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Effect of AIV007 by Periocular Administration in Subjects With Macular Edema Secondary to nAMD and DME

2. november 2026 oppdatert av: AiViva BioPharma, Inc.

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).

Studieoversikt

Detaljert beskrivelse

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.

Studietype

Intervensjonell

Registrering (Faktiske)

19

Fase

  • Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • California
      • Beverly Hills, California, Forente stater, 90211
        • Retina-Vitreous Associates
      • Santa Ana, California, Forente stater, 92705
        • Orange County Retina
    • Oregon
      • Eugene, Oregon, Forente stater, 97401
        • Verum Research
    • Texas
      • McAllen, Texas, Forente stater, 78503
        • Valley Retina Institute
      • Plano, Texas, Forente stater, 75075
        • Texas Retina Associates
      • San Antonio, Texas, Forente stater, 78240
        • Medical Center Ophthalmology

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

21 år til 90 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

General inclusion Criteria:

  1. Male or female subjects aged 21-90 years (inclusive) at screening
  2. BCVA in the study eye at screening and baseline/Day 1: ETDRS letter score ≤ 75 and ≥ 24 (20/32 to 20/330 Snellen equivalent)
  3. 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.
  4. Subject has documentation of anti-VEGF responsiveness
  5. Subject must provide written informed consent before any study-related procedures are performed
  6. Clear ocular media and adequate pupil dilation in both eyes to permit good-quality photographic imaging

nAMD subject

  1. The active choroidal neovascularization (CNV) is confirmed by fluorescein angiography (FA; evidence of leakage)
  2. Residual intraretinal or subretinal fluid based on SD-OCT
  3. CST ≥ 300 µm as assessed by SD-OCT
  4. Total lesion size < 10 disc areas (25.4 mm2)
  5. Absence of geographic atrophy within 200 µm of the fovea
  6. If subretinal hemorrhage is present, it must be < 50% of the total CNV lesion and/or not involve the fovea
  7. If fibrosis is present, it must be <50% of the total lesion area

DME subject

  1. Diagnosis of diabetes mellitus (Type 1 or Type 2)
  2. Subject has clinically significant DME with central involvement (CST≥300 μm by OCT)
  3. The decrease in vision in the study eye was determined by the investigator to be primarily the result of DME

Exclusion Criteria:

  1. 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
  2. Uncontrolled intraocular pressure (IOP), defined as an IOP > 25 mmHg
  3. Poorly controlled diabetes mellitus defined as hemoglobin A1c (HbA1c) >10% at screening visit
  4. 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
  5. 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
  6. History of vitreous hemorrhage within 3 months before screening in the study eye
  7. Uncontrolled systemic disease or any other condition or therapy that would make the participant unsuitable for the study
  8. 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)
  9. History of allergy or hypersensitivity to constituents of the study treatment formulation, topical iodine, ocular antimicrobial solutions, or clinically relevant hypersensitivity to fluorescein

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Ikke-randomisert
  • Intervensjonsmodell: Sekvensiell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: AIV007 low dose

Periocular injection, low dose

Periocular injection

Eksperimentell: AIV007 intermediate dose 1

Periocular injection, intermediate dose 1

Periocular injection

Eksperimentell: AIV007 intermediate dose 2

Periocular injection, intermediate dose 2

Periocular injection

Eksperimentell: AIV007 intermediate dose 3

Periocular injection, intermediate dose 3

Periocular injection

Eksperimentell: AIV007 intermediate dose 4

Periocular injection, intermediate dose 4

Periocular injection

Eksperimentell: AIV007 High dose

Periocular injection, high dose

Periocular injection

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Adverse Events
Tidsramme: Approximately 168 days

Incidence of adverse events and serious adverse events

Approximately 168 days

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Mean change from baseline in best-corrected visual acuity (BCVA)
Tidsramme: 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)
Tidsramme: Approximately 168 days

SD-OCT read by a central reading center

Approximately 168 days
Mean time to rescue medication
Tidsramme: Approximately 168 days

number of days to receive rescue medication

Approximately 168 days

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

2. mars 2023

Primær fullføring (Faktiske)

3. mars 2025

Studiet fullført (Faktiske)

3. mars 2025

Datoer for studieregistrering

Først innsendt

16. januar 2023

Først innsendt som oppfylte QC-kriteriene

16. januar 2023

Først lagt ut (Faktiske)

26. januar 2023

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

4. november 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

2. november 2026

Sist bekreftet

1. november 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Ja

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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