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Multi-Omic SignAtures of Inflammatory Cutaneous Diseases (MOSAIC)

13 de agosto de 2026 actualizado por: Guy's and St Thomas' NHS Foundation Trust

The goal of this observational study is to identify the immune profile underlying various inflammatory skin diseases, through multi-omic procedures.

The main questions it aims to answer are:

  1. What are the molecular and immune signatures of individuals with inflammatory skin disease?
  2. Can these signatures reveal potential therapeutic targets for individuals with inflammatory skin disease?
  3. How do patients' multi-omic signatures change before and after receiving systemic therapy?
  4. Can the samples and data collected through this study provide a valuable bioresource for future skin disease research?

Descripción general del estudio

Estado

Aún no reclutando

Descripción detallada

MOSAIC (Multi-Omic Signatures of Inflammatory Cutaneous Diseases) is a non-commercial, investigator-led, single-centre, prospective observational cohort study. Participants will be recruited at Guy's and St Thomas' NHS Foundation Trust, with University Hospitals Birmingham acting as a participant identification centre. The study will investigate individuals with a broad range of common and rare inflammatory skin diseases, including genetic skin diseases such as epidermolysis bullosa, alongside a healthy comparison cohort.

The study is based on the hypothesis that inflammatory skin diseases may share identifiable molecular and immune pathways, despite differences in their clinical presentation and underlying causes. By integrating molecular data with detailed clinical information, MOSAIC aims to identify and characterise disease-associated immune signatures, distinguish molecular subgroups or "endotypes", and identify potentially druggable pathways. The study will also investigate how molecular and immune profiles change following systemic treatment and will establish a well-characterised biological resource for future skin disease research. MOSAIC is observational: no treatment will be assigned or administered as part of the study, and participants will continue to receive clinical care according to usual practice.

Participants will undergo a detailed baseline assessment. Clinical information will include demographic characteristics, medical and family history, disease phenotype and duration, previous and current treatments, concomitant conditions and medications, relevant environmental factors, clinical assessments, patient- and clinician-reported information, and medical photography where applicable. Healthy participants will provide comparison data and samples at a single baseline visit.

Biological samples collected at baseline may include routine clinical blood samples, research blood samples and skin biopsies. Research blood will be used to isolate DNA, RNA, serum, plasma and peripheral blood mononuclear cells. Patients may provide samples from lesional and non-lesional skin, while healthy participants will provide site-matched control samples where possible. Subject to separate consent and clinical relevance, optional samples may include skin or mucosal swabs, stool, mucosal biopsies, scalp biopsies and skin that would otherwise be discarded during surgery. Relevant historical results obtained within six months before the baseline visit may be used where scientifically and clinically appropriate to reduce unnecessary repeat invasive procedures.

Patients who start, switch or stop a systemic therapy, or who experience a worsening of their disease, may be invited to attend optional longitudinal follow-up visits if they are not participating in another interventional study. Up to five optional follow-up visits may take place at clinically and scientifically relevant time points, such as Day 3, Week 1, Week 16, Month 6 and Month 12. The timing may be adapted according to the mechanism of the treatment or the specific research question. Follow-up assessments may include updated clinical and treatment information, examination, disease-specific assessments, medical photography and repeat collection of research samples. This will allow molecular profiles before and after treatment, or during changes in disease activity, to be compared. Clinical outcome information may be followed for up to five years after sampling to support longer-term correlation with molecular findings.

Samples may undergo single or multiple complementary analyses. These may include DNA sequencing and genotyping; epigenetic analysis; bulk, single-cell and spatial transcriptomics; NanoString profiling; proteomic, cytokine and metabolomic analysis; flow, spectral, imaging or mass cytometry; and functional ex vivo assays. Skin samples may also undergo histology, immunostaining, immunofluorescence, confocal imaging and cell-isolation procedures. Where appropriate, cells may be used in in vitro cultures, three-dimensional organotypic models, spheroids or organoids. Skin, mucosal and stool samples may also be analysed to characterise microbial composition and function. Multi-omic data will be integrated with clinical phenotype, disease activity, treatment exposure and longitudinal clinical information to identify shared and disease-specific pathways and potential therapeutic targets.

Participants found to have potentially actionable or druggable immune profiles may, with appropriate consent, be approached about separate interventional clinical trials. For example, eligible participants with epidermolysis bullosa may be considered for ART-EB, a separate clinical trial evaluating repurposed biological therapies. Molecular profiles generated through MOSAIC may be used as baseline information to support biological stratification and treatment matching in such studies. Participation in MOSAIC does not guarantee eligibility for, or entry into, an interventional trial, and separate informed consent will be required.

The planned case-to-control ratio prioritises the characterisation of heterogeneous inflammatory skin diseases while maintaining a feasible healthy comparison group. The protocol estimates that 300 inflammatory skin disease cases will provide approximately 84% power, using a two-sided 5% significance level, to identify a small-to-moderate effect across four disease subcategories, represented by a Cohen's w of 0.2. A subgroup of 100 cases would provide similar power to detect a larger effect of approximately Cohen's w 0.35 across four subcategories.

A detailed Statistical Analysis Plan will be prepared by the study statistician and finalised before database lock. Analyses will be tailored to the relevant clinical or molecular research question and may include parametric and non-parametric comparisons, linear or logistic regression, interaction testing, subgroup analyses and longitudinal analyses. These analyses will examine relationships between multi-omic signatures, clinical phenotypes, treatment exposure and changes over time.

