Cette page a été traduite automatiquement et l'exactitude de la traduction n'est pas garantie. Veuillez vous référer au version anglaise pour un texte source.

A Study About the Safety of a Single ASP2020 Eye Injection and if it Helps People With Vision Loss From Stargardt-type Eye Conditions

15 septembre 2026 mis à jour par: Astellas Institute for Regenerative Medicine

A Phase 1b, Open-label, Multicenter Dose-escalation Study to Evaluate the Safety, Tolerability, and Preliminary Efficacy of a Single Subretinal Dose of ASP2020 in Participants With Macular Dystrophies With a Stargardt-type Clinical Presentation

Macular dystrophies are a group of inherited eye conditions that affect the macula. The macula is in the center of the retina, the light sensitive part at the back of the eye. In people with macular dystrophies, some of the cells in the macula gradually stop working and may die over time. This leads to loss of central vision, which can make it harder to read, recognize faces or see fine details. What's seen out of the corner of the eye (peripheral vision) is mostly unaffected. Stargardt disease (STGD) is a type of macular dystrophy which is caused by 1 faulty gene (ABCA4). Vision loss most typically begins in childhood or teenage years but may also develop in adulthood. As well as STGD, there are other macular dystrophies that look very similar to STGD and are called STGD-like macular dystrophies. These are caused by many other different genes. Together, STGD and STGD-like conditions can be called STGD-type macular dystrophies.

This is an early development study of ASP2020 in adults, teenagers, and children with STGD-type macular dystrophies. ASP2020 are human stem cells which have been changed into cells found in the macula. In this study ASP2020 will be given to people for the first time. The main aim of the study is to check the safety of ASP2020 and how well people tolerate it. Other aims are to learn if people have an immune reaction to ASP2020, and if there are signs that the stem cells replace damaged cells in the retina, and vision improves for people with STGD-type macular dystrophies.

ASP2020 will be given as a single injection into the eye, under the retina. This requires a surgical procedure where the person is put to sleep by a general anesthetic. At the end of surgery, a steroid will be injected into the eye to reduce any swelling.

The study has 2 parts. In Part 1, different small groups will receive a lower to higher dose of ASP2020. This is done to find a suitable dose to use in Part 2. The adults will receive the lower dose and higher dose before the teenagers. There will be a 6-month gap between the last adult receiving the lower dose of ASP2020 and the first teenager receiving the same lower dose. This will also happen for the last adult receiving the higher dose of ASP2020 and the first teenager receiving the higher dose of ASP2020. Any medical problems will be recorded for each dose in each group. Children will not receive ASP2020 in Part 1.

In Part 2, different groups of adults, teenagers and children will receive the most suitable dose of ASP2020 worked out from Part 1.

People will be in the study for about 1 year and they will visit the clinic several times. In both parts of the study, safety checks will be done at each visit, and the study doctors will continue to check for any medical problems throughout the study. Various eye tests and eye imaging will be done throughout the study. Blood tests will also be done at some of the visits during the study.

Aperçu de l'étude

Type d'étude

Interventionnel

Inscription (Estimé)

30

Phase

  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Lieux d'étude

    • Arizona
      • Phoenix, Arizona, États-Unis, 85020
        • Recrutement
        • Associated Retina Consultants
    • Ohio
      • Cincinnati, Ohio, États-Unis, 45242
        • Recrutement
        • Cincinnati Eye Institute
    • Texas
      • Dallas, Texas, États-Unis, 75231
        • Recrutement
        • Retina Foundation of Southwest

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Enfant
  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Non

La description

Inclusion Criteria:

  • Documented clinical diagnosis of macular dystrophy with a STGD-type clinical presentation and molecular confirmation, defined as either:

