Stifel 2026 Healthcare Conference 2026
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Ocugen (OCGN) Stifel 2026 Healthcare Conference 2026 summary

Event summary combining transcript, slides, and related documents.

Logotype for Ocugen Inc

Stifel 2026 Healthcare Conference 2026 summary

12 Nov, 2026

Platform and pipeline

  • Modifier-gene approach uses NR2E3 for OCU400 and RORA for OCU410 and OCU410ST, targeting broad disease pathways and mutation populations.

  • OCU400 targets retinitis pigmentosa (RP); OCU410ST targets Stargardt disease in a Phase II/III trial; OCU410 targets geographic atrophy (GA) in Phase III.

  • OCU410ST topline results expected in Q2 2027, followed by BLA and market authorization applications; OCU410 is recruiting for a 240-patient global trial, with recruitment targeted for completion in 2027.

  • OCU410 received RMAT designation after Phase II data; the trial spans the U.S., Canada, and EU, with a one-year treatment period.

OCU400 clinical evidence and milestones

  • Phase I/II included three mutations; 89% of patients showed stabilization or improvement on a key functional measure, with no gene-therapy-related SAEs reported.

  • Phase III enrolls 140 patients across ~30 mutations; the primary endpoint compares the share of treated and control patients improving by two levels on a mobility test.

  • Management cited 99% statistical power for the Phase III design and said a 20% responder rate could meet the endpoint if untreated responders remain near the 0%-1% Phase I/II level.

  • Topline results expected by end-Q1 2027; planned pre-BLA meeting immediately afterward, BLA filing targeted for Q2 2027, and potential PDUFA timing in Q4 2027.

  • Europe MAA filing planned after the U.S. BLA; discussions with Japan’s PMDA are underway, with international filings to follow.

Commercial strategy

  • All programs use subretinal administration; management positions treatment as one-time and plans to expand its 30-35 trial-center network to 50-100 centers of excellence.

  • Management cited U.S. and EU pricing assumptions of $1.5 million per patient for RP and Stargardt and $450,000 for GA, describing large potential markets and one-time treatment demand.

  • Commercial planning includes payer engagement, CMS work, centers of excellence, and ex-U.S. partnerships.

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