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Biomarkers, Effectiveness, and Safety of Aflibercept 8mg Modified Fixed Dose Regimen in Treatment-Naïve nAMD Patients

22 juli 2026 bijgewerkt door: Li Xiaorong, Tianjin Medical University Eye Hospital

A Prospective, Multicenter, Open-Label Phase IV Clinical Study to Evaluate the Biomarkers, Effectiveness, and Safety Based On A Modified Fixed Dose Regimen of Aflibercept 8mg in Treatment-Naïve Patients With Neovascular Age-Related Macular Degeneration (nAMD)

Primary objective:

• To evaluate the change in aqueous humor vascular endothelial growth factor A (VEGF-A) levels after 2 months of initial treatment with 8 mg Aflibercept in treatment-naïve nAMD patients.

Secondary objectives:

• To assess the efficacy, safety, and biomarker changes of 8 mg Aflibercept using a modified fixed-interval dosing regimen over 12 months in treatment-naïve nAMD patients.

Studie Overzicht

Toestand

Nog niet aan het werven

Interventie / Behandeling

Gedetailleerde beschrijving

Age-related macular degeneration (AMD) is a disease that affects the central part of the retina (the macula) and can lead to loss of central vision in older adults. In developed countries, this condition is the leading cause of central vision loss in this population. AMD has two clinical subtypes: dry and wet (neovascular) forms. The dry type is characterized by progressive accumulation of drusen, with secondary degeneration of the retinal pigment epithelium and photoreceptors; the wet type is characterized by retinal edema and neovascularization, which can lead to severe vision loss. Wet AMD is the main cause of most AMD-related blindness cases.

Inhibiting vascular endothelial growth factor (VEGF) activity with medication has been proven to be an effective therapeutic strategy for treating nAMD. In addition to Eylea® (Aflibercept) injection, multiple anti-VEGF drugs have been approved for nAMD treatment in various countries globally, such as Lucentis® (Ranibizumab), Conbercept, and Faricimab (Vabysmo®). Most nAMD patients require long-term chronic treatment. Although globally approved intravitreal (IVT) anti-VEGF therapies are effective and well tolerated, the need for frequent IVT injections (especially during the maintenance phase) places a significant burden on physicians, patients, and caregivers.

Currently, in China, local reimbursement policies for nAMD cover nine anti-VEGF injections, and patients must bear the cost for any additional treatments. As a chronic progressive disease, nAMD patients typically require longer-term management and more anti-VEGF therapies. Limitations in insurance reimbursement are a primary obstacle in clinical practice.

At the same time, anti-VEGF therapy requires a three-dose loading regimen (once per month), with frequent follow-up and a complex injection schedule, which imposes a significant financial burden on patients, increases treatment costs for physicians, results in low patient adherence, and ultimately reduces long-term visual benefits. A result from the Barometer global survey indicated that 95.2% of physicians and 83.9% of patients believe that improving the predictability of injection timing is the main direction for enhancing patient care.

Studietype

Ingrijpend

Inschrijving (Geschat)

49

Fase

  • Vroege fase 1

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

  • Naam: Xinjun Ren, PHD
  • Telefoonnummer: +86 13902067301
  • E-mail: zlrxjrsy@126.com

Studie Contact Back-up

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen
  • Oudere volwassene

Accepteert gezonde vrijwilligers

Nee

Beschrijving

Inclusion Criteria:

  1. Patients who fully understand the content, procedures, and possible adverse events (AEs) of this study and are able to provide written informed consent;
  2. Male or female patients aged ≥50 years at the time of signing the informed consent;
  3. Women of childbearing potential (WOCBP) must agree to use dual contraception during the study and for 4 months after discontinuation of study treatment, consisting of one medically recognized contraceptive method with a failure rate of less than 1% per year (see Appendix 1 for Contraceptive Measures, Definitions and Requirements for Women of Childbearing Potential) combined with a barrier method (e.g., condom). Women who have undergone surgical sterilization (such as hysterectomy, bilateral oophorectomy, or bilateral tubal ligation) or menopause for more than 1 year are considered not of childbearing potential. Women of childbearing potential must have a negative pregnancy test at screening and must not become pregnant, breastfeed, lactate, or plan pregnancy, breastfeeding, or egg donation during the study and for 4 months after discontinuation of study treatment;
  4. Male subjects whose partners are of childbearing potential must agree to use dual contraception during the study and for 4 months after the end of treatment, consisting of one medically recognized contraceptive method with a failure rate of less than 1% per year (see Appendix 1 for Contraceptive Measures, Definitions and Requirements for Women of Childbearing Potential) combined with a barrier method (e.g., condom), and must agree not to donate sperm during the study and for 4 months after the end of treatment.

