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A Study in Adults With Geographic Atrophy

24 maggio 2026 aggiornato da: Sitala Bio LTD

A Phase 2, Multicentre, Randomised, Double-masked, Placebo-controlled, Parallel-group, Dose-range Finding Study, to Assess the Efficacy and Safety of Oral STL303 in Adults With Geographic Atrophy Secondary to Age-related Macular Degeneration

The purpose of this clinical research study is to look at how safe STL303 is and whether it works when given to people with Geographic Atrophy (GA) secondary to Age-related Macular Degeneration (AMD). Geographic atrophy secondary to AMD is a condition where cells in the back part of the eye slowly die, causing a blurry, or missing spot in the centre of vision.

Panoramica dello studio

Stato

Non ancora reclutamento

Condizioni

Intervento / Trattamento

Descrizione dettagliata

This study is designed as a randomized, multi-center, double-masked, dose-range finding study to characterize the efficacy and safety of STL303.

Tipo di studio

Interventistico

Iscrizione (Stimato)

300

Fase

  • Fase 2

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

  • Nome: Clinical Operations Manager
  • Numero di telefono: +41815602193
  • Email: studies@sitala.com

Luoghi di studio

  • Argentina
    • Buenos Aires
      • Buenos Aires, Buenos Aires, Argentina, 1061
        • Buenos Aires Macula S.A
      • Buenos Aires, Buenos Aires, Argentina, C1120AAC
        • Centro Medico Viamonte SRL
      • Quilmes, Buenos Aires, Argentina, 1878
        • Centro de Ojos Quilmes
    • Ciudad Autonoma Buenos Aires
      • Buenos Aires, Ciudad Autonoma Buenos Aires, Argentina, 1008
        • Hospital Británico de Buenos Aires
      • Buenos Aires, Ciudad Autonoma Buenos Aires, Argentina, C1056
        • Instituoto Oftalmologico de Buenos Aires S.A.
      • Buenos Aires, Ciudad Autonoma Buenos Aires, Argentina, C1121ABB
        • Centro Oftalmologico Dr. Charles S.A.
      • Ciudad Autonoma Buenos Aires, Ciudad Autonoma Buenos Aires, Argentina, C1033AAW
        • Centro Privado de Ojos
    • Córdoba Province
      • Córdoba, Córdoba Province, Argentina, X5000
        • IMOC Instituto de Microcirugia Ocular Cordoba
    • Mendoza Province
      • Mendoza, Mendoza Province, Argentina, 5500
        • Centrovision Mendoza SA
    • Salta Province
      • Salta, Salta Province, Argentina, 4400
        • Centro de la Visión
    • Santa Fe Province
      • Rosario, Santa Fe Province, Argentina, 2000
        • Grupo Laser Visión - Rosario Eximer Laser Visión
  • Australia
    • New South Wales
      • Sydney, New South Wales, Australia, 2000
        • Sydney Eye Hospital
      • Westmead, New South Wales, Australia, 2145
        • Sydney West Retina
    • Queensland
      • South Brisbane, Queensland, Australia, 4101
        • Queensland Eye Institute
    • South Australia
      • Adelaide, South Australia, Australia, 5000
        • Adelaide Eye and Retina Centre
    • Victoria
      • East Melbourne, Victoria, Australia, 3002
        • Cerulea Pty Ltd
      • Parkville, Victoria, Australia, 3050
        • Royal Melbourne Hospital
  • Cechia
    • Prague
      • Pardubice, Prague, Cechia, 530 02
        • OFTEX, s.r.o.
      • Prague, Prague, Cechia, 100 34
        • Fakultni nemocnice Kralovske Vinohrady
      • Prague, Prague, Cechia, 150 00
        • AXON Clinical s.r.o.
  • Polonia
      • Bielsko-Biala, Polonia, 43-309
        • Szpital Swietego Lukasza S. A.
      • Bydgoszcz, Polonia, 85-631
        • Prywatna Klinika Okulistyczna OFTALMIKA
      • Bydgoszcz, Polonia, 00-189
        • Specjalistyczny Osrodek Okulistyczny Oculomedica
      • Katowice, Polonia, 40-156
        • Clinical Medical Research Sp. z o.o.
      • Katowice, Polonia, 40-594
        • Specjalistyczna Praktyka Lekarska Prof. Edward Wylęgała
      • Krakow, Polonia, 31-070
        • Centrum Medyczne Dietla 19
      • Olsztyn, Polonia, 10-424
        • Centrum Diagnostyki i Mikrochirurgii Oka LENS
      • Poznan, Polonia, 60-538
        • Poznanskie Centrum Wzroku sp z o o
      • Warsaw, Polonia, 00-189
        • Centrum Zdrowia MDM
