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A Prospective Longitudinal Analysis of Faricimab (Vabysmo 6mg) For Choroidal Neovascularization in Presumed Ocular Histoplasmosis Syndrome (PLANE)

6 luglio 2026 aggiornato da: Cincinnati Eye Institute, Southwest Ohio

A Prospective Longitudinal Analysis of Faricimab (Vabysmo 6mg) For Choroidal Neovascularization in Presumed Ocular Histoplasmosis Syndrome [PLANE Study]

This study will evaluate the safety and effects, good or bad of faricimab (Vabysmo®), a drug that is approved by the U.S. Food and Drug Administration (FDA) for other retinal conditions, but its use is considered investigational when used specifically for choroidal neovascularization (CNV) related to presumed ocular histoplasmosis (POHS)

Panoramica dello studio

Stato

Reclutamento

Tipo di studio

Interventistico

Iscrizione (Stimato)

25

Fase

  • Fase 4

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: Kelye Conrad, Clinical Research Manager
  • Numero di telefono: 1+513-569-3688
  • Email: kconrad@cvphealth.com

Luoghi di studio

    • Ohio
      • Cincinnati, Ohio, Stati Uniti, 45242
        • Reclutamento
        • Cincinnati Eye Institute
        • Investigatore principale:
          • Miguel Busquets, MD
        • Contatto:
          • Kelye Conrad, Clinical Research Manager
          • Numero di telefono: 1+ 513-569-3462
          • Email: kconrad@cvphealth.com
      • Dayton, Ohio, Stati Uniti, 45459
        • Reclutamento
        • CVP Physicians Dayton
        • Contatto:
        • Investigatore principale:
          • Martin Wilkes, MD

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:

  • Age ≥18 years at the time of signing the Informed Consent Form
  • Ability to comply with study protocol requirements, in the investigator's judgment
  • Willingness to comply with study visits and procedures for the full duration of the 52-week study period
  • For women of childbearing potential: agreement to use highly effective contraception methods or practice complete abstinence during the study and for at least 3 months following the last dose of the investigational product, in accordance with local regulatory guidelines
  • For men with partners of childbearing potential: agreement to use effective contraception or practice complete abstinence during the study and for at least 3 months following the last dose of the investigational product
  • Presence of choroidal neovascularization (CNV) secondary to presumed ocular histoplasmosis syndrome (POHS), confirmed by funduscopic examination and supported by OCT imaging
  • Best-Corrected Visual Acuity (BCVA) between 20/40 and 20/400, inclusive, using the ETDRS letter score system at screening
  • Central macular subfield thickness (CST) >300 microns, as measured by spectral-domain OCT
  • No prior treatment with anti-VEGF agents in the study eye within 6 months prior to screening
  • No presence of other ocular diseases or conditions in the study eye that could confound visual outcomes, interfere with assessment of treatment efficacy, or pose a safety risk (see exclusion criteria)

Exclusion Criteria:

  • Known hypersensitivity to faricimab or any of its excipients Faricimab
  • Known hypersensitivity to contrast agents (e.g., fluorescein), dilating eye drops, disinfectants (e.g., iodine), anesthetics, or antimicrobial preparations used during the study
  • History of other significant systemic disease, non-diabetic metabolic dysfunction, abnormal physical examination findings, or clinical laboratory abnormalities that, in the opinion of the investigator, could pose a risk to the patient, interfere with study participation, or confound interpretation of study results
  • Active malignancy within 12 months prior to Day 1, except for appropriately treated carcinoma in situ of the cervix, non-melanoma skin cancer, or prostate cancer with a Gleason score ≤6 and stable PSA for >12 months
  • History of stroke (cerebrovascular accident) or myocardial infarction within 12 months prior to Day 1
  • Febrile illness within 1 week prior to Day 1
  • Pregnant or breastfeeding, or intending to become pregnant during the study or within 3 months after the final dose of faricimab

    o Women of childbearing potential must have a negative urine pregnancy test within 28 days prior to initiation and again at the baseline (Day 1) visit