Tipo de estudio

De observación

Inscripción (Estimado)

400

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

Copia de seguridad de contactos de estudio

  • Nombre: Clinical Trial Manager
  • Número de teléfono: 53378 +44 20 7188 7188
  • Correo electrónico: rashida.pramanik@nhs.net

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

Sí

Método de muestreo

Muestra no probabilística

Población de estudio

Dermatology clinics (Guys and St Thomas' Hospital and University Hospitals Birmingham) and community (healthy volunteers)

Descripción

Inclusion Criteria:

  • Able to provide written informed consent prior to performing any protocol-related procedures, including screening.
  • Adults (≥18 years) with confirmed diagnosis of inflammatory skin disease (defined as any skin disease with an inflammatory component, including but not limited to, genetic skin disease, such as EB), OR
  • Adults age (≥18 years) without skin or systemic disease.

Exclusion Criteria:

  • Inability to give written informed consent.
  • Participants who have received topical corticosteroids to sites of biopsies (inflamed area of skin) for at least 2 weeks prior to tissue sampling.
  • Inability to participate in study-specific procedures.
  • Participants who are pregnant (confirmed on a positive urine pregnancy test) or breastfeeding
  • Enrolment in any interventional study with systemic treatment within 3 months prior to baseline biopsy.

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

Cohortes e Intervenciones

Grupo / Cohorte
Healthy participants who do not have an inflammatory skin condition
Participants with an inflammatory skin condition

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
DLQI
Periodo de tiempo: Baseline and Day 3, Week 1, Week 16, Month 6, Month 12
Dermatology Quality of Life Index
Baseline and Day 3, Week 1, Week 16, Month 6, Month 12

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
EBDASI
Periodo de tiempo: Baseline and Day 3, Week 1, Week 16, Month 6, Month 12
Epidermolysis Bullosa Disease Activity and Scarring Index
Baseline and Day 3, Week 1, Week 16, Month 6, Month 12
iscorEB
Periodo de tiempo: Baseline and Day 3, Week 1, Week 16, Month 6, Month 12
Instrument for Scoring Clinical Outcomes of Research for Epidermolysis Bullosa
Baseline and Day 3, Week 1, Week 16, Month 6, Month 12
LIS
Periodo de tiempo: Baseline and Day 3, Week 1, Week 16, Month 6, Month 12
Leuven Itch Scale
Baseline and Day 3, Week 1, Week 16, Month 6, Month 12
QOLEB
Periodo de tiempo: Baseline and Day 3, Week 1, Week 16, Month 6, Month 12
Quality of Life Evaluation in Epidermolysis Bullosa
Baseline and Day 3, Week 1, Week 16, Month 6, Month 12
WI-NRS
Periodo de tiempo: Baseline and Day 3, Week 1, Week 16, Month 6, Month 12
Worst Itch Numeric Rating Scale
Baseline and Day 3, Week 1, Week 16, Month 6, Month 12
GAD7
Periodo de tiempo: Baseline and Day 3, Week 1, Week 16, Month 6, Month 12
Generalised Anxiety Disorder Assessment
Baseline and Day 3, Week 1, Week 16, Month 6, Month 12
PHQ9
Periodo de tiempo: Baseline and Day 3, Week 1, Week 16, Month 6, Month 12
Patient Health Questionnaire-9
Baseline and Day 3, Week 1, Week 16, Month 6, Month 12
PASI
Periodo de tiempo: Baseline and Day 3, Week 1, Week 16, Month 6, Month 12
Psoriasis Area and Severity Index
Baseline and Day 3, Week 1, Week 16, Month 6, Month 12
PGA
Periodo de tiempo: Baseline and Day 3, Week 1, Week 16, Month 6, Month 12
Physician Global Assessment
Baseline and Day 3, Week 1, Week 16, Month 6, Month 12
BSA
Periodo de tiempo: Baseline and Day 3, Week 1, Week 16, Month 6, Month 12
Body Surface Area %
Baseline and Day 3, Week 1, Week 16, Month 6, Month 12
EASI
Periodo de tiempo: Baseline and Day 3, Week 1, Week 16, Month 6, Month 12
Eczema Area and Severity Index (EASI)
Baseline and Day 3, Week 1, Week 16, Month 6, Month 12
VAS
Periodo de tiempo: Baseline and Day 3, Week 1, Week 16, Month 6, Month 12
Visual Analog Scale
Baseline and Day 3, Week 1, Week 16, Month 6, Month 12

Colaboradores e Investigadores

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

Colaboradores

Investigadores

  • Investigador principal: Su M Lwin, MRCP (Derm) PhD BSc (Hons), King's College London

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 septiembre de 2026

Finalización primaria (Estimado)

1 de julio de 2031

Finalización del estudio (Estimado)

1 de julio de 2031

Fechas de registro del estudio

Enviado por primera vez

10 de agosto de 2026

Primero enviado que cumplió con los criterios de control de calidad

13 de agosto de 2026

Publicado por primera vez (Actual)

18 de agosto de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

18 de agosto de 2026

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

13 de agosto de 2026

Última verificación

1 de agosto de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

INDECISO

Información sobre medicamentos y dispositivos, documentos del estudio

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

No

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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