Currently, there is no known cure for retinitis pigmentosa (RP). Even if some treatments can slow down the progression of the disease, none of them can effectively stop retinal degeneration. This study exploits the possibility of an early intervention in photoreceptor progenitors aiming at preventing cell death. For this purpose, we selected the rd10 mouse model, which carries a point mutation in a gene associated with human RP. We designed a CRISPR/Cas9 gene editing system to repair the mutation taking advantage of the increased activity of the homologous directed repair mechanism in dividing cells. The efficiency of the editing system (composed of guide RNA, Cas9, and DNA repair template) was first tested in vitro in neural progenitor cells derived from rd10 mice (52.8±11.1%, n=3). The constructs were then injected in vivo in the subretinal space of rd10 pups either at postnatal day (P) 3 (early treated, ET) or at P8 (late treated, LT); we also tried a P3-P8 combined treatment (multiple treated, MT). One eye was injected, while the other one was kept as internal control. The injection was followed by electroporation (electric field: 40 V/cm). Histological analysis of the eyes showed GFP expression in the photoreceptors layer starting from 2 days after electroporation. The visual acuity was measured at P30, P60 and P90 with the optomotor response test in ET, MT, LT, sham treated (ST), non-treated rd10 (NT), and WT (WT) mice. The treated eye showed a higher visual acuity than the control eye in ET, MT and LT for all the time points tested, despite a decreased visual acuity at P90 (p<0.01, one-tailed Student’s t-test). ET, MT, and LT mice had a significantly higher visual acuity compared to ST and NT mice for all the time points tested (p<0.01, one-way ANOVA + Tukey). Moreover, in order to test the integrity of the cortical visual pathway, the flash visually evoked potentials (fVEPs) were recorded from the visual cortex of ET, MT, LT, ST, NT, and WT mice at P90. We observed a partial recovery of the light-evoked response in the visual cortex of ET and LT mice (n.s and p<0.05; one-way ANOVA + Tukey), compared to ST and NT mice. Our results strongly suggest a positive effect of the CRISPR/Cas9-based therapy on photoreceptors survival in our model of RP. In the future, we would like to perform additional morphological analyses to better understand the correlation between the injection site in the retina and the specificity of the targeted visual circuits.