      • Wałbrzych, Polonia, 58304
        • Centrum Medyczne
  • Regno Unito
    • Greater London
      • London, Greater London, Regno Unito, W1G 7LB
        • The Retina Clinic London
    • Hampshire
      • Southampton, Hampshire, Regno Unito, SO16 6YD
        • Southampton General Hospital
    • Leicestershire
      • Leicester, Leicestershire, Regno Unito, LE5 4PW
        • University Hospitals of Leicester NHS Trust
    • Tyne & Wear
      • Newcastle upon Tyne, Tyne & Wear, Regno Unito, NE1 4LP
        • Royal Victoria Infirmary
  • Stati Uniti
    • California
      • Bakersfield, California, Stati Uniti, 93309
        • California Retina Consultants
        • Investigatore principale:
          • Dilsher Dhoot
      • Beverly Hills, California, Stati Uniti, 90211
        • Retina-Vitreous Associates Medical Group
        • Investigatore principale:
          • Homayoun Tabandeh
      • Oakland, California, Stati Uniti, 94612
        • Kaiser Permanente - Oakland
        • Investigatore principale:
          • Robin Vora
    • Colorado
      • Aurora, Colorado, Stati Uniti, 80012
        • Retina Specialists of Colorado
        • Investigatore principale:
          • Michael Jansen
    • Connecticut
      • Waterford, Connecticut, Stati Uniti, 06385
        • Retina Group of New England, PC
        • Investigatore principale:
          • Nauman Chaudhry
    • Florida
      • St. Petersburg, Florida, Stati Uniti, 33711
        • Retina Vitreous Associates of Florida
      • Wildwood, Florida, Stati Uniti, 34785
        • Florida Retina Institute
        • Investigatore principale:
          • Luis Leon Alvarado
    • Illinois
      • Lemont, Illinois, Stati Uniti, 60439
        • University Retina and Macula Associates, P.C.
    • Indiana
      • Carmel, Indiana, Stati Uniti, 46032
        • Associated Vitreoretinal and Uveitis Consultants
        • Investigatore principale:
          • Ramana Moorthy
    • Maryland
      • Hagerstown, Maryland, Stati Uniti, 21740
        • Mid Atlantic Retina Specialists
        • Investigatore principale:
          • Adam Gerstenblith
      • Hagerstown, Maryland, Stati Uniti, 21740
        • Cumberland Valley Retina Consultants,P.C.
        • Investigatore principale:
          • Allen Hu
    • Massachusetts
      • Waltham, Massachusetts, Stati Uniti, 02451
        • Ophthalmic Consultants of Boston
        • Investigatore principale:
          • Chirag Shah
    • New York
      • Hauppauge, New York, Stati Uniti, 11788
        • Long Island and Queens Vitreoretinal Consultants of NY, P.C.
        • Investigatore principale:
          • Brett Rosenblatt
    • Pennsylvania
      • Erie, Pennsylvania, Stati Uniti, 16507
        • Erie Retina Research
        • Investigatore principale:
          • David Almeida
    • Tennessee
      • Nashville, Tennessee, Stati Uniti, 37203
        • Tennessee Retina, PC
        • Investigatore principale:
          • Carl Awh
    • Texas
      • Bellaire, Texas, Stati Uniti, 77401
        • Retina Consultants of Texas
        • Investigatore principale:
          • David Brown
      • Burleson, Texas, Stati Uniti, 76028
        • Star Vision Research
        • Investigatore principale:
          • Courtney Crawford
      • Schertz, Texas, Stati Uniti, 78154
        • Retina Consultants of Texas
        • Investigatore principale:
          • Jeremiah Brown
    • Wisconsin
      • Appleton, Wisconsin, Stati Uniti, 54914
        • Northeast Wisconsin Retina Associates
        • Investigatore principale:
          • Swati Agarwal Sinha
      • Wausau, Wisconsin, Stati Uniti, 54403
        • Eye Clinic of Wisconsin
        • Investigatore principale:
          • Deepak Sambhara
  • Svizzera
      • Bellinzona, Svizzera, 6500
        • Ente Ospedaliero Cantonale
      • Bern, Svizzera, 3007
        • Berner Augenklinik
      • Bern, Svizzera, 3011
        • Augenarzte Bern Zentrum Marktgasse
      • Binningen, Svizzera, 4102
        • Vista Augenklinik Binningen
      • Lausanne, Svizzera, 1006
        • Swiss Visio Montchoisi
      • Zurich, Svizzera, 8063
        • Stadtspital Triemli

