserving the retina can protect a patient’s way of life and prevent vision loss.
Accompanying these beliefs and executions is Queen’s University Belfast spin-out Re-Vana, an ocular therapeutics and innovative ocular drug delivery company. Re-Vana’s ophthalmic disease treatment looks to change the way patients administer treatments by reducing the frequency of injections patients must make directly into their eyes. The drug delivery method is designed to slowly release treatments over the span of six to twelve months providing patients with the benefit of reduced injections.