    • STGD: presence of biallelic (pathogenic or likely pathogenic) ABCA4 variants, or one definite disease-causing ABCA4 variant together with a typical phenotype consistent with STGD.
    • STGD-like macular dystrophy: presence of one or more pathogenic variants in a gene known to cause macular dystrophy, as appropriate for its expected inheritance mode.
  • Sufficiently clear ocular media and adequate pupillary dilation to allow for all imaging procedures.
  • Intraocular pressure (IOP) of ≤ 21 mmHg
  • Participant has a spherical equivalent refractive error between +8.00 D and -10.00 D.
  • BCVA ranging from 20/500 to 20/40 (equivalent to 15 to 70 ETDRS letters)

    • For participants in the > 20/80 to ≤ 20/40 BCVA range (moderate visual impairment [MVI]): presence of a visible definite or probable residual ellipsoid zone (EZ) on SD-OCT, and a total retinal SD-OCT central subfield thickness ≥ 150 micrometers (µm)
    • For participants in the ≥ 20/500 to ≤ 20/80 BCVA range (severe visual impairment): Presence of a residual ONL within the macular optical coherence tomography (OCT) scan area and Evidence of RPE disease/damage by means of SD-OCT (hypertransmission defect) and/or FAF imaging (questionably decreased autofluorescence/definitely decreased autofluorescence).

Exclusion Criteria:

  • Participant has a known history of significant systemic disease that could impact ocular health or confound study assessments, based on medical history or prior clinical documentation.
  • Participant has an autoimmune condition that requires treatment with immunomodulatory therapy and/or biologics that cause immunosuppression.
  • Participant has known diagnosis of diabetes mellitus with a documented glycated hemoglobin (HbA1c) value ≥ 7% 3 months prior to screening and based on available medical records.
  • Participant has a history or evidence of severe cardiac disease, cardiovascular or cerebrovascular disease, including a history of stroke within 12 months prior to screening.
  • Participant has any complicating systemic disease or active malignancy.
  • Participant has a known history of any systemic or metabolic condition, or physical examination finding that may significantly affect ocular health or interfere with the interpretation of study assessments.
  • Participant has presence of another known or suspected molecular diagnosis of macular or retinal disease that could confound interpretation of study outcomes, indicate a second concomitant retinal condition, or suggest a different etiology for the macular disease.
  • Participant has macular atrophy due to any cause other than a genetically or clinically confirmed diagnosis of STGD or STGD-like macular dystrophy.
  • Participant has evidence or history of choroidal neovascularization.
  • Participant has diagnosis of any form of uncontrolled glaucoma (for high-tension glaucoma IOP > 25 mmHg).
  • Participant has a history of steroid-induced IOP elevation or known steroid responder status.
  • Participant has and/or is receiving treatment for thyroid eye disease.
  • Participant has diabetic retinopathy in excess of mild nonproliferative diabetic retinopathy
  • Participant has any other disease(s) affecting the optic nerve.
  • Participant has a history of anterior or posterior uveitis and/or presence of intraocular inflammation (trace anterior chamber cell or flare), or history of idiopathic or autoimmune-associated uveitis in either eye.
  • Participant has media opacities impeding the visualization of the fundus and/or the reliable performance of the visual function tests required by the protocol.
  • Participant has aphakia.
  • Participant has a clinically significant epiretinal membrane or evidence of clinically significant vitreomacular traction syndrome.
  • Participant has any other disorders which could interfere with or confound visual acuity and other ocular assessments, including OCT or FAF.
  • Participant has history of any of the following procedures: posterior vitrectomy, retinal detachment surgery, glaucoma filtering surgery, glaucoma drainage device implantation, selective laser trabeculoplasty, full-thickness or partial- thickness corneal transplant.
  • Participant has had any intraocular surgery within 3 months of screening.
  • Participant has a history of intraocular metallic foreign bodies.
  • Participant has received any treatment including gene therapy, stem cell therapy, surgical implantation of prosthetic retinal chips, or any prior intravitreal treatment for any indication in either eye that may be considered to potentially interfere with the study participation or its conduct.
  • Participant has received within 1 month prior to screening or is receiving concomitant treatment with any ocular or systemic medication known to be toxic to the lens, retina, or optic nerve.
  • Participant has received any investigational therapy within 3 months prior to screening.
  • Participant has any condition, which makes the participant unsuitable for study participation.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation séquentielle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Part 1 Dose Escalation: Adult - Low Dose
Adult participants will receive a single low dose of ASP2020 on Day 1, administered by subretinal injection as part of a surgical procedure, followed by triamcinolone acetonide as adjunct treatment by posterior sub-Tenon injection.
Subretinal Injection
Expérimental: Part 1 Dose Escalation: Adult - High Dose
Adult participants will receive a single high dose of ASP2020 on Day 1, administered by subretinal injection as part of a surgical procedure, followed by triamcinolone acetonide as adjunct treatment by posterior sub-Tenon injection.
Subretinal Injection
Expérimental: Part 1 Dose Escalation: Adolescent - Low Dose
Adolescent participants will receive single low dose of ASP2020 by subretinal injection on Day 1 followed by triamcinolone acetonide as adjunct treatment by posterior sub-Tenon injection.
Subretinal Injection
Expérimental: Part 1 Dose Escalation: Adolescent - High Dose
Adolescent participants will receive single high dose of ASP2020 by subretinal injection on Day 1 followed by triamcinolone acetonide as adjunct treatment by posterior sub-Tenon injection.
Subretinal Injection
Expérimental: Part 2 Dose Expansion: Adult with macular dystrophies
Adult participants will receive single optimal dose of ASP2020 established in part 1 by subretinal injection on Day 1 followed by triamcinolone acetonide as adjunct treatment by posterior sub-Tenon injection.
Subretinal Injection
Expérimental: Part 2 Dose Expansion: Pediatric with macular dystrophies
Pediatric participants will receive single optimal dose of ASP2020 established in part 1 by subretinal injection on Day 1 followed by triamcinolone acetonide as adjunct treatment by posterior sub-Tenon injection.
Subretinal Injection

