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

22. července 2026 aktualizováno: 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.

Přehled studie

Postavení

Zatím nenabíráme

Intervence / Léčba

Detailní popis

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.

Typ studie

Intervenční

Zápis (Odhadovaný)

49

Fáze

  • Raná fáze 1

Kontakty a umístění

Tato část poskytuje kontaktní údaje pro ty, kteří studii provádějí, a informace o tom, kde se tato studie provádí.

Studijní kontakt

  • Jméno: Xinjun Ren, PHD
  • Telefonní číslo: +86 13902067301
  • E-mail: zlrxjrsy@126.com

Studijní záloha kontaktů

Kritéria účasti

Výzkumníci hledají lidi, kteří odpovídají určitému popisu, kterému se říká kritéria způsobilosti. Některé příklady těchto kritérií jsou celkový zdravotní stav osoby nebo předchozí léčba.

Kritéria způsobilosti

Věk způsobilý ke studiu

  • Dospělý
  • Starší dospělý

Přijímá zdravé dobrovolníky

Ne

Popis

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.

Studijní plán

Tato část poskytuje podrobnosti o studijním plánu, včetně toho, jak je studie navržena a co studie měří.

Jak je studie koncipována?

Detaily designu

  • Primární účel: Léčba
  • Přidělení: N/A
  • Intervenční model: Přiřazení jedné skupiny
  • Maskování: Žádné (otevřený štítek)

Zbraně a zásahy

Skupina účastníků / Arm
Intervence / Léčba
Experimentální: 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.

Co je měření studie?

Primární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
VEGF-A levels in the patient's aqueous humor
Časové okno: 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

Sekundární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Proportion of patients who did not receive remedial treatment
Časové okno: 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)
Časové okno: 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)
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: "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)
Časové okno: 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
Časové okno: 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

Spolupracovníci a vyšetřovatelé

Zde najdete lidi a organizace zapojené do této studie.

Termíny studijních záznamů

Tato data sledují průběh záznamů studie a předkládání souhrnných výsledků na ClinicalTrials.gov. Záznamy ze studií a hlášené výsledky jsou před zveřejněním na veřejné webové stránce přezkoumány Národní lékařskou knihovnou (NLM), aby se ujistily, že splňují specifické standardy kontroly kvality.

Hlavní termíny studia

Začátek studia (Odhadovaný)

25. července 2026

Primární dokončení (Odhadovaný)

15. srpna 2026

Dokončení studie (Odhadovaný)

31. prosince 2027

Termíny zápisu do studia

První předloženo

1. července 2026

První předloženo, které splnilo kritéria kontroly kvality

22. července 2026

První zveřejněno (Aktuální)

27. července 2026

Aktualizace studijních záznamů

Poslední zveřejněná aktualizace (Aktuální)

27. července 2026

Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality

22. července 2026

Naposledy ověřeno

1. července 2026

Více informací

Termíny související s touto studií

Další relevantní podmínky MeSH

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Plán pro data jednotlivých účastníků (IPD)

Plánujete sdílet data jednotlivých účastníků (IPD)?

NE

Informace o lécích a zařízeních, studijní dokumenty

Studuje lékový produkt regulovaný americkým FDA

Ne

Studuje produkt zařízení regulovaný americkým úřadem FDA

Ne

produkt vyrobený a vyvážený z USA

Ne

Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .

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