Esta página se tradujo automáticamente y no se garantiza la precisión de la traducción. por favor refiérase a versión inglesa para un texto fuente.

Teprotumumab N01 Versus Methylprednisolone After Urgent Orbital Decompression for Dysthyroid Optic Neuropathy

17 de mayo de 2026 actualizado por: Huasheng Yang, Sun Yat-sen University

A Single-Center, Prospective, Randomized, Open-Label, Parallel-Group Study Comparing Sequential Teprotumumab N01 With Intravenous Methylprednisolone After Urgent Orbital Decompression in Patients With Dysthyroid Optic Neuropathy

This study aims to evaluate the efficacy and safety of sequential Teprotumumab N01 compared with intravenous methylprednisolone (IVMP) after urgent orbital decompression in patients with dysthyroid optic neuropathy (DON).

Descripción general del estudio

Descripción detallada

This study is designed to evaluate the efficacy and safety of sequential systemic treatment after urgent orbital decompression in patients with dysthyroid optic neuropathy.

All eligible participants will undergo standardized urgent orbital decompression. After surgery, participants will be randomized in a 1:1 ratio to receive either sequential Teprotumumab N01 or intravenous methylprednisolone. The study will compare visual function recovery, orbital signs, disease activity, quality of life, rescue treatment, recurrence, and safety between the two treatment groups.

The primary outcome is the change from baseline in best-corrected visual acuity at Week 24. Secondary outcomes include changes in visual field mean deviation, Clinical Activity Score, proptosis, diplopia, color vision, Graves' Orbitopathy Quality of Life questionnaire score, rescue treatment, recurrence, and adverse events.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

60

Fase

  • Fase 2

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

  • Nombre: Hui jing Ye, M.D, PhD
  • Número de teléfono: +8620-87331539
  • Correo electrónico: yehuijing@qq.com

Copia de seguridad de contactos de estudio

  • Nombre: Gesang Zhuoma
  • Número de teléfono: +86-18008941211
  • Correo electrónico: 1139148653@qq.com

Ubicaciones de estudio

    • Guangdong
      • Guangzhou, Guangdong, Porcelana, 510000
        • Zhongshan Ophthalmic Center, Sun Yat-sen University

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

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

Inclusion Criteria:

  • Able and willing to provide written informed consent.
  • Age 18 to 65 years.
  • Clinical diagnosis of thyroid eye disease (TED) with dysthyroid optic neuropathy (DON). Diagnosis of DON must meet both of the following criteria:

    1. Visual dysfunction not explained by other causes, such as decreased best-corrected visual acuity, visual field defect, abnormal color vision, or relative afferent pupillary defect.
    2. Imaging evidence of orbital apex crowding, optic nerve compression, or optic nerve stretching.
  • The study eye meets the criteria for urgent orbital decompression, defined as either of the following:

    1. Poor response after rescue intravenous methylprednisolone for the current dysthyroid optic neuropathy episode, with a cumulative methylprednisolone-equivalent dose of no more than 3.0 g, defined as no improvement or continued deterioration of visual function within 1 to 2 weeks.
    2. Contraindication to glucocorticoids or investigator judgment that direct urgent mechanical decompression is required.
  • Thyroid function is normal or mildly abnormal before enrollment, with free triiodothyronine (FT3) and free thyroxine (FT4) within 50% above or below the normal reference range when possible.
  • Alanine aminotransferase (ALT) no more than 1.5 times the upper limit of normal, aspartate aminotransferase (AST) no more than 3 times the upper limit of normal, and serum creatinine no more than 1.5 times the upper limit of normal.
  • For participants with diabetes mellitus, hemoglobin A1c (HbA1c) less than 9.0% and stable antidiabetic treatment within 60 days before enrollment.
  • For women of childbearing potential, a pregnancy test must be negative before enrollment.
  • Participants of reproductive potential agree to use effective contraception during the study and for 90 days after the last dose of study treatment.
  • Able and willing to comply with study treatment and follow-up procedures.

Exclusion Criteria:

  • Orbital decompression surgery within 6 months before screening.
  • Bilateral dysthyroid optic neuropathy requiring urgent bilateral orbital decompression at baseline.
  • Cumulative preoperative methylprednisolone-equivalent dose greater than 3.0 g for the current dysthyroid optic neuropathy episode.
  • Systemic glucocorticoid treatment for non-thyroid eye disease within 3 months before screening with cumulative methylprednisolone-equivalent dose of 1.0 g or greater.
  • Tocilizumab or other systemic immunosuppressive treatment within 3 months before screening, or rituximab within 6 months before screening.
  • Orbital radiotherapy within 3 months before screening.
  • Previous treatment with teprotumumab.
  • Other ocular diseases that may significantly affect visual function assessment, including glaucomatous optic neuropathy, macular disease, severe cataract, or non-thyroid eye disease optic neuropathy.
  • Irreversible optic nerve damage in the study eye with very low potential for visual recovery, as judged by the investigator.
  • History of definite inner ear disease or clinically significant hearing impairment.
  • Severe cardiovascular disease.
  • Severe hepatic or renal disease.
  • Active infection or clinically significant infectious disease, including active hepatitis, HIV infection, syphilis, or active tuberculosis.
  • Active gastrointestinal ulcer.
  • Clinically significant abnormal blood test results, including white blood cell count less than 4.0 × 10^9/L, platelet count less than 80 × 10^9/L, hemoglobin less than 110 g/L in males or less than 100 g/L in females.
  • History of malignancy judged by the investigator to be unsuitable for enrollment.
  • Pregnancy or breastfeeding.
  • Known allergy to monoclonal antibodies, methylprednisolone, or any study drug excipient.
  • Uncontrolled diabetes mellitus or any other condition that, in the investigator's judgment, makes the participant unsuitable for the study.