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Number of participants with treatment-emergent adverse events (TEAEs)
Délai: Up to 52 weeks

An adverse event (AE) is defined as any untoward medical occurrence in a patient or clinical study participant, temporally associated with the use of study intervention, whether or not considered related to the study intervention.

TEAEs are defined as an AE observed after administration of ASP2020 or pre-existing AE that worsen in severity or frequency following administration of ASP2020.

Up to 52 weeks
Number of participants with serious adverse events (SAEs)
Délai: Up to 52 weeks
An SAE is defined as any untoward medical occurrence that, at any dose results in death, is life-threatening, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly/birth defect, or other medically important events.
Up to 52 weeks
Number of participants with adverse events of special interest (AESIs)
Délai: Up to 52 weeks

AESIs include, but are not limited to, the following:

  • Ectopic, excessive, or aberrant cell growth of ASP2020, including proliferative changes
  • Immune-mediated reactions, including unexpected or clinically significant inflammatory responses
  • Any new diagnosis of malignancy
  • Any clinically significant AEs possibly or definitely related to ASP2020
  • Clinically significant AEs related to the surgical administration procedure
Up to 52 weeks
Number of participants with greater than or equal to 15 letter loss in best corrected visual acuity (BCVA) from baseline
Délai: Up to 52 weeks
BCVA will be measured from the Early Treatment of Diabetic Retinopathy Study (ETDRS) letters chart.
Up to 52 weeks
Number of participants with significant changes in vital signs from baseline
Délai: Up to 52 weeks
Number of participants with significant changes in vital signs from baseline will be reported.
Up to 52 weeks
Number of participants with significant changes in laboratory values from baseline
Délai: Up to 52 weeks
Number of participants with significant changes in laboratory values from baseline will be reported.
Up to 52 weeks

