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Pharmacokinetics, Immunogenicity and Safety of Subcutaneous Dupilumab and Berahyaluronidase Alfa (ALT-B4) Coformulation (EXTENSA)

30 de octubre de 2026 actualizado por: Sanofi

A Randomized, Open-label, Multiple-dose Phase 3 Study to Evaluate Pharmacokinetics, Immunogenicity and Safety of Subcutaneous Dupilumab and Berahyaluronidase Alfa (ALT-B4) Coformulation Compared to the Approved Subcutaneous Dupilumab Formulation in Adults and Adolescents With Moderate-to-severe Atopic Dermatitis

This is a Phase 3, open label, randomized, parallel-group, 2-arm study. The purpose of this study is to measure PK, immunogenicity, safety and, tolerability of dupilumab hyaluronidase coformulation compared with dupilumab approved formulation in male or female participants with moderate-to-severe atopic dermatitis (AD) aged ≥12 years of age. Study details as follows:

  • The study duration includes screening period up to 4 weeks + treatment period of 20 weeks (± 3 days) and follow-up of 12 weeks (± 7 days).
  • The number of on-site visits will be 10 and one phone contact will be scheduled (during the follow-up period).

Descripción general del estudio

Estado

Aún no reclutando

Condiciones

Tipo de estudio

Intervencionista

Inscripción (Estimado)

150

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: Trial Transparency email recommended (Toll free for US & Canada)
  • Número de teléfono: option 6 800-633-1610
  • Correo electrónico: Contact-US@sanofi.com

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

12 años y mayores (Niño, Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Participant must be ≥12 years of age at the time of signing the informed consent.

  • Participants with chronic AD, (according to American Academy of Dermatology Consensus Criteria, that has been present for at least 12 months before the screening visit.

  • Participants with ≥10% body surface area (BSA) of AD involvement at the screening and baseline visits.

  • Participant's AD must be graded as Eczema Area and Severity Index (EASI) score ≥16 at the screening and baseline visits.

  • Validated Investigator Global Assessment for Atopic Dermatitis (v-IGA) ≥3 at the screening and baseline visits.

  • Worst-Itch Numerical Rating Scale (WI-NRS) weekly average score ≥4 in the 7 days before randomization.

  • Documented recent history (within 6 months before the screening visit) of inadequate response* to treatment with topical medications or for whom topical treatments are otherwise medically inadvisable (eg, because of important side effects or safety risks).

    *Inadequate response to topical therapy is defined as persistent moderate-to-severe AD (EASI ≥16, vIGA-AD ≥3, BSA ≥10%) despite ≥4 weeks of optimized topical anti-inflammatory treatment (medium/high potency corticosteroids ± calcineurin inhibitors), or documented intolerance/contraindication to such therapies.

  • For adolescents (≥12 and <18 years old) only, body weight ≥60 kg.

Exclusion Criteria:

  • Any history or presence of severe concomitant illness(es) that, in the Investigator's judgment, would adversely affect the participant's participation in the study. Examples include, but are not limited to participants with short life expectancy, participants with uncontrolled diabetes (hemoglobin A1c ≥9%), participants with cardiovascular conditions (e.g, cardiomyopathy, thromboembolism, Class III or IV cardiac failure according to the New York Heart Association classification), severe hematological conditions (e.g. hyperviscosity), severe renal conditions (e.g, participants on dialysis), hepato-biliary conditions (e.g, Child-Pugh class B or C), neurological conditions (e.g, demyelinating diseases), active major autoimmune diseases (e.g, lupus, inflammatory bowel disease, rheumatoid arthritis, etc), other severe endocrinological, gastrointestinal, metabolic, pulmonary, or lymphatic diseases. The specific justification for participants excluded under this criterion will be noted in study documents (chart notes, case report forms [CRF], etc).
  • Active chronic or acute infection requiring treatment with systemic antibiotics, antivirals, antiparasitics, antiprotozoals, or antifungals within 2 weeks before the baseline visit, or superficial skin infections within 1 week before the baseline visit. NOTE: participants may be rescreened after infection resolves.
  • Known or suspected history of immunosuppression, including history of invasive opportunistic infections (eg, tuberculosis [TB], histoplasmosis, listeriosis, coccidioidomycosis, pneumocystosis, aspergillosis) despite infection resolution: or unusually frequent, recurrent, or prolonged infections, suggesting immunocompromised status per Investigator judgment.
  • Presence of any skin comorbidities other than AD that, in the opinion of the Investigator, may interfere with the assessment of the study outcomes. For example: scabies, insect bite, folliculitis, lymphomatoid papulosis, chronic actinic dermatitis, dermatitis herpetiformis, sporotrichosis, bullous disease, or others.
  • History of malignancy within 5 years before the screening visit, except completely treated in situ carcinoma of the cervix, completely treated and resolved non-metastatic squamous or basal cell carcinoma of the skin.
  • Diagnosed with, suspected of, or at high risk for endoparasitic infection, and/or use of antiparasitic drugs within 2 weeks before Screening (Visit 1) or during the Screening period.
  • Previously treated with marketed dupilumab or having received dupilumab in a prior dupilumab clinical study.

The above information is not intended to contain all considerations relevant to a participant's potential participation in a clinical trial.

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: Dupilumab coformulated with berahyaluronidase alfa

dupilumab coformulated with berahyaluronidase alfa SC injection as per protocol

Pharmaceutical form: solution for injection Route of administration: SC injection

Otros nombres:
  • SAR231893 + ALT-B4
Comparador activo: Dupilumab approved formulation

Approved dupilumab SC injection as per protocol

Pharmaceutical form: solution for injection Route of administration: SC injection

Otros nombres:
  • SAR231893

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Ctrough,ss at Week 20
Periodo de tiempo: Week 20

Concentration observed before treatment administration during repeated dosing at steady state (SS).

Week 20

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
AUC0-4 weeks,ss
Periodo de tiempo: Week 0 through Week 4

Area under curve from time point 0 to 28 days at steady state

Week 0 through Week 4
Cmax,ss
Periodo de tiempo: Week 20

Maximum observed concentration during repeated dosing at steady state.

Week 20
Incidence of TEAEs, TE-AESIs, TE-SAEs, and TEAEs leading to permanent treatment discontinuation in the treatment-emergent period
Periodo de tiempo: Week 0 up to week 32

TEAEs: treatment-emergent adverse events TE-AESIs: treatment-emergent adverse events of special interest TE-SAE: treatment-emergent serious adverse events

Week 0 up to week 32
Incidence of potentially clinically significant abnormalities in laboratory test, vital signs, and ECGs abnormalities in the treatment-emergent period
Periodo de tiempo: Week 0 up to week 32
Week 0 up to week 32
Incidence of treatment-emergent anti-drug antibody (ADA) to dupilumab through Week 20
Periodo de tiempo: Week 0 up to week 20
Week 0 up to week 20
Incidence of treatment-emergent ADA to ALT-B4 through Week 20
Periodo de tiempo: Week 0 up to week 20
Week 0 up to week 20

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)

30 de noviembre de 2026

Finalización primaria (Estimado)

2 de mayo de 2028

Finalización del estudio (Estimado)

25 de julio de 2028

Fechas de registro del estudio

Enviado por primera vez

30 de octubre de 2026

Primero enviado que cumplió con los criterios de control de calidad

30 de octubre de 2026

Publicado por primera vez (Actual)

5 de noviembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

5 de noviembre de 2026

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

30 de octubre de 2026

Última verificación

1 de octubre de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

SÍ

Descripción del plan IPD

Qualified researchers may request access to patient level data and related study documents including the clinical study report, study protocol with any amendments, blank case report form, statistical analysis plan, and dataset specifications. Patient level data will be anonymized and study documents will be redacted to protect the privacy of trial participants. Further details on Sanofi's data sharing criteria, eligible studies, and process for requesting access can be found at: https://vivli.org

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. .

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