- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07647510
A Phase 3 Study to Evaluate Claseprubart in Adults With Generalized Myasthenia Gravis (EMERGE)
28 de agosto de 2026 actualizado por: Dianthus Therapeutics
A Phase 3 Global, Multicenter, Randomized, Double-blind, Placebo-controlled Study to Demonstrate the Efficacy, Safety, and Tolerability of Claseprubart (DNTH103) in Patients With Generalized Myasthenia Gravis (EMERGE)
The purpose of this Phase 3 study is to demonstrate the efficacy, safety, and tolerability of claseprubart in participants with generalized myasthenia gravis (gMG).
Descripción general del estudio
Estado
Reclutamiento
Condiciones
Intervención / Tratamiento
Descripción detallada
The study includes the following periods:
- Screening (up to 12 weeks)
- Randomized, blinded, controlled treatment (RCT) period (17 weeks)
- Extended treatment period (ETP) (104 weeks) (optional) for eligible participants [includes blinded extension period (BEP) and open-label extension (OLE) period]
- Safety Follow-Up period (40 weeks)
Tipo de estudio
Intervencionista
Inscripción (Estimado)
195
Fase
- Fase 3
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: Dianthus Clinical Contact Center
- Número de teléfono: 929-999-4055
- Correo electrónico: clinicaltrials@dianthustx.com
Ubicaciones de estudio
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Florida
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Boca Raton, Florida, Estados Unidos, 33432
- Reclutamiento
- Cinical Study Site
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North Carolina
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Fayetteville, North Carolina, Estados Unidos, 28304
- Aún no reclutando
- Cinical Study Site
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Texas
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Houston, Texas, Estados Unidos, 77009
- Reclutamiento
- Cinical Study Site
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-
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:
- Must have given written informed consent before any study-related activities are carried out
- Weight range between 40-130 kg at Screening
Diagnosis of gMG by the following tests:
- Acetylcholine receptor antibody (AChR Ab) positive, and
- One of the following:
i. History of abnormal neuromuscular transmission test; ii. History of positive anticholinesterase test; iii. Clinical response to acetylcholinesterase inhibitors.
- Myasthenia Gravis Foundation of America (MGFA) Class II-IVa
- MG-ADL scale score of 6 or more
- QMG scale score of 10 or more
- Documented vaccinations against encapsulated bacteria in accordance with local requirements and based on vaccine availability
- Female participants must be of non-childbearing potential, or if of childbearing potential, must agree not to donate ova, not to attempt to become pregnant and, if engaging in sexual intercourse with a male partner, must agree to use a highly effective method of contraception
- Male participants agree not to donate sperm and, if engaging in sexual intercourse with a female partner who could become pregnant, must agree to use an acceptable method of contraception
Exclusion Criteria:
- History or presence of significant medical/surgical condition including any acute illness, mental illness, or major surgery considered to be clinically significant or that could have potential impact on safety/efficacy or study procedures
- Known complement deficiency
- Prior history (at any time) of N. meningitidis infection
- Participants with known seropositivity or who test positive for an active viral infection with human immunodeficiency virus (HIV-1 or HIV-2), hepatitis B (HBV; except participants who are seropositive because of HBV vaccination) or hepatitis C virus (HCV) during Screening
- Previous treatment with claseprubart (DNTH103) or participation in a clinical trial with claseprubart. [
- Any thymic surgery/biopsy within 1 year of Screening
- Any known or untreated thymoma.
- Any history of thymic carcinoma or thymic malignancy
- History of active malignancy within 5 years prior to Screening, except basal cell carcinoma of the skin, curatively resected squamous cell carcinoma of the skin, cervical carcinoma in situ curatively treated or low-grade prostate adenocarcinoma for which appropriate management is observation alone
Concurrent or previous use of the following medication within the time periods specified below.
- Rituximab or other B-cell targeting therapies (ie, inebilizumab) within 6 months (180 days) prior to randomization (Day 1);
- Intravenous immunoglobulin (IVIg) and plasma exchange (PLEX) within 4 weeks (28 days) prior to randomization (Day 1)
- Participation in another clinical study of an investigational drug within 90 days or 5 half-lives of the investigational agent
- Diagnosis of systemic lupus erythematosus (SLE) or family history (defined as a parent, sibling, or child) of SLE
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: Cuadruplicar
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Comparador de placebos: Placebo
Intravenous (IV) infusion of Placebo on Day 1 followed by subcutaneous (SC) injections of Placebo every 2 weeks (Q2W) starting at Week 1 (Day 8).
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IV infusion on Day 1
Prefilled syringe containing placebo for SC administration
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Experimental: Claseprubart Q2W
IV loading dose of claseprubart on Day 1 followed by SC injections of claseprubart Q2W starting at Week 1 (Day 8).
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IV loading dose on Day 1
Otros nombres:
Prefilled syringe containing claseprubart for SC administration
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Experimental: Claseprubart Every 4 weeks (Q4W)
IV loading dose of claseprubart on Day 1 followed by SC injections of claseprubart or Placebo Q2W starting at Week 1 (Day 8), with doses alternating between claseprubart and placebo.
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Prefilled syringe containing placebo for SC administration
IV loading dose on Day 1
Otros nombres:
Prefilled syringe containing claseprubart for SC administration
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Change from Baseline to Week 17 in Myasthenia Gravis Activities of Daily Living (MG-ADL) Scale Score
Periodo de tiempo: Baseline (Day 1) to Week 17
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The MG-ADL score is an 8-item patient reported outcome (PRO) instrument.