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Change from baseline in BCVA
Délai: Baseline and week 26, 52 or Early Termination (ET) visit whichever occurs first
BCVA will be measured from the ETDRS letters chart.
Baseline and week 26, 52 or Early Termination (ET) visit whichever occurs first
Change from baseline in low luminance visual acuity (LLVA)
Délai: Baseline and week 26, 52 or ET visit whichever occurs first
LLVA will be measured from the ETDRS letters chart.
Baseline and week 26, 52 or ET visit whichever occurs first
Change from baseline in Minnesota Reading Acuity Chart (MNREAD) parameters
Délai: Baseline and week 26, 52 or ET visit whichever occurs first
MNREAD evaluates near reading acuity, reading speed and critical print size.
Baseline and week 26, 52 or ET visit whichever occurs first
Change from baseline in mesopic macular sensitivity
Délai: Baseline and week 26, 52 or ET visit whichever occurs first
Mean sensitivity, point-wise sensitivity (PWS), scotomatous/non-seen point count) will be measured by mesopic microperimetry.
Baseline and week 26, 52 or ET visit whichever occurs first
Change from baseline in central retinal thickness (CRT)
Délai: Baseline and week 26, 52 or ET visit whichever occurs first
CRT will be measured by spectral- domain optical coherence tomography (SD-OCT).
Baseline and week 26, 52 or ET visit whichever occurs first
Change from baseline in total photoreceptor thickness (TPT)
Délai: Baseline and week 26, 52 or ET visit whichever occurs first
TPT will be measured by SD-OCT.
Baseline and week 26, 52 or ET visit whichever occurs first
Change from baseline in ellipsoid zone (EZ) integrity
Délai: Baseline and week 26, 52 or ET visit whichever occurs first
EZ integrity will be measured by SD- OCT.
Baseline and week 26, 52 or ET visit whichever occurs first
Change from baseline in outer nuclear layer (ONL)
Délai: Baseline and week 26, 52 or ET visit whichever occurs first
ONL will be measured by SD-OCT.
Baseline and week 26, 52 or ET visit whichever occurs first
Change from baseline in retinal pigment epithelium (RPE) integrity
Délai: Baseline and week 26, 52 or ET visit whichever occurs first
RPE structural integrity will be measured by SD-OCT.
Baseline and week 26, 52 or ET visit whichever occurs first
Change from baseline in questionably decreased autofluorescence (QDAF)
Délai: Baseline and week 26, 52 or ET visit whichever occurs first
QDAF will be measured with fundus autofluorescence (FAF).
Baseline and week 26, 52 or ET visit whichever occurs first
Change from baseline in definitely decreased autofluorescence (DDAF)
Délai: Baseline and week 26, 52 or ET visit whichever occurs first
DDAF will be measured with FAF.
Baseline and week 26, 52 or ET visit whichever occurs first
Change from baseline in anti-human leukocyte antigen (HLA) antibodies
Délai: Baseline and week 4, 12 and 52 or ET visit whichever occurs first
Anti-HLA antibodies will be measured from the serum samples.
Baseline and week 4, 12 and 52 or ET visit whichever occurs first
Change from baseline in anti herpes simplex virus thymidine kinase (HSV- TK) antibodies
Délai: Baseline and week 4, 12 and 52 or ET visit whichever occurs first
Anti HSV-TK antibodies will be measured from the serum samples.
Baseline and week 4, 12 and 52 or ET visit whichever occurs first
Change from baseline in cytokines
Délai: Baseline and week 1, 4, 12 and 52 or ET visit whichever occurs first
Cytokines will be measured from the serum samples.
Baseline and week 1, 4, 12 and 52 or ET visit whichever occurs first

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Directeur d'études: Medical Lead, Astellas Institute for Regenerative Medicine

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

10 août 2026

Achèvement primaire (Estimé)

30 septembre 2029

Achèvement de l'étude (Estimé)

30 septembre 2029

Dates d'inscription aux études

Première soumission

15 juillet 2026

Première soumission répondant aux critères de contrôle qualité

24 juillet 2026

Première publication (Réel)

29 juillet 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

16 septembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

15 septembre 2026

Dernière vérification

1 septembre 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Description du régime IPD

Access to anonymized individual participant level data will not be provided for this trial. Further details on Astellas' data sharing policy can be found at https://www.clinicaltrials.astellas.com/transparency/.

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Oui

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

S'abonner