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 paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Postoperative Sequential Teprotumumab N01
Participants in this arm will undergo urgent orbital decompression and then receive postoperative sequential Teprotumumab N01.
Teprotumumab N01 will be administered intravenously after urgent orbital decompression. The first infusion will be 10 mg/kg, followed by 20 mg/kg every 3 weeks for 7 additional infusions.
Otros nombres:
  • Teprotumumab
  • Insulin-like growth factor-1 receptor monoclonal antibody
  • IGF-1R inhibitor
Comparador activo: Postoperative Sequential Intravenous Methylprednisolone
Participants in this arm will undergo urgent orbital decompression and then receive postoperative sequential intravenous methylprednisolone.
IVMP will be administered after urgent orbital decompression at 0.5 to 1.0 g per day for 3 consecutive days, followed by oral prednisone tapering according to the participant's clinical status and investigator judgment.
Otros nombres:
  • Metilprednisolona
  • Succinato de sodio de metilprednisolona
  • Intravenous methylprednisolone pulse therapy
  • IVMP

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in Best-Corrected Visual Acuity (BCVA) From Baseline to Week 24
Periodo de tiempo: Baseline to Week 24
BCVA will be assessed using a Snellen visual acuity chart and converted to logarithm of the minimum angle of resolution (logMAR) units for analysis. Lower logMAR values indicate better visual acuity. A negative change from baseline indicates improvement.
Baseline to Week 24

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in BCVA From Baseline to Week 12
Periodo de tiempo: Baseline to Week 12
BCVA will be assessed using a Snellen visual acuity chart and converted to logarithm of the minimum angle of resolution (logMAR) units for analysis. Lower logMAR values indicate better visual acuity. A negative change from baseline indicates improvement.
Baseline to Week 12
Change in Visual Field Mean Deviation (VF-MD) Measured by Humphrey Field Analyzer
Periodo de tiempo: Baseline to Weeks 12 and 24
VF-MD will be measured in decibels using the Humphrey Field Analyzer. Higher or less negative VF-MD values indicate better visual field function. A positive change from baseline indicates improvement.
Baseline to Weeks 12 and 24
Clinical Activity Score (CAS)
Periodo de tiempo: Baseline to Weeks 12 and 24
CAS will be used to assess disease activity in thyroid eye disease (TED). The 7-item CAS (CAS-7) will be used at baseline and ranges from 0 to 7. The 10-item CAS (CAS-10) will be used during follow-up and ranges from 0 to 10. Higher scores indicate more active inflammation, greater recent disease progression, and worse disease activity.
Baseline to Weeks 12 and 24
Proptosis Measured by Hertel Exophthalmometry
Periodo de tiempo: Baseline to Weeks 12 and 24
Proptosis will be measured in millimeters using a Hertel exophthalmometer. Higher values indicate greater proptosis. A negative change from baseline indicates improvement.
Baseline to Weeks 12 and 24
Change in Gorman Diplopia Score
Periodo de tiempo: Baseline to Weeks 12 and 24
Diplopia will be graded using the Gorman diplopia score. Scores range from 0 to 3, where 0 indicates no diplopia, 1 indicates intermittent diplopia, 2 indicates inconstant diplopia, and 3 indicates constant diplopia. Higher scores indicate worse diplopia. A negative change from baseline indicates improvement.
Baseline to Weeks 12 and 24
Color Vision Measured by Farnsworth Panel D-15 and Farnsworth-Munsell 100 Hue Tests
Periodo de tiempo: Baseline to Weeks 12 and 24
Color vision will be assessed using the Farnsworth Panel D-15 test and the Farnsworth-Munsell 100 Hue test. The Farnsworth Panel D-15 test will be recorded as normal or abnormal color discrimination. The Farnsworth-Munsell 100 Hue test will be recorded using the total error score, with lower scores indicating better color discrimination. A decrease in total error score from baseline indicates improvement.
Baseline to Weeks 12 and 24
Graves' Orbitopathy Quality of Life Questionnaire Score(GO-QOL)
Periodo de tiempo: Baseline to Weeks 12 and 24
The GO-QOL is a 16-item disease-specific questionnaire designed to measure health-related quality of life in patients with Graves' ophthalmopathy. It comprises two subscales: visual functioning (8 items) and appearance (8 items). Scores for each subscale are transformed to a range of 0 (worst possible quality of life) to 100 (best possible quality of life). A higher score indicates better quality of life. A positive change from baseline indicates improvement.
Baseline to Weeks 12 and 24
Incidence of Adverse Events and Serious Adverse Events
Periodo de tiempo: Baseline to Weeks 12 and 24
Adverse events and serious adverse events will be recorded throughout the study period. The incidence, severity, seriousness, and relationship to study treatment will be summarized by treatment group.
Baseline to Weeks 12 and 24

Colaboradores e Investigadores

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

Patrocinador

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 (Estimado)

1 de agosto de 2026

Finalización primaria (Estimado)

1 de diciembre de 2027

Finalización del estudio (Estimado)

1 de abril de 2028

Fechas de registro del estudio

Enviado por primera vez

5 de mayo de 2026

Primero enviado que cumplió con los criterios de control de calidad

17 de mayo de 2026

Publicado por primera vez (Actual)

19 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

19 de mayo de 2026

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

17 de mayo de 2026

Última verificación

1 de mayo de 2026

Más información

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. .

Suscribir