The MG-ADL targets symptoms of disability across ocular, bulbar, respiratory, and axial symptoms.
The item responses are scored from 0 to 3, and the total score of the MG-ADL is the sum of the 8 items and ranges from 0 to 24, with a higher score indicating more disability.
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Baseline (Day 1) to Week 17
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Change from Baseline to Week 17 in Quantitative Myasthenia Gravis (QMG) Scale Score
Periodo de tiempo: Baseline (Day 1) to Week 17
|
The QMG is a clinician-reported assessment to evaluate muscle strength.
The QMG consists of 13 items that measure endurance or fatiguability, with each item having a possible score that ranges from 0 - 3. The total possible QMG scores range from 0 - 39, with a higher score indicating greater disease burden.
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Baseline (Day 1) to Week 17
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Change from Baseline to Week 17 in Myasthenia Gravis Composite (MGC) Scale Score
Periodo de tiempo: Baseline (Day 1) to Week 17
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The MGC is a validated assessment tool for measuring clinical status of participants with MG.
The range of total MGC score is 0 to 50, with higher scores indicating more severe disease.
A clinically meaningful improvement is reflected by a 3-point improvement in MGC score.
The MGC assesses 10 important functional areas most frequently affected by MG and the scales are weighted for clinical significance that incorporates patient-reported outcomes.
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Baseline (Day 1) to Week 17
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Proportion of Participants with Greater Than or Equal to (≥) a 5-point Reduction in MG-ADL Scale Score at Week 17 Compared to Baseline
Periodo de tiempo: Baseline (Day 1) to Week 17
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Baseline (Day 1) to Week 17
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Proportion of Participants Who Reach Minimal Symptom Expression (MSE), Defined as MG-ADL 0 or 1 at Week 17, Without Use of Rescue Therapy
Periodo de tiempo: Baseline (Day 1) to Week 17
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Baseline (Day 1) to Week 17
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Proportion of Participants with a ≥ 5-point Reduction in QMG Scale Score at Week 17 Compared to Baseline
Periodo de tiempo: Baseline (Day 1) to Week 17
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Baseline (Day 1) to Week 17
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Incidence of Treatment-emergent Adverse Events (TEAEs) and Treatment-Emergent and Treatment-Emergent Serious Adverse Events (SAEs) in the RCT period, BEP, OLE, and Safety Follow-Up
Periodo de tiempo: Baseline (Day 1) through Safety Follow-Up period (up to approximately 161 weeks)
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Number of participants with TEAEs and treatment-emergent SAEs will be reported.
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Baseline (Day 1) through Safety Follow-Up period (up to approximately 161 weeks)
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Serum Concentrations of Claseprubart
Periodo de tiempo: Baseline (Day 1) through Safety Follow-Up period (up to approximately 161 weeks)
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Blood samples will be collected for measurement of serum concentrations of claseprubart at various timepoints both pre- and post-dose.
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Baseline (Day 1) through Safety Follow-Up period (up to approximately 161 weeks)
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Change from Baseline in Complement Total Blood Test (CH50) in Serum ex vivo
Periodo de tiempo: Baseline (Day 1) through Safety Follow-Up period (up to approximately 161 weeks)
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Blood samples will be collected to determine changes in CH50 at various timepoints.
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Baseline (Day 1) through Safety Follow-Up period (up to approximately 161 weeks)
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Incidence of Antidrug Antibody (ADAs) Against Claseprubart in the RCT Period, BEP, OLE, and Safety Follow-Up
Periodo de tiempo: Baseline (Day 1) through Safety Follow-Up period (up to approximately 161 weeks)
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Blood samples will be collected to measure ADA against claseprubart at various timepoints.
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Baseline (Day 1) through Safety Follow-Up period (up to approximately 161 weeks)
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Titer of ADAs Against Claseprubart in the RCT Period, BEP, OLE, and Safety Follow-Up
Periodo de tiempo: Baseline (Day 1) through Safety Follow-Up period (up to approximately 161 weeks)
|
Blood samples will be collected to measure ADA against claseprubart at various timepoints.
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Baseline (Day 1) through Safety Follow-Up period (up to approximately 161 weeks)
|
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 (Actual)
29 de junio de 2026
Finalización primaria (Estimado)
1 de diciembre de 2028
Finalización del estudio (Estimado)
1 de septiembre de 2031
Fechas de registro del estudio
Enviado por primera vez
27 de mayo de 2026
Primero enviado que cumplió con los criterios de control de calidad
9 de junio de 2026
Publicado por primera vez (Actual)
15 de junio de 2026
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
1 de septiembre de 2026
Última actualización enviada que cumplió con los criterios de control de calidad
28 de agosto de 2026
Última verificación
1 de junio de 2026
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
- Enfermedades del Sistema Nervioso
- Neoplasias por sitio
- Neoplasias
- Enfermedades Neuromusculares
- Enfermedades autoinmunes
- Enfermedades del sistema inmunológico
- Enfermedades Autoinmunes del Sistema Nervioso
- Enfermedades neurodegenerativas
- Síndromes Paraneoplásicos Del Sistema Nervioso
- Neoplasias del Sistema Nervioso
- Síndromes paraneoplásicos
- Enfermedades de la unión neuromuscular
- Miastenia gravis
Otros números de identificación del estudio
- DNTH103-MG-301
- 2026-525298-38-00 (Ctis)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
NO
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. .