Safety and Efficacy Study of Novel Gene Therapy AGX-08 for Geographic Atrophy
2026年7月30日 更新者:Zhongmou Therapeutics
Prospective, Dose-Escalating, Investigator Initiated Trial to Evaluate the Safety and Efficacy of AGX-08 in Geographic Atrophy
This is AGX-08's safety, tolerability, and efficacy in Geographic Atrophy first-in-human study.
This trial is meant to evaluate the safety and efficacy of AGX-08 in Geographic Atrophy patients.
Unilateral intravitreal injections (IVT) will be given into the subject's Study Eye.
調査の概要
詳細な説明
Geographic atrophy (GA) secondary to age-related macular degeneration (AMD) is a leading cause of irreversible vision loss in the elderly population.
Patients with GA experience progressive degeneration of retinal cells, resulting in gradual and permanent visual decline.
Currently, there are limited effective treatment options available.
We have developed an innovative adeno-associated virus (AAV)-based gene therapy for patients with GA, regardless of underlying genetic background.
Approximately 8 to 24 subjects with GA will be recruited, among whom a subset will receive a single unilateral intravitreal injection of AGX-08 at ascending doses, while a proportion of subjects will receive sham injections as the control group.
研究の種類
介入
入学 (推定)
24
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:Windy Zhou
- 電話番号:+86 18986214263
- メール:zmt@zmtherapeutics.com
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:
- Clinically confirmed diagnosis of geographic atrophy (GA) secondary to age-related macular degeneration (AMD);
- Age ≥ 50 years, regardless of sex;
- Best-corrected visual acuity (BCVA) in the study eye measured using the ETDRS chart at a starting distance of 4 meters must be ≤35 letters (Snellen equivalent ≤20/200), with vision no worse than light perception; the fellow eye must not have better visual acuity than the study eye;
- GA lesion size between 2.5 and 17.5 mm² with clearly defined borders. For multifocal GA, at least one lesion must be ≥1.25 mm² (0.5 disc area) to ensure measurable efficacy assessment;
- Presence of choroidal neovascularization (CNV) in the fellow eye is allowed;
- Women of childbearing potential must have a negative pregnancy test (blood or urine);
- Women of childbearing potential and male participants must agree to use effective contraception during the study and for 3 months after completion, with no plans for reproduction;
- Willing and able to provide written informed consent and comply fully with the study protocol.
Exclusion Criteria:
- GA caused by conditions other than AMD (e.g., Stargardt disease, cone-rod dystrophy, or other inherited macular dystrophies);
- Aphakia in the study eye, or cataract surgery/YAG capsulotomy within 3 months prior to screening;
- Refractive status or axial length outside the following range: spherical equivalent between -6.00D and +5.00D, and axial length between 21 mm and 26 mm;
- Two baseline BCVA measurements (ETDRS) taken at least 14 days apart during screening differ by >30%;
- Current or prior evidence of exudative (wet) AMD in the study eye, including retinal pigment epithelium tear, retinal vascular occlusions, history of corneal transplantation, or any neovascularization confirmed by fluorescein angiography;
- Active ocular diseases in the study eye, including inflammation, other macular diseases, glaucoma, ocular hypertension, or acute/chronic ocular infections;
- Major ocular surgery within 3 months prior to screening;
- History of retinal detachment or other fundus diseases unsuitable for study participation;
- Prior macular laser photocoagulation with irreversible retinal damage;
- Pregnant or lactating women, or participants unwilling to use effective contraception for 12 months before and after study intervention;
- Narrow anterior chamber angle or other contraindications to pupil dilation;
- Any ocular condition that may interfere with visual acuity assessment, OCT, or other ophthalmic evaluations;
- History of hypersensitivity to contrast agents, study drugs, or excipients;
- Allergy to corticosteroids, intolerance to protocol-required corticosteroid therapy, or contraindicated active infections;
- Severe systemic diseases, psychiatric disorders, uncontrolled chronic conditions, or other medical conditions that may increase study risk (e.g., malignancy, metabolic or autoimmune diseases);
- articipants with a prior history of malignancy must have completed curative treatment ≥5 years before enrollment and must have no evidence of active disease, recurrence, or metastasis. Participants whose prior malignancy is considered unlikely to affect life expectancy may be eligible based on Investigator assessment in consultation with an oncology specialist. The 5-year disease-free interval requirement may be waived for adequately treated cervical carcinoma in situ or non-melanoma skin cancer with minimal risk of recurrence.;
- Receiving or likely to receive immunosuppressive therapy outside this study;
- Participation in another investigational drug study within 3 months prior to screening;
- Prior gene therapy other than this study;
- Any condition that may compromise scientific evaluation of the study;
- Any contraindication to intravitreal (IVT) injection;
- Any other condition deemed unsuitable by the investigator.
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:ランダム化
- 介入モデル:並列代入
- マスキング:ダブル
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:Low Dose
IVT administration of a single low dose AGX-08 injection
|
rAAV2.AG-eNCRV intravitreal injection of low dose
他の名前:
|
|
実験的:High Dose
IVT administration of a single high dose AGX-08 injection
|
rAAV2.AG-eNCRV intravitreal injection of high dose
他の名前:
|
|
偽コンパレータ:Control
Sham IVT injection
|
sham intravitreal injection of AGX-08 (not actual injection)
他の名前:
|
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 |
|---|---|---|
|
Incidence of treatment-emergent adverse events,adverse events, serious adverse events and dose-limiting toxicities
時間枠:baseline to Week 52
|
Incidence of severity of ocular and systemic treatment-emergent adverse events, (TEAEs), adverse events (AEs) , serious adverse events (SAEs) and dose-limiting toxicities(DLTs) following a single intravitreal injection of AGX-08.
|
baseline to Week 52
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Change in Fundus Autofluorescence (FAF)
時間枠:baseline to Week 52
|
FAF is a non-invasive imaging technique that provides critical information about the health of the retina, which is vital for the functioning of the retina.
|
baseline to Week 52
|
|
Change in best corrected visual acuity (BCVA)
時間枠:baseline to Week 52
|
BCVA of both eyes will be assessed using the early treatment of diabetic retinopathy study (ETDRS) chart or tumbling "E" chart or other avaliable measurement.
This approach was chosen to facilitate visual acuity testing in subject who cannot recognize letters.
|
baseline to Week 52
|
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。
スポンサー
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1日
一次修了 (推定)
2028年12月30日
研究の完了 (推定)
2029年12月30日
試験登録日
最初に提出
2026年5月17日
QC基準を満たした最初の提出物
2026年5月20日
最初の投稿 (実際)
2026年5月22日
学習記録の更新
投稿された最後の更新 (実際)
2026年7月31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30日
最終確認日
2026年7月1日
詳しくは
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