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Safety and Efficacy Study of Novel Gene Therapy AGX-08 for Geographic Atrophy

30. juli 2026 oppdatert av: 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.

Studieoversikt

Status

Har ikke rekruttert ennå

Detaljert beskrivelse

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.

Studietype

Intervensjonell

Registrering (Antatt)

24

Fase

  • Tidlig fase 1

Kontakter og plasseringer

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

Studiekontakt

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

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Beskrivelse

Inclusion Criteria:

  1. Clinically confirmed diagnosis of geographic atrophy (GA) secondary to age-related macular degeneration (AMD);
  2. Age ≥ 50 years, regardless of sex;
  3. 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;
  4. 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;
  5. Presence of choroidal neovascularization (CNV) in the fellow eye is allowed;
  6. Women of childbearing potential must have a negative pregnancy test (blood or urine);
  7. 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;
  8. Willing and able to provide written informed consent and comply fully with the study protocol.

Exclusion Criteria:

  1. GA caused by conditions other than AMD (e.g., Stargardt disease, cone-rod dystrophy, or other inherited macular dystrophies);
  2. Aphakia in the study eye, or cataract surgery/YAG capsulotomy within 3 months prior to screening;
  3. 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;
  4. Two baseline BCVA measurements (ETDRS) taken at least 14 days apart during screening differ by >30%;
  5. 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;
  6. Active ocular diseases in the study eye, including inflammation, other macular diseases, glaucoma, ocular hypertension, or acute/chronic ocular infections;
  7. Major ocular surgery within 3 months prior to screening;
  8. History of retinal detachment or other fundus diseases unsuitable for study participation;
  9. Prior macular laser photocoagulation with irreversible retinal damage;
  10. Pregnant or lactating women, or participants unwilling to use effective contraception for 12 months before and after study intervention;
  11. Narrow anterior chamber angle or other contraindications to pupil dilation;
  12. Any ocular condition that may interfere with visual acuity assessment, OCT, or other ophthalmic evaluations;
  13. History of hypersensitivity to contrast agents, study drugs, or excipients;
  14. Allergy to corticosteroids, intolerance to protocol-required corticosteroid therapy, or contraindicated active infections;
  15. Severe systemic diseases, psychiatric disorders, uncontrolled chronic conditions, or other medical conditions that may increase study risk (e.g., malignancy, metabolic or autoimmune diseases);
  16. 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.;
  17. Receiving or likely to receive immunosuppressive therapy outside this study;
  18. Participation in another investigational drug study within 3 months prior to screening;
  19. Prior gene therapy other than this study;
  20. Any condition that may compromise scientific evaluation of the study;
  21. Any contraindication to intravitreal (IVT) injection;
  22. Any other condition deemed unsuitable by the investigator.

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: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Dobbelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Low Dose
IVT administration of a single low dose AGX-08 injection
rAAV2.AG-eNCRV intravitreal injection of low dose
Andre navn:
  • Lav dose
Eksperimentell: High Dose
IVT administration of a single high dose AGX-08 injection
rAAV2.AG-eNCRV intravitreal injection of high dose
Andre navn:
  • Høy dose
Sham-komparator: Control
Sham IVT injection
sham intravitreal injection of AGX-08 (not actual injection)
Andre navn:
  • Skum kontroll

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Incidence of treatment-emergent adverse events,adverse events, serious adverse events and dose-limiting toxicities
Tidsramme: 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

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change in Fundus Autofluorescence (FAF)
Tidsramme: 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)
Tidsramme: 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

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 (Antatt)

1. juli 2026

Primær fullføring (Antatt)

30. desember 2028

Studiet fullført (Antatt)

30. desember 2029

Datoer for studieregistrering

Først innsendt

17. mai 2026

Først innsendt som oppfylte QC-kriteriene

20. mai 2026

Først lagt ut (Faktiske)

22. mai 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

31. juli 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

30. juli 2026

Sist bekreftet

1. juli 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

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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