    Inclusion Criteria for Study Eye

    Subjects included in this study must meet all of the following ocular inclusion criteria for the study eye:

  5. Have sufficiently clear ocular media and adequately dilated pupils to obtain high-quality retinal images for diagnosis;
  6. Untreated nAMD with active subfoveal choroidal neovascularization (CNV), with total CNV area accounting for more than 50% of the total lesion area.
  7. SD-OCT examination showed the presence of intraretinal fluid (IRF) and/or subretinal fluid (SRF) in the foveal center of the retina.
  8. During the screening and baseline periods, BCVA scores measured using the ETDRS visual acuity chart at an initial testing distance of 4 meters ranged from 78 to 24 ETDRS letters (inclusive) (approximately equivalent to Snellen visual acuity 20/32 to 20/320), and the vision loss was caused by nAMD.

Exclusion Criteria:

  1. Patients who have received other investigational treatments (including anti-VEGF, corticosteroids, laser photocoagulation treatments [panretinal photocoagulation or macular photocoagulation], and photodynamic therapy [PDT]) or approved nAMD drugs/therapies;
  2. Patients with allergies or hypersensitivity reactions to any component/excipient of the investigational product;
  3. Uncontrolled hypertension (defined as systolic blood pressure >160 mmHg or diastolic blood pressure >95 mmHg). Subjects may be treated with up to three known antihypertensive drugs to achieve adequate blood pressure control. This restriction applies to drugs that can be used for treating hypertension, even if the primary purpose of taking the drug for the subject is not blood pressure control. Any medication known to affect blood pressure must have a stable regimen for 12 weeks prior to screening;
  4. History of other diseases, metabolic dysfunctions, abnormal physical examinations, or clinical laboratory abnormalities that reasonably suggest a contraindication to the investigational drug, may interfere with the interpretation of study results, or could place the patient at high risk for treatment-related complications;
  5. Any condition that, in the opinion of the investigator, may affect the patient's ability to provide informed consent, comply with the study protocol, complete the study according to study procedures, or for which the patient's participation may affect the study results or their own safety; Exclusion criteria for study eye
  6. Any eye with diabetic retinopathy (DR), diabetic macular edema (DME), or any retinal vascular disease other than nAMD;
  7. Presence of extraocular/periocular infection or inflammation in any eye during the screening or baseline period;
  8. Presence of retinal pigment epithelium (RPE) tear or rupture, scarring, fibrosis, or atrophy involving the fovea;
  9. Fluorescein angiography (FA)/fundus photography (FP) showing:

    1. Total lesion area (including hemorrhage, scarring, and neovascularization) greater than 12 disc areas (30.5 mm²);
    2. Fibrosis or atrophy >50% of the total lesion area, and/or involving the fovea.
  10. Any intraocular disease that the investigator believes may reduce vision improvement or require medical or surgical intervention during the study (such as amblyopia, aphakia, retinal detachment, cataract, diabetic retinopathy or maculopathy, epiretinal membrane with traction):

    1. Presence of vitreous hemorrhage during the screening or baseline period;
    2. Uncontrolled glaucoma (intraocular pressure still >25 mmHg despite anti-glaucoma medication);
    3. Any cataract surgery or treatment for cataract surgery complications with steroids or yttrium-aluminum garnet (YAG) laser capsulotomy within 3 months prior to Day 1 of the study;
    4. Any prior intraocular surgery (e.g., vitrectomy, glaucoma surgery, corneal transplantation, or radiation therapy);
    5. Prior periocular or intravitreal drug injections (including anti-VEGF agents) for other retinal diseases;
    6. Presence of intraocular inflammation/infection in any eye within 12 weeks prior to the screening visit;
    7. History of idiopathic or autoimmune-related uveitis in the study eye.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: NVT
  • Interventioneel model: Opdracht voor een enkele groep
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Treatment-Naïve Patients With nAMD
Treatment-Naïve Patients With Neovascular Age-Related Macular Degeneration
All treatment-naïve nAMD patients who have completed screening and meet the eligibility criteria will be included in this study. Aflibercept 8 mg will be administered at Month 0, Month 2, Month 5, Month 8, and Month 11. A rescue treatment follow-up will be conducted at Month 1, and if the criteria for rescue treatment are met, one rescue treatment (Aflibercept 8 mg injection) will be given.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
VEGF-A levels in the patient's aqueous humor
Tijdsspanne: From enrollment to the end of treatment at 0 months、2months、5months、8months、11months
In the second month, the average change in VEGF-A levels in the patient's aqueous humor relative to baseline
From enrollment to the end of treatment at 0 months、2months、5months、8months、11months

