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

2026年7月22日 更新者: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.

調査の概要

状態

まだ募集していません

介入・治療

詳細な説明

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.

研究の種類

介入

入学 (推定)

49

段階

  • 初期フェーズ 1

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

  • 名前:Xinjun Ren, PHD
  • 電話番号:+86 13902067301
  • メール:zlrxjrsy@126.com

研究連絡先のバックアップ

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

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.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的: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.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
VEGF-A levels in the patient's aqueous humor
時間枠: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

二次結果の測定

結果測定
メジャーの説明
時間枠
Proportion of patients who did not receive remedial treatment
時間枠: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)
時間枠: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)
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠:"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)
時間枠: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
時間枠: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

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年7月25日

一次修了 (推定)

2026年8月15日

研究の完了 (推定)

2027年12月31日

試験登録日

最初に提出

2026年7月1日

QC基準を満たした最初の提出物

2026年7月22日

最初の投稿 (実際)

2026年7月27日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月27日

QC基準を満たした最後の更新が送信されました

2026年7月22日

最終確認日

2026年7月1日

詳しくは

本研究に関する用語

追加の関連 MeSH 用語

その他の研究ID番号

  • 2026KY-31

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