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2024-516970-31-00CompletedPhase 2

Molecular imaging exploration of ocular angiogenic activity and evaluation of its value in therapeutic follow-up of AMD patients

Molecular imaging exploration of ocular angiogenic activity and evaluation of its value in therapeutic follow-up of AMD patients

Source: EU CTIS (euclinicaltrials.eu) · Last updated 17 Oct 2024

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Brief summary (registry, in English)

Evaluate the ability of 68Ga-NODAGA-RGD PET imaging to demonstrate, in 20 patients with unilateral AMD, a molecular therapeutic response to intraocular antiangiogenic injections at the end of the induction phase (after 3 months of treatment).

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
20 (actual)
First submitted
27 Sept 2024
Start date
2 Oct 2022
Lead sponsor
Centre Hospitalier Regional De Marseille
EU CT number
2024-516970-31-00
EudraCT number
2019-000946-37

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 20
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients previously treated with antiangiogenic therapy.

Age

  • Age ≤ 18 years

Other

  • pregnant or breast-feeding women
  • Patients with bilateral AMD
  • Patients with AMD with no neovascularization focus as assessed by the standard diagnostic battery
  • Patients suffering from any other ophthalmological pathology
  • Monophtalmic patients

Who the study is looking for

  • Age ≥ 18 years
  • signed informed consent
  • Patient with unilateral AMD, with at least 1 focus of choroidal neovascularization on OCT, naïve to any antiangiogenic treatment.
  • Initial check-up including at least OCT and visual acuity measurement, maximum 1 month old at the time of the 68Ga-NODAGA-RGD PET scan
  • affiliation to a social security scheme.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Centre Hospitalier Regional De MarseilleMarseilleFranceCompleted

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