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

The study eye must meet all inclusion criteria. If both eyes meet the inclusion criteria, the eye with the better visual acuity at the Screening visit will be designated as the study eye. If both eyes have the same visual acuity, the right eye will be selected as the study eye.

  1. Participants ≥60 years of age at the time of Screening (signing the ICF).
  2. Diagnosis of non-exudative AMD in both eyes, with confirmed presence of phenotypic hallmarks of AMD such as hard and/or soft drusen.

  3. The GA lesion in the study eye must meet the following criteria as determined by the central Reading Centre's assessment at Screening:

    1. Total GA area must be ≥2.5 and ≤10.16 mm2 (1 and 4 DA, respectively) as measured using SD-OCT.
    2. If GA is multifocal, at least one focal lesion must be ≥1.25 mm2 (0.5 DA), with the overall aggregate area of GA, as specified above in 3a.
    3. The entire GA lesion must be completely visualised on the 6 × 6 mm fovea-centred OCT scan and must be able to be imaged in its entirety and not contiguous with any areas of peripapillary atrophy.
    4. The entire EZ loss border must be completely visualised on the 6 × 6 mm fovea centred OCT scan as determined by the central Reading Centre's assessment at Screening; in cases where the EZ loss border is close to the grid boundary, a grid centred on the atrophic area may be used at the Baseline visit (as advised by the Reading Centre).
    5. All GA lesions must be at least 150 μm from foveal centre.
  4. Confirmed presence of any pattern of hyper-autofluorescence in the junctional zone of GA; absence of hyper-autofluorescence is exclusionary.
  5. BCVA by Early Treatment Diabetic Retinopathy Study (ETDRS) score of ≥55 letters (Snellen equivalent ≥20/70) in the study eye at the Screening visit and Baseline visit.
  6. Low luminance visual acuity (LLVA) by ETDRS score of ≥10 letters in the study eye at the Screening visit and Baseline visit.

  7. Meets the following criteria related to microperimetry:

    1. Able to detect fixation target.
    2. Fixation losses must be ≤20%.
    3. Participant is willing and able to undertake microperimetry assessment in the opinion of the Investigator.
  8. Able to take IMP or have an appropriate designee who can administer the IMP (i.e., a capable family member or caregiver).
  9. Able to provide written informed consent and willing to comply with all site visits, examinations, daily IMP administrations and dosing diary entries, and other conditions of the study protocol.
  10. Adequate clarity of ocular media, adequate pupillary dilation, and fixation to permit the collection of good quality images as determined by the Investigator.
  11. The fellow eye may have any of the following: AMD without GA, AMD with GA, or foveal GA (ongoing treatment with complement inhibitor therapies in the fellow eye is allowed).
  12. Vaccination against Neisseria meningitidis and Streptococcus pneumoniae infection are required at least two weeks prior to the start of the treatment with STL303.
  13. If not received previously, vaccination against Haemophilus influenzae type b infection should be given, if available and according to local regulations.
  14. Body mass index (BMI) ≥18 kg/m2 to ≤40 kg/m2.
  15. Participants of childbearing potential (POCBP) must use an appropriate birth control if not confirmed postmenopausal; male participants with partners of childbearing potential must agree to use highly effective contraception methods during the study and for 1 month after the last dose of the IMP.
  16. Participants must agree to refrain from donating gametes during the duration of the study and for 1 month after the last dose of the IMP.

