Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 9:18 PM
Ignite Modification Date:
2025-12-24 @ 9:18 PM
NCT ID:
NCT05282004
Eligibility Criteria:
Inclusion Criteria:
* Patients ≥ 50 years of age at baseline
* Patients diagnosed with nAMD (uni- or bilateral)
* Patients already under IVT Eylea treatment (last injection of the induction period or maintenance phase)
* Willing and able to comply with all study procedures, and be likely to complete the study
* Signed informed consent must be obtained before any assessment is performed
Exclusion Criteria:
* Active, suspected or recent (within 4 weeks) intraocular inflammation (grade trace or above) in the study eye at baseline, which is of clinical significance according to the investigator's judgment, such as active infections of the anterior segment; this includes conjunctivitis (except mild blepharitis), keratitis, scleritis, idiopathic or autoimmune associated uveitis or endophthalmitis
* Any uncontrolled ocular hypertension or glaucoma in the study eye (defined as IOP ≥ 26 mmHg, despite treatment with anti-glaucomatous medication)
* History of a medical, ocular or non-ocular condition, that in the judgment of the investigator, would preclude a safe administration of investigational product
* Visual acuity Score (VAS) worse than 20/200 on a Snellen chart, the generally accepted level of legal blindness
* Topical ocular corticosteroids administered for at least 30 consecutive days within 3 months prior to screening
* Systemic treatment with long-acting corticosteroids (more than 10 mg prednisolone equivalent) within 3 months prior to screening Current or planned use of systemic medications known to be toxic to the lens, retina or optic nerve, including deferoxamine, chloroquine/hydroxychloroquine, tamoxifen, phenothiazines and ethambutol
* Any invasive intraocular surgery, prior long-acting therapeutic agent, or ocular drug release device implantation (approved or investigational) in the study eye any time during the past 3 months
* Receipt of any systemic anti-VEGF within the last 6 months prior to enrollment
* Uncontrolled hypertension (defined as a systolic value ≥ 160 mmHg or diastolic value ≥ 100 mmHg at Screening)
* Participants who do not comply with the local COVID-19 regulations of the study site
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
50 Years
Study:
NCT05282004
Study Brief:
Protocol Section:
NCT05282004