![cropped-SPVN_Favicon.png cropped-SPVN_Favicon.png](https://sparingvision.com/wp-content/uploads/2021/09/cropped-SPVN_Favicon-100x100.png)
Our Company
Moving beyond single gene correction therapies to deliver new treatments.
We are a clinical-stage genomic medicines company leading a step shift in how ocular diseases are treated. We are going beyond single gene correction therapies to deliver new treatments to patients affected by Inherited Retinal Diseases (IRDs), regardless of genetic cause.
![SPVN_ICON_DNA SPVN_ICON_DNA](https://sparingvision.com/wp-content/uploads/2021/09/SPVN_ICON_DNA-100x100.png)
Genomic Medicines
Our goal is to harness the potential of gene therapy and genome editing to bring cutting-edge innovation into ocular disease drug discovery and development.
![SPVN_ICON_MIC SPVN_ICON_MIC](https://sparingvision.com/wp-content/uploads/2021/09/SPVN_ICON_MIC-100x100.png)
Pipeline
At the heart of this is a pipeline of mutation independent treatments for Inherited Retinal Diseases (IRD) such as Retinitis Pigmentosa (RP), the leading inherited cause of blindness which affects 2 million people worldwide.
![SPVN_ICON_EYE_X SPVN_ICON_EYE_X](https://sparingvision.com/wp-content/uploads/2021/09/SPVN_ICON_EYE_X-100x100.png)
Retinitis Pigmentosa
A group of IRDs which are a leading cause of blindness globally. Current monogenic treatment approaches are not applicable to all patients. With our approach we believe that we can bring meaningful differences to many of them.
![SPVN_ICON_Globe SPVN_ICON_Globe](https://sparingvision.com/wp-content/uploads/2021/09/SPVN_ICON_Globe-150x150.png)
SPVN06
SparingVision’s lead product, SPVN06, is a breakthrough gene therapy approach targeting Inherited Retinal Diseases (IRDs).
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