Pipeline

We’re excited about the products we have in the pipeline and the impact they will have on patients.

Product Indication Preclin Phase One Phase Two Phase Three
KIO-301 (Intravitreal) Retinitis Pigmentosa
 
 
 
 
KIO-101 (Eyedrop) Ocular Manifestations of Rheumatoid Arthritis
 
 
 
 
KIO-201 (Eyedrop) Persistent Corneal Epithelial Defects
 
 
 
 
KIO-201 (Eyedrop) Corneal Surgical Wounds
 
 
 
 
KIO-301 received Orphan Drug Designation from the FDA on March 17, 2022.
These therapeutics are still in development and are not yet approved for commercial use.
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