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Enrolling by invitationPhase 2

Long-term safety follow-up of GT005 gene therapy in age-related macular degeneration

Follows people with geographic atrophy from macular degeneration treated earlier with GT005 gene therapy.

Plain-language title generated from the registry record
Registry title: ORACLE: A Long-term Follow-up Study to Evaluate the Safety of GT005 in Participants With Geographic Atrophy Secondary to Age-related Macular Degeneration Treated in a Gyroscope-sponsored Antecedent Study

Key facts

Where
London and Sunderland, United KingdomSee the 2 sites
Phase
Phase 2

Where in United Kingdom

  • The Retina Clinic LondonLondon, United KingdomNo longer taking part
  • South Tyneside and Sunderland NHS Foundation Trust - Sunderland Eye InfirmarySunderland, United KingdomNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Gyroscope Therapeutics Limited
Trial code
NCT05481827EU 2024-510946-15-00
Record updated
28 September 2026
Original description
The purpose of this study is to evaluate the long-term safety of GT005 in participants with Geographic Atrophy (GA) secondary to AMD who have been treated in an antecedent study.Read full original descriptionShow less

ORACLE: A Long-term Follow-up Study to Evaluate the Safety of GT005 in Participants With Geographic Atrophy Secondary to Age-related Macular Degeneration Treated in a Gyroscope-sponsored Antecedent Study

The purpose of this study is to evaluate the long-term safety of GT005 in participants with Geographic Atrophy (GA) secondary to AMD who have been treated in an antecedent study.

Inclusion: Able and willing to give written informed consent; Received GT005 in an antecedent study, GT005-01 (FOCUS, NCT03846193), GT005-02 (EXPLORE, NCT04437368) and GT005-03 (HORIZON, NCT04566445); Willing to attend study visits and complete the study procedures.

ClinicalTrials.gov NCT05481827 · EU CTIS 2024-510946-15-00