Exclusion Criteria:

  1. Atrophic retinal disease of causality other than AMD including myopia-related maculopathy and macular dystrophies such as pattern dystrophy and Stargardt disease in either eye.
  2. Evidence of ongoing exudative AMD, polypoidal choroidal vasculopathy, or macular neovascularisation in either eye by history, OCT, fluorescein angiography (FA) or optical coherence tomography angiography (OCTA) as determined by the Reading Centre (prior IVT treatment for CNV is permitted in the fellow eye so long as the last injection was more than two years previously).
  3. Previous treatment with any ocular photodynamic therapy or laser coagulation to the macula in the study eye.
  4. Presence of active/current retinal vein occlusion in the study eye.
  5. Presence of vitreous haemorrhage in the study eye.
  6. History of retinal detachment in the study eye.

  7. Ocular conditions - either eye:

    1. Presence of at least moderate non-proliferative diabetic retinopathy (or worse) in either eye (a history of diabetes mellitus without retinopathy and mild non-proliferative diabetic retinopathy is not a criterion for exclusion).
    2. Presence of any other retinal pathology that, in the opinion of the Investigator, would confound the diagnosis or assessment of GA or would make follow-up not feasible.
    3. History of herpetic infection in either eye.
    4. Active uveitis and/or vitritis (grade trace or above) in either eye.
    5. History of idiopathic or autoimmune-associated uveitis in either eye.
    6. Active infectious conjunctivitis, keratitis, scleritis, or endophthalmitis in either eye.
    7. Spherical equivalent of the refractive error demonstrating >6 diopters of myopia or an axial length >26 mm in either eye.
    8. Intraocular surgery (including lens replacement surgery) within 3 months prior to randomisation in either eye.
    9. Yttrium Aluminium Garnet (YAG) laser in either eye within 1 month prior to randomisation.
  8. History of infection with Neisseria meningitidis, Streptococcus pneumoniae or Haemophilus influenzae type b despite vaccination.
  9. History or known human immunodeficiency virus (HIV), hepatitis B virus (HBV), or hepatitis C virus (HCV)-positivity (unless treated [for HBV and HCV only]) and achieved sustained viral response with negative polymerase chain reaction (PCR).
  10. Known ongoing immunodeficiency with or without treatment.
  11. Previous participation in a retinal gene therapy clinical study where the gene therapy was delivered to either eye.
  12. History of any prior IVT treatment for any indication other than AMD in either eye. Prior IVT treatment for CNV is permitted in the fellow eye so long as the last injection was more than two years previously.
  13. Any prior treatment for AMD in the study eye (for example, surgical, radiation, thermotherapeutic, or laser intervention), except oral supplements or minerals; prior treatment with Izervay or Syfovre is allowed in the study eye so long as 6 months have elapsed since the last treatment and so long as the participant did not experience any ocular inflammation or adverse events during the treatment with either Izervay or Syfovre. Ongoing treatment with Izervay or Syfovre is permitted in the fellow eye.
  14. Usage of systemic immunosuppressants or other immunomodulatory drugs within 90 days prior to the first administration or within 5 half-lives of the drug (whichever is longer), specifically including but not limited to cyclophosphamide, rituximab, infliximab, mycophenolate mofetil, cyclosporine, tacrolimus, sirolimus, systemic corticosteroids (inhaled or topical corticosteroids, or corticosteroids directly injected into the joints are allowed).
  15. Previous treatment with other systemic complement inhibitors within 30 days prior to the first dose, or within 5 half-lives of the drug, or within the potential period of residual effects from previous clinical studies, such as anti-sense oligonucleotide (ASO) or ribonucleic acid interference (RNAi), whichever is longer.
  16. Participants with any unstable or clinically significant medical condition that, in the opinion of the Investigator, could pose a risk of complications or interfere with participation during the course of the study.
  17. Participants with prolonged corrected QT interval (QTc) at Screening or at Baseline (QT interval corrected using Fridericia's formula [QTcF] >480 ms).
  18. Participants with clinically-relevant cardiac events within the last 2 years.
  19. Participants with significantly abnormal liver function at Screening or at Baseline: any parameter of ALT, AST, gamma glutamyl transferase (GGT) or alkaline phosphatase (ALP) >3 × upper limit of normal (ULN); serum bilirubin total >1.5 × ULN.
  20. Platelet count <75000 cells/mm3.
  21. Haemoglobin value <8 gm/dL.
  22. History of end stage liver or kidney disease requiring dialysis or transplant.
  23. History of hypersensitivity to any of the study treatments or excipients or to drugs of similar chemical classes or clinically relevant sensitivity to fluorescein dye as assessed by the Investigator.
  24. History of alcohol or drug abuse within the last 5 years.
  25. Ongoing treatment with cytochrome P450 2C8 (CYP2C8) inhibitors, or inducers or strong P-glycoprotein inhibitors.
  26. Ongoing participation in any other clinical study.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Quadruplicare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Comparatore placebo: Placebo
I partecipanti riceveranno placebo
Droga: Placebo
I partecipanti al braccio placebo riceveranno placebo
Sperimentale: STL303 dose level 1
Participants will receive STL303 dose level 1
Droga: STL303
STL303 arm participants will receive a specific dose of STL303
Sperimentale: STL303 dose level 2
Participants will receive STL303 dose level 2
Droga: STL303
STL303 arm participants will receive a specific dose of STL303