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Proportion of patients who did not receive remedial treatment
Tijdsspanne: From enrollment to the end of treatment at 12 months
Proportion of patients who did not receive remedial treatment within 12 months
From enrollment to the end of treatment at 12 months
best corrected visual acuity (BCVA)
Tijdsspanne: From enrollment to the end of treatment at 12 months
At month 12, the changes in the patient's best corrected visual acuity (BCVA) relative to baseline
From enrollment to the end of treatment at 12 months
central retinal thickness (CMT)
Tijdsspanne: From enrollment to the end of treatment at 12 months
At month 12, the changes in the patient's central retinal thickness (CMT) relative to baseline
From enrollment to the end of treatment at 12 months
VEGF-B levels in the patient's aqueous humor
Tijdsspanne: From enrollment to the end of treatment at 0 months、2months、5months、8months、11months
In the second month, the average change in VEGF-B levels in the patient's aqueous humor relative to baseline
From enrollment to the end of treatment at 0 months、2months、5months、8months、11months
placental growth factor (PIGF) levels in the patient's aqueous humor
Tijdsspanne: From enrollment to the end of treatment at 0 months、2months、5months、8months、11months
In the second month, the average change in placental growth factor (PIGF) levels in the patient's aqueous humor relative to baseline
From enrollment to the end of treatment at 0 months、2months、5months、8months、11months
Ang-2 levels in the patient's aqueous humor
Tijdsspanne: From enrollment to the end of treatment at 0 months、2months、5months、8months、11months
In the second month, the average change in Ang-2 levels in the patient's aqueous humor relative to baseline
From enrollment to the end of treatment at 0 months、2months、5months、8months、11months
IL-6 levels in the patient's aqueous humor
Tijdsspanne: From enrollment to the end of treatment at 0 months、2months、5months、8months、11months
In the second month, the average change in IL-6 levels in the patient's aqueous humor relative to baseline
From enrollment to the end of treatment at 0 months、2months、5months、8months、11months
IL-8 levels in the patient's aqueous humor
Tijdsspanne: From enrollment to the end of treatment at 0 months、2months、5months、8months、11months
In the second month, the average change in IL-8 levels in the patient's aqueous humor relative to baseline
From enrollment to the end of treatment at 0 months、2months、5months、8months、11months
Average number of doses in the 12th month
Tijdsspanne: "From enrollment to the end of treatment at 12 months
Average number of doses in the 12th month
"From enrollment to the end of treatment at 12 months
the average area/volume of macular neovascularization (MNV)
Tijdsspanne: From enrollment to the end of treatment at 0 month、2months、5months、8months、11months
At each key visit time point, the relative change from baseline in the average area/volume of macular neovascularization (MNV) in patients ...
From enrollment to the end of treatment at 0 month、2months、5months、8months、11months
intraretinal fluid (IRF) or subretinal fluid (SRF) in the foveal area
Tijdsspanne: From enrollment to the end of treatment at 2months、12months
Percentage of patients with no intraretinal fluid (IRF) or subretinal fluid (SRF) in the foveal area at months 0, 2, and 12
From enrollment to the end of treatment at 2months、12months

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Geschat)

25 juli 2026

Primaire voltooiing (Geschat)

15 augustus 2026

Studie voltooiing (Geschat)

31 december 2027

Studieregistratiedata

Eerst ingediend

1 juli 2026

Eerst ingediend dat voldeed aan de QC-criteria

22 juli 2026

Eerst geplaatst (Werkelijk)

27 juli 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

27 juli 2026

Laatste update ingediend die voldeed aan QC-criteria

22 juli 2026

Laatst geverifieerd

1 juli 2026

Meer informatie

Termen gerelateerd aan deze studie

Aanvullende relevante MeSH-voorwaarden

Andere studie-ID-nummers

  • 2026KY-31

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

product vervaardigd in en geëxporteerd uit de V.S.

Nee

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