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Ocugen Reports the US FDA’s Approval of Expanded Access Program for Retinitis Pigmentosa Patients

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Ocugen

Ocugen Reports the US FDA’s Approval of Expanded Access Program for Retinitis Pigmentosa Patients

Shots:

  • The US FDA has approved the EAP program to treat early, intermediate to advanced retinitis pigmentosa (RP) in adults (≥18yrs.) having at least minimal retinal preservation with OCU400 gene therapy 
  • The company is conducting P-III (liMeliGhT) study of OCU400 (2.5 x 10^10 vector genomes/eye) for 1yr. in 150 subjects, with arm 1 incl. 75 with RHO gene mutations & arm 2 incl. 75 with other gene mutations. Subjects aged ≥8yrs. with early to late-stage RP are being recruited. The BLA & MAA approval is expected in 2026
  • OCU400 is based on the NR2E3 gene which controls photoreceptor development, metabolism, phototransduction, inflammation & cell survival in the retina
Click here to­ read the full press release 

Disha Nankani

Disha is a content writer at PharmaShots. She is passionate and curious about recent updates and developments in MedTech and Pharma industry. She covers news related to clinical trial results and updates. She can be contacted at connect@pharmashots.com.

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