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Syncona Ltd GBP: Beacon presents Phase II/III data at AAO 2026

· Issued by Syncona Ltd GBP via RNS

Summary by 6ix AI

Syncona's portfolio company Beacon Therapeutics presented data from its pivotal Phase II/III VISTA trial of laru-zova, an investigational gene therapy for X-linked retinitis pigmentosa (XLRP), at the American Academy of Ophthalmology (AAO) Annual Meeting held October 9-12, 2026, in New Orleans. XLRP is a rare inherited retinal disease that causes progressive vision loss.

Key details

  • The presentation followed topline results from the VISTA trial, which Syncona announced on September 21, 2026.
  • Beacon reports the trial met its primary endpoint, which the FDA (the US drug regulator) had endorsed. The endpoint was low luminance visual acuity, an eye test of reading a chart through a dimming filter.
  • At month 12, 31.0% of the high dose group (p=0.0019) and 24.1% of the low dose group (p=0.0106) improved by at least 15 letters on that test, compared with no responders in the untreated control group. The p-values are measures of statistical significance.
  • Beacon reports early and sustained improvement in mean macular sensitivity, meaning the central retina's ability to detect light, compared with the untreated control group. Beacon also reports a favourable safety and tolerability profile, consistent with prior trials.
  • Syncona's holding in Beacon was valued at £183.4 million as at June 30, 2026, made up of £157.3 million of equity and £26.1 million of deferred consideration. The deferred consideration is Syncona's right to a single digit percentage of all future sales or licensing of XLRP products.

What’s still pending

  • Beacon plans to engage with global regulatory authorities and to start a rolling Biologics License Application (a filing seeking approval of a biologic medicine, submitted in parts), planned for later in 2026.
  • Laru-zova is not approved. Syncona says that, if approved, it could become the first approved treatment for XLRP.
  • Syncona intends to publish an updated valuation of the deferred consideration as part of its interim results.

6ix AI wrote this summary from the release below and checked it against the release.

Syncona Limited
12 October 2026
 

12 October 2026

Syncona Limited

(“Syncona”)

Beacon Therapeutics presents data from Phase II/III pivotal VISTA trial at AAO 2026

Syncona Ltd, a leading life science investor, today announces that its portfolio company, Beacon Therapeutics (“Beacon”), has presented data from its Phase II/III pivotal VISTA trial evaluating its investigational program, laru-zova, a gene therapy for the treatment of  patients with X-linked retinitis pigmentosa (“XLRP”) in a late-breaking oral presentation during Retina Subspecialty Day at the American Academy of Ophthalmology (“AAO”) Annual Meeting held 9-12 October 2026, in New Orleans, Louisiana.

The presentation followed Beacon’s topline results from the pivotal VISTA trial which were announced by Syncona on 21 September 2026. Beacon’s AAO data presentation will be available on Beacon’s website at 12:00 BST today.

Chris Hollowood, Chief Executive and Chief Investment Officer of Syncona Investment Management Limited, said: “The presentation of data from the pivotal VISTA trial is an important milestone and further strengthens our confidence in the potential of Beacon’s gene therapy, laru-zova. In addition to meeting its primary endpoint, the pivotal data has demonstrated positive outcomes across multiple measures of visual function and a favorable safety profile. This is an exciting moment for Beacon and for those living with XLRP. We look forward to continuing to support the company as it engages with global regulatory authorities and continues to advance this therapy towards patients.”

Key highlights from Beacon’s presentation

  • Late-breaking oral presentation outlined data from Beacon’s Phase II/III pivotal VISTA trial, which met its FDA-endorsed primary endpoint demonstrating statistically significant low luminance visual acuity (“LLVA”1)
  • 31.0% of participants in the high dose group (p=0.0019) and 24.1% of participants in the low dose group (p=0.0106) achieved an improvement of ≥15 letters in LLVA at month 12 as compared to no responders in the untreated control group, meaning laru-zova patients can now see smaller letters on an eye chart than they could before
  • Early and sustained improvement in change from baseline in mean macular sensitivity as measured by microperimetry was observed in patients treated with laru-zova compared with the untreated control group, meaning an improvement in the ability of the central part of the retina to detect light
  • Laru-zova demonstrated a favourable safety and tolerability profile, consistent with prior trials

Next steps

Beacon plans to engage with global regulatory authorities with initiation of a rolling Biologics License Application (“BLA”) submission planned for later this year. If approved, laru-zova could become the first approved treatment for patients with XLRP, which is a rare inherited retinal disease that causes progressive loss of vision and can ultimately lead to blindness.

Syncona’s holding in Beacon

Syncona’s holding in Beacon was valued at £183.4 million as at 30 June 2026. It comprises the value of equity (£157.3 million), and deferred consideration attributable to Syncona (£26.1 million). The valuation methodology for Syncona's equity interest in Beacon is the Price of Recent Investment, with the Series C financing announced in January 2026 being the most recent third-party mark. The deferred consideration represents Syncona’s right to a single digit percentage of all future sales or licensing of XLRP products and is valued using discounted cash flow methodology. Syncona intends to publish an updated valuation of the deferred consideration as part of its interim results.

Enquiries

Syncona Ltd

Annabel Clark

Tel: +44 (0) 20 3981 7940

FTI Consulting

Ben Atwell / Natalie Garland-Collins / Tim Stamper

Tel: +44 (0) 20 3727 1000

Notes

  1. LLVA is an eye test that measures how well you can read an eye chart when a dimming filter is placed in front of your eye.

About Syncona

Syncona is a leading life science investor focused on transforming patient outcomes by translating frontier science into therapeutic reality. Our investment manager, Syncona Investment Management Limited (SIML), actively manages a maturing portfolio of leading life science companies, which are diversified across development stage, modality and therapeutic area. Syncona is focused on delivering strong risk-adjusted returns to shareholders by building and scaling its portfolio companies to late-stage development, where significant value can be realised. SIML does this by working in close partnership with world-class academic founders and experienced management teams to develop treatments with the potential for transformational patient impact. For more information, please visit www.synconaltd.com.

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