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Reduction of rate of total EZ area loss
Lasso di tempo: From baseline to Week 52
Rate of change in the area of photoreceptor loss
From baseline to Week 52

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Number of reported treatment-emergent adverse events (TEAE) and serious adverse events (SAEs)
Lasso di tempo: Baseline to week 108
Assess safety and tolerability of STL303
Baseline to week 108
Change in Retinal sensitivity
Lasso di tempo: From enrolment to end of treatment at week 104
Mesopic microperimetry using participant-customised peri-lesional grid.
From enrolment to end of treatment at week 104
Rate of disease progression (photoreceptor loss)
Lasso di tempo: From enrolment to end of treatment at week 104
Rate of change in the area of photoreceptor loss (defined as ellipsoid zone to retinal pigment epithelium thickness of 0 μm) in the study eye, as assessed by spectral-domain optical coherence tomography (SD-OCT)
From enrolment to end of treatment at week 104
Maximum serum concertation at steady-state (Cmax, ss) of STL303
Lasso di tempo: Weeks 0, 4, 12, 26, 52, 78, and 104 pre and 2 hours post dose.
Measure maximum plasma concentration at steady-state (Cmax, ss) at steady state.
Weeks 0, 4, 12, 26, 52, 78, and 104 pre and 2 hours post dose.
Determine pharmacodynamic profile of STL 303
Lasso di tempo: Weeks 0, 4, 12, 26, 52, 78 and 104 pre and 2 hours post dose.
Change from baseline in complement alternative pathway (AP) functional activity as measured by the Wieslab assay in serum
Weeks 0, 4, 12, 26, 52, 78 and 104 pre and 2 hours post dose.
Trough plasma concentration at steady-state of STL303
Lasso di tempo: Weeks 0, 4, 12, 26, 52, 78, and 104 pre and 2 hours post dose.
Measure trough plasma concentration at steady-state (Cmin, ss /Ctrough, ss),
Weeks 0, 4, 12, 26, 52, 78, and 104 pre and 2 hours post dose.
Area under plasma concentration-time curve for STL303
Lasso di tempo: Weeks 0, 4, 12, 26, 52, 78, and 104 pre and 2 hours post dose.
Measure the area under the plasma concentration-time curve over one dosing interval at steady state (AUCtau)
Weeks 0, 4, 12, 26, 52, 78, and 104 pre and 2 hours post dose.
Change in Vision-Related Quality of Life
Lasso di tempo: From Baseline to end of treatment at week 104
Change from baseline in the National Eye Institute 25 item Visual Functioning Questionnaire (NEI VFQ-25). Range: 0-100, where higher scores indicate better vision-related quality of life.
From Baseline to end of treatment at week 104

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Sitala Bio LTD

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 giugno 2026

Completamento primario (Stimato)

1 luglio 2028

Completamento dello studio (Stimato)

1 agosto 2029

Date di iscrizione allo studio

Primo inviato

12 maggio 2026

Primo inviato che soddisfa i criteri di controllo qualità

18 maggio 2026

Primo Inserito (Effettivo)

26 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

28 maggio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

24 maggio 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Termini relativi a questo studio

Parole chiave

Termini MeSH pertinenti aggiuntivi

Altri numeri di identificazione dello studio

  • STL303-202

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Descrizione del piano IPD

Individual participant data (IPD) will not be shared because participant consent and ethics approvals do not permit public data sharing. A clinical study report will be prepared at the end of the study and result will be shared with research sites and investigators will be able to discuss results with participants if needed.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

Sì

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

prodotto fabbricato ed esportato dagli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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