Effect of AIV007 by Periocular Administration in Subjects With Macular Edema Secondary to nAMD and DME
A Phase 1 Study of the Safety, Pharmacokinetics, and Exploratory Efficacy of Periocular Administration of AIV007 in Subjects With Macular Edema Secondary to Neovascular Age-Related Macular Degeneration (nAMD) or Diabetic Macular Edema (DME)
To determine safety, pharmacokinetics, and duration of effect of periocularly administered AIV007 gel suspension in subjects with neovascular age-related macular degeneration (nAMD) or diabetic macular edema (DME).
調査の概要
状態
状態
条件
条件
介入・治療
介入・治療
詳細な説明
AIV007 is a multiple kinase inhibitor of vascular endothelial growth factor receptors (VEGFR 1, -2 & -3); fibroblast growth factor receptors (FGFR-1, -2, -3 & -4); and platelet-derived growth factor receptors (PDGFR-α & β)1. Lenvatinib is the active pharmaceutical ingredient in AIV007 formulation that is FDA-approved for oral administration for patients with advanced renal cell carcinoma (RCC), differentiated thyroid cancer (DTC), unresectable hepatocellular carcinoma (HCC), and advanced endometrial carcinoma.
. AiViva BioPharma, Inc. (AiViva) has developed a novel, thermoresponsive gel suspension of AIV007 for periocular administration to form a durable depot. This monotherapy is in development for the treatment of retinal and choroidal vascular disease (i.e., neovascular age-related macular degeneration (nAMD) & diabetic macular edema (DME)). For preclinical and clinical (AIV007-E02) studies using periocular administration, AIV007 is injected outside the eyeball and the depot forms a soft mass, referred to as posterior juxtascleral depot (PJD) placement.
研究の種類
研究の種類
入学 (実際)
入学
段階
段階
- フェーズ 1
連絡先と場所
研究場所
-
-
California
-
Beverly Hills、California、アメリカ、90211
- Retina-Vitreous Associates
-
Santa Ana、California、アメリカ、92705
- Orange County Retina
-
-
Oregon
-
Eugene、Oregon、アメリカ、97401
- Verum Research
-
-
Texas
-
McAllen、Texas、アメリカ、78503
- Valley Retina Institute
-
Plano、Texas、アメリカ、75075
- Texas Retina Associates
-
San Antonio、Texas、アメリカ、78240
- Medical Center Ophthalmology
-
-
参加基準
適格基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
General inclusion Criteria:
- Male or female subjects aged 21-90 years (inclusive) at screening
- BCVA in the study eye at screening and baseline/Day 1: ETDRS letter score ≤ 75 and ≥ 24 (20/32 to 20/330 Snellen equivalent)
- Subject must have received treatment within the 24 months before screening with intravitreal (IVT) injections of an anti-VEGF agent with the last anti-VEGF injection in the study eye being at least 6 weeks (42 days) before baseline/Day 1.
- Subject has documentation of anti-VEGF responsiveness
- Subject must provide written informed consent before any study-related procedures are performed
- Clear ocular media and adequate pupil dilation in both eyes to permit good-quality photographic imaging
nAMD subject
- The active choroidal neovascularization (CNV) is confirmed by fluorescein angiography (FA; evidence of leakage)
- Residual intraretinal or subretinal fluid based on SD-OCT
- CST ≥ 300 µm as assessed by SD-OCT
- Total lesion size < 10 disc areas (25.4 mm2)
- Absence of geographic atrophy within 200 µm of the fovea
- If subretinal hemorrhage is present, it must be < 50% of the total CNV lesion and/or not involve the fovea
- If fibrosis is present, it must be <50% of the total lesion area
DME subject
- Diagnosis of diabetes mellitus (Type 1 or Type 2)
- Subject has clinically significant DME with central involvement (CST≥300 μm by OCT)
- The decrease in vision in the study eye was determined by the investigator to be primarily the result of DME
Exclusion Criteria:
- Previous treatment for nAMD or DME in the study eye other than standard-of-care anti-VEGF IVT injection, e.g., cell therapy, brachytherapy, gene therapy
- Uncontrolled intraocular pressure (IOP), defined as an IOP > 25 mmHg
- Poorly controlled diabetes mellitus defined as hemoglobin A1c (HbA1c) >10% at screening visit
- The spherical equivalent for refractive error in the study eye of worse than 8.0 diopters of myopia (before cataract or refractive surgery) per the current prescription
- Any history of active bacterial, viral, fungal, or parasitic ocular or periocular infection, or intraocular inflammation in either eye within the 30 days before the screening Visit
- History of vitreous hemorrhage within 3 months before screening in the study eye
- Uncontrolled systemic disease or any other condition or therapy that would make the participant unsuitable for the study
- Participation in any investigational study within 60 days before the screening visit, or planned use of an investigational product or device during the study; any exposure to a prior investigational drug product must be fully washed out (at least 5 half-lives)
- History of allergy or hypersensitivity to constituents of the study treatment formulation, topical iodine, ocular antimicrobial solutions, or clinically relevant hypersensitivity to fluorescein
研究計画
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:非ランダム化
- 介入モデル:順次割り当て
- マスキング:なし(オープンラベル)
アーム数
武器と介入
参加者グループ / アーム参加者グループ / アーム |
介入・治療介入・治療 |
|---|---|
|
実験的:AIV007 low dose
Periocular injection, low dose |
Periocular injection |
|
実験的:AIV007 intermediate dose 1
Periocular injection, intermediate dose 1 |
Periocular injection |
|
実験的:AIV007 intermediate dose 2
Periocular injection, intermediate dose 2 |
Periocular injection |
|
実験的:AIV007 intermediate dose 3
Periocular injection, intermediate dose 3 |
Periocular injection |
|
実験的:AIV007 intermediate dose 4
Periocular injection, intermediate dose 4 |
Periocular injection |
|
実験的:AIV007 High dose
Periocular injection, high dose |
Periocular injection |
この研究は何を測定していますか?
主要な結果の測定
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Adverse Events
時間枠:Approximately 168 days
|
Incidence of adverse events and serious adverse events |
Approximately 168 days
|
二次結果の測定
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Mean change from baseline in best-corrected visual acuity (BCVA)
時間枠:Approximately 168 days
|
Number of Early Treatment Diabetic Retinopathy Study (ETDRS) letters |
Approximately 168 days
|
|
Mean change from baseline in central subfield thickness as measured by spectral domain optical coherence tomography (SD-OCT)
時間枠:Approximately 168 days
|
SD-OCT read by a central reading center |
Approximately 168 days
|
|
Mean time to rescue medication
時間枠:Approximately 168 days
|
number of days to receive rescue medication |
Approximately 168 days
|
協力者と研究者
研究記録日
主要日程の研究
研究開始 (実際)
研究開始
一次修了 (実際)
一次修了
研究の完了 (実際)
研究の完了
試験登録日
最初に提出
最初に提出
QC基準を満たした最初の提出物
QC基準を満たした最初の提出物
最初の投稿 (実際)
最初の投稿
学習記録の更新
投稿された最後の更新 (実際)
投稿された最後の更新
QC基準を満たした最後の更新が送信されました
QC基準を満たした最後の更新が送信されました
最終確認日
最終確認日
詳しくは
本研究に関する用語
その他の研究ID番号
その他の研究ID番号
- AIV007-E02
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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