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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 de septiembre de 2026 actualizado por: 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.

Descripción general del estudio

Estado

Reclutamiento

Condiciones

Intervención / Tratamiento

Tipo de estudio

Intervencionista

Inscripción (Estimado)

30

Fase

  • Fase 1

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Ubicaciones de estudio

    • Arizona
      • Phoenix, Arizona, Estados Unidos, 85020
        • Reclutamiento
        • Associated Retina Consultants
    • Ohio
      • Cincinnati, Ohio, Estados Unidos, 45242
        • Reclutamiento
        • Cincinnati Eye Institute
    • Texas
      • Dallas, Texas, Estados Unidos, 75231
        • Reclutamiento
        • Retina Foundation of Southwest

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Niño
  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

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 de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación Secuencial
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: 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
Experimental: 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
Experimental: 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
Experimental: 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
Experimental: 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
Experimental: 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

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Number of participants with treatment-emergent adverse events (TEAEs)
Periodo de tiempo: 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)
Periodo de tiempo: 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)
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: Up to 52 weeks
Number of participants with significant changes in laboratory values from baseline will be reported.
Up to 52 weeks

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change from baseline in BCVA
Periodo de tiempo: 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)
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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)
Periodo de tiempo: 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)
Periodo de tiempo: 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
Periodo de tiempo: 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)
Periodo de tiempo: 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
Periodo de tiempo: 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)
Periodo de tiempo: 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)
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Investigadores

  • Director de estudio: Medical Lead, Astellas Institute for Regenerative Medicine

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

10 de agosto de 2026

Finalización primaria (Estimado)

30 de septiembre de 2029

Finalización del estudio (Estimado)

30 de septiembre de 2029

Fechas de registro del estudio

Enviado por primera vez

15 de julio de 2026

Primero enviado que cumplió con los criterios de control de calidad

24 de julio de 2026

Publicado por primera vez (Actual)

29 de julio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

16 de septiembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

15 de septiembre de 2026

Última verificación

1 de septiembre de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • 2020-CL-0101

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan 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/.

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

Sí

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .