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NCT03999801Enrolling by invitationPhase 2

Long-term Follow-Up Study of RGX-314 and Fellow Eye Substudy

A Long-term Follow-Up Study to Evaluate the Safety and Efficacy of RGX-314 Following Subretinal Administration in Participants With Neovascular Age-related Macular Degeneration and Fellow Eye Treatment Substudy

Source: ClinicalTrials.gov · Last updated 17 Jun 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This is a prospective, observational study designed to evaluate the long-term safety and efficacy of RGX-314. Eligible participants are those who were previously enrolled in a clinical study in which they received a single subretinal administration of RGX-314 in their study eye. Enrollment of each participant in the current study should occur after the participant has completed either the end of study or early termination visit in the previous (parent) clinical study. Participants will be followed for up to 5 years post-RGX-314 administration (inclusive of the parent study). After enrollment and a 6-month follow-up visit, participants will attend at least annual study visits through the end of the 5-year post-RGX-314 administration follow-up period. Additionally, an interventional fellow eye treatment substudy will evaluate the safety, efficacy, and immunogenicity of subretinal RGX-314 administration in the fellow eye of participants having bilateral disease who previously received a subretinal injection of RGX-314 in their study eye. Participants who qualify for the substudy will receive subretinal administration of RGX-314 in their fellow eye and complete 13 study visits in a 54-week period. Following completion of the substudy participants will continue in the observational portion of the study for up to 5 years post RGX-314 administration in their fellow eye.

Status (registry)
Enrolling by invitation
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
865 (estimated)
First submitted
18 Jun 2019
Start date
31 May 2019
Primary completion date
31 Dec 2028
Lead sponsor
AbbVie
NCT number
NCT03999801
EU CT number
2023-505750-17-00

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 865
  • From 31 May 2019 to the primary completion date, 31 Dec 2028
  • 47 sites in 6 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • History of intravitreal therapy, such as intravitreal steroid injection or investigational product, other than an intravitreal therapy for nAMD, in the fellow eye within 6 months of screening

Other illness

  • Advanced glaucoma or history of secondary glaucoma in the fellow eye or any invasive procedure to treat glaucoma
  • Myocardial infarction, cerebrovascular accident, or transient ischemic attack within the past 6 months
  • History of intraocular surgery in the fellow eye within 12 weeks of screening

Other

  • CNV or macular edema in the fellow eye secondary to causes other than nAMD
  • Subfoveal fibrosis or atrophy in the fellow eye

Who the study is looking for

  • Able and willing to provide written consent
  • Previously enrolled in a clinical study of RGX-314 and received a single subretinal administration of RGX-314
    • Exclusions Criteria:
    • 1\. None
    • Fellow Eye Substudy:
  • Age ≤ 93 years
  • Currently or previously enrolled in the main observational study
  • Diagnosis of bilateral choroidal neovascularization secondary to age-related macular degeneration
  • Active nAMD in the fellow eye
  • BCVA between ≤ 80 and ≥ 20 letters in the fellow eye

Criteria the registry did not label

  • Main Observational Study:

Age in the registry: 50 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (47)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Universitaetsklinikum Bonn AöR
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BonnGermanyNot yet recruiting
Medical Center- University of Freiburg
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Freiburg im BreisgauGermanyNot yet recruiting
University Medical Center Hamburg-Eppendorf
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HamburgGermanyNot yet recruiting
Klinikum der Stadt Ludwigshafen am Rhein gGmbH
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Ludwigshafen Am RheinGermanyNot yet recruiting
Universitaet Muenster
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MuensterGermanyNot yet recruiting
Universitaetsklinikum Ulm AoR
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UlmGermanyNot yet recruiting
Hospital Clinic de Barcelona
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BarcelonaSpainNot yet recruiting
Hospital de la Santa Creu i Sant Pau
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BarcelonaSpainNot yet recruiting
Instituto De Microcirugia Ocular Dos S.L.
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BarcelonaSpainNot yet recruiting
Metavision Arruzafa S.L.
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CordobaSpainNot yet recruiting
Complejo Hospitalario Universitario Insular Materno Infantil
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Las Palmas de Gran CanariaSpainNot yet recruiting
Bellvitge University Hospital
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L'hospitalet De LlobregatSpainNot yet recruiting
Clinica Baviera S.A.
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MadridSpainNot yet recruiting
Hospital Universitario 12 de Octubre
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MadridSpainNot yet recruiting
Hospital Universitario Puerta de Hierro de Majadahonda
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MajadahondaSpainNot yet recruiting
Hospital Provincial de Conxo
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Santiago de CompostelaSpainNot yet recruiting
Centre Hospitalier Intercommunal Créteil
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CréteilFranceNot yet recruiting
Centre Hospitalier Universitaire de Dijon
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DijonFranceNot yet recruiting
Hospices Civils De Lyon
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Lyon Cedex 04FranceNot yet recruiting
Centre Monticelli Paradis d'Ophtalmologie
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MarseilleFranceNot yet recruiting
Clinique Honoré Cave
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MontaubanFranceNot yet recruiting
Centre Hospitalier Universitaire de Nantes
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NantesFranceNot yet recruiting
Centre Hospitalier Universitaire de Nice
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NiceFranceNot yet recruiting
Assistance Publique Hopitaux de Paris
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ParisFranceNot yet recruiting
Centre Hospitalier Universitaire de Toulouse
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ToulouseFranceNot yet recruiting
Budapest Retina Associates Kft.
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Budapest XIIIHungaryNot yet recruiting
University of Debrecen
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DebrecenHungaryNot yet recruiting
Nozologen Kft.
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PécsHungaryNot yet recruiting
Azienda Universitaria Ospedaliera Consorziale Policlinico Bari
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BariItalyNot yet recruiting
Azienda Sanitaria Locale 2 Lanciano Vasto Chieti
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ChietiItalyNot yet recruiting
University Hospital Of Ferrara
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FerraraItalyNot yet recruiting
ASST Fatebenefratelli Sacco
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MilanItalyNot yet recruiting
Ospedale San Raffaele S.r.l.
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MilanItalyNot yet recruiting
Azienda Ospedaliera Universitaria - Universita degli Studi della Campania Luigi Vanvitelli
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NaplesItalyNot yet recruiting
IRCCS Ospedale Sacro Cuore Don Calabria
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NegrarItalyNot yet recruiting
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
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RomeItalyNot yet recruiting
Fondazione G.B.Bietti Per Lo Studio E La Ricerca In Oftalmologia
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RomeItalyNot yet recruiting
Azienda Sanitaria Universitaria Friuli Centrale
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UdineItalyNot yet recruiting
Johns Hopkins University
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BaltimoreUnited StatesUnknown status
Ophthalmic Consultants of Boston
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BostonUnited StatesUnknown status
Charles Retina Institute
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GermantownUnited StatesUnknown status
University of Pennsylvania Department of Ophthalmology
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PhiladelphiaUnited StatesUnknown status
MidAtlantic Retina
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PhiladelphiaUnited StatesUnknown status
Retinal Research Institute, LCC
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PhoenixUnited StatesUnknown status
Sierra Eye Associates
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RenoUnited StatesUnknown status
California Retina Consultants CRC
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Santa BarbaraUnited StatesUnknown status
Retina Consultants of Texas Research Center
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The WoodlandsUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.