  • Uncontrolled hypertension, defined as systolic BP >180 mmHg and/or diastolic BP >100 mmHg at rest; a repeat measurement ≥30 minutes later on the same day is permitted if the initial reading is elevated
  • Renal failure requiring renal transplant, hemodialysis, or peritoneal dialysis within 6 months prior to Day 1, or anticipated need for dialysis during the study
  • Participation in another investigational trial involving treatment with any drug or device (excluding vitamins/minerals) within 3 months or 5 half-lives (whichever is longer) prior to Day 1, or during the study
  • Clinically significant substance abuse within 12 months prior to screening, in the investigator's judgment
  • Use of systemic immunomodulatory treatments (e.g., IL-6 inhibitors) within 6 months or 5 half-lives (whichever is longer) prior to Day 1
  • Use of systemic corticosteroids within 1 month prior to Day 1
  • Systemic treatment for suspected or active systemic infection

    o Note: Ongoing prophylactic antibiotic therapy is allowed

  • Any prior or concomitant systemic anti-VEGF treatment within 6 months or 5 half-lives (whichever is longer) prior to Day 1
  • Use of systemic medications known to be toxic to the lens, retina, or optic nerve (e.g., deferoxamine, chloroquine/hydroxychloroquine, tamoxifen, phenothiazines, or ethambutol) within 6 months or 5 half-lives (whichever is longer) prior to Day 1
  • Receipt of any treatment resulting in systemic immunosuppression within 6 months or 5 half-lives (whichever is longer) prior to Day 1
  • Requirement for continuous use of medications or therapies listed as prohibited by the protocol

Ocular exclusion criteria for study eye:

Patients will be excluded if the study eye meets any of the following criteria:

  • Prior intravitreal anti-VEGF therapy within 6 months prior to Day 1 Faricimab
  • Presence of significant ocular pathology other than POHS that may affect visual outcomes or confound study assessments (e.g., retinal vein occlusion, proliferative diabetic retinopathy, central serous chorioretinopathy, or advanced age-related macular degeneration)
  • Presence of a visually significant cataract or other media opacity expected to affect visual acuity or interfere with fundus imaging or OCT evaluation
  • Active intraocular inflammation (e.g., iritis, uveitis, vitritis) in the study eye at screening
  • History of endophthalmitis in the study eye
  • Intraocular pressure >25 mmHg in the study eye at screening despite maximum tolerated medical therapy
  • History of vitrectomy or glaucoma filtration surgery in the study eye
  • Any planned ocular surgery in the study eye during the course of the study

Ocular exclusion criteria for non-study eye:

Patients will be excluded if the non-study eye meets any of the following criteria:

  • Presence of any ocular condition that could interfere with study assessments or the safety of the patient, including but not limited to:

    • Active ocular infection or inflammation
    • Uncontrolled glaucoma or intraocular pressure ≥ 25 mmHg despite treatment
    • Advanced diabetic retinopathy requiring immediate treatment
    • Significant media opacity preventing adequate fundus examination or imaging (e.g., dense cataract, vitreous hemorrhage)
    • History of vitrectomy or ocular surgery in the past 3 months
    • Any condition likely to require intraocular injections or ocular surgery during the study period
  • Any known hypersensitivity or allergy to components of faricimab or agents used in ocular procedures (e.g., fluorescein dye, dilating drops)
  • Any ocular comorbidity that, in the investigator's opinion, could confound the evaluation of the study eye or impact patient safety

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: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Comparatore attivo: Treatment
an intravitreal (inside the eye) injection of faricimab 6 mg at the first study visit (loading dose).
Subjects will receive an intravitreal (inside the eye) injection of faricimab 6 mg at the first study visit (loading dose). Subjects will return for monthly study visits for eye exams and imaging and additional faricimab injections may be given on an as-needed basis if specific vision or imaging criteria are met.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
CST Value
Lasso di tempo: 52 weeks
To assess central macular subfield thickness (CST) change from baseline to week 52.
52 weeks

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
BCVA
Lasso di tempo: 52 weeks
To assess change in BCVA (measured by ETDRS Letter Score) from baseline to week 52.
52 weeks
CNV Thickness
Lasso di tempo: 52 weeks
To assess change in CNV thickness from baseline to week 52.
52 weeks

Collaboratori e investigatori

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

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 luglio 2026

Completamento primario (Stimato)

1 maggio 2028

Completamento dello studio (Stimato)

1 maggio 2028

Date di iscrizione allo studio

Primo inviato

6 luglio 2026

Primo inviato che soddisfa i criteri di controllo qualità

6 luglio 2026

Primo Inserito (Effettivo)

10 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

10 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

6 luglio 2026

Ultimo verificato

1 luglio 2026

Maggiori informazioni

Termini relativi a questo studio

Parole chiave

Termini MeSH pertinenti aggiuntivi

Altri numeri di identificazione dello studio

  • ML46383

Piano per i dati dei singoli partecipanti (IPD)

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

NO

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

Sì

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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