Grants of up to £300,000 are available for researchers seeking to conduct high-quality research projects to further understanding of the causes and potential treatments for all forms of inherited retinal disease.

Retina UK has launched a new call for its Project Grant scheme, which supports cutting edge research to investigate causes and potential treatments for all forms of inherited retinal dystrophies, including Retinitis Pigmentosa (RP) and associated syndromes.

The Project Grants are typically in the range of £250,000 and £300,000 over a maximum of three years for projects with a clear focus on developing treatments for inherited retinal disease, particularly those with clear translational potential.

Areas of enquiry can include basic laboratory research to investigate disease mechanisms, preclinical studies in animal and cell models and genotyping and phenotypic investigation of patient populations as a prelude to clinical trials. Priority is given to research that shows promise for progressing the development of treatment strategies or slowing down the progress of sight loss.

Lead applicants should have a good track record of obtaining funding from other sources and be recognised amongst their peers for their research.

Funding is generally for research based in the UK. While there is no restriction on the geographic location of applicants, consideration will only be given to projects based outside the UK if they are deemed exceptional and demonstrate meaningful collaboration with UK-based researchers

When formulating proposals, researchers should consider the research questions identified by the Sight Loss and Vision Priority Setting Partnership Priorities for Inherited Retinal Diseases that are of particular interest to Retina UK, namely:

• Can a treatment to slow down progression or reverse sight loss in inherited retinal diseases be developed?
• How can sight loss be prevented in an individual with inherited retinal disease?
• Is a genetic (molecular) diagnosis possible for all inherited retinal diseases?
• What factors affect the progression of sight loss in inherited retinal diseases?
• What causes sight loss in inherited retinal diseases?
• What is the most effective way to support patients with inherited retinal disease?
• Can the diagnosis of inherited retinal diseases be refined so that individuals can be given a clearer idea about their specific condition and how it is likely to progress?
• What is the relationship between sight loss and mental health for people with inherited retinal diseases?
• With regard to inherited retinal diseases, what is the role of pre-natal and preimplantation diagnosis in helping parents make informed choices?

A preliminary application must be submitted by the deadline on 1 April 2026.