
Opus Genetics
A gene therapy company for ultra-rare blinding conditions.
Date | Investors | Amount | Round |
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investor investor investor | €0.0 | round | |
investor | €0.0 Valuation: €0.0 | round | |
investor | €0.0 | round | |
investor | €0.0 | round | |
investor investor investor investor | €0.0 | round | |
* | $2.0m | Grant | |
Total Funding | 000k |
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Opus Genetics is a pioneering biotech startup focused on developing gene therapies for rare inherited retinal diseases (IRDs). These are genetic disorders that cause vision loss and blindness. The company is dedicated to creating advanced treatments that target specific genetic mutations responsible for these conditions.
Opus Genetics primarily serves patients suffering from rare eye diseases, a niche but critical segment of the healthcare market. The company operates in the biotechnology and gene therapy sector, which is a rapidly growing field aimed at treating genetic disorders at their root cause by altering or replacing defective genes.
The business model of Opus Genetics revolves around research and development (R&D) of gene therapies. They are backed by the Retinal Degeneration Fund, the venture arm of the Foundation Fighting Blindness. This backing provides them with both financial support and invaluable insights into patient needs. By focusing on wholly owned programs, Opus Genetics maintains control over their research and development processes, ensuring that their therapies are tailored specifically to the needs of patients with rare retinal diseases.
Opus Genetics makes money through a combination of funding from venture capital, grants, and potentially future revenue from the commercialization of their gene therapies. As their treatments progress through clinical trials and receive regulatory approval, they can be marketed and sold to healthcare providers and directly to patients, generating revenue.
In summary, Opus Genetics is at the forefront of developing groundbreaking gene therapies for rare inherited retinal diseases, leveraging strong financial backing and a patient-centric approach to create innovative treatments.
Keywords: gene therapy, inherited retinal diseases, biotechnology, rare eye diseases, genetic disorders, R&D, venture-backed, patient-centric, clinical trials, AAV-based therapies.