SparingVision’s lead asset SPVN06 clears IND application in the US for the treatment of retinitis pigmentosa
SparingVision has also submitted a clinical trial authorisation (CTA) application to the French regulator (ANSM), which is currently under review.
- SparingVision has also submitted a clinical trial authorisation (CTA) application to the French regulator (ANSM), which is currently under review.
- First safety data are anticipated in 2023 and the primary endpoint is expected to be reached in 2025.
- With over 80 genes involved in RP, each with numerous causative mutations, we need to go beyond the gene-by-gene treatment approach.
- SPVN06 has the potential to become the universal therapeutic solution that patients need, and we are excited for the next phase of development.