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Estudio de extensión abierto y no aleatorizado para evaluar la eficacia, seguridad y tolerabilidad a largo plazo de LNP023 en sujetos con glomerulopatía C3.

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Controller: Fundació Hospital Universitari Vall Hebron Institut de Recerca – VHIR- G60594009.
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Ensayo multicéntrico, aleatorizado, con doble enmascaramiento, controlado con placebo y con producto activo, para evaluar la eficacia de la monoterapia con brexpiprazol para el tratamiento de adolescentes (de 13 a 17 años) con esquizofrenia.

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Controller: Fundació Hospital Universitari Vall Hebron Institut de Recerca – VHIR- G60594009.
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Estudio abierto, de seguridad a largo plazo, de tolerabilidad y de eficacia de GIVINOSTAT en todos los pacientes con DMD que hayan sido tratadospreviamente en uno de los estudios de GIVINOSTAT.

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Controller: Fundació Hospital Universitari Vall Hebron Institut de Recerca – VHIR- G60594009.
Purpose: Request for information on VHIR clinical research.
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ESTUDIO MULTICÉNTRICO DE FASE 2B, ALEATORIZADO DOBLE CIEGO, CONTROLADO CON PLACEBO, DE BÚSQUEDA DE DOSIS PARA EVALUAR EL PERFIL DE EFICACIA Y SEGURIDAD DE PF-06700841 EN PARTICIPANTES CON LUPUS ERITEMATOSO SISTÉMICO (LES) ACTIVO

  • Protocol code: B7931028
  • EudraCT code: 2018-004175-12
  • Principal investigator:  Cortes Hernandez, Josefina
  • Research group:  Reumatologia
  • Service: Reumatologia
  • Phase: Phase II
  • Recruiting: Open
  • Status: Open

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Controller: Fundació Hospital Universitari Vall Hebron Institut de Recerca – VHIR- G60594009.
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Estudio aleatorizado, doble ciego, controlado con placebo, multicéntrico, para evaluar la seguridad, la tolerabilidad y la eficacia del XEN1101 como tratamiento adyuvante en la epilepsia de inicio focal

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Controller: Fundació Hospital Universitari Vall Hebron Institut de Recerca – VHIR- G60594009.
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Rights: You can access, rectify, delete your data, oppose or limit its processing and request its portability, as well as revoke your consent without retroactive effects by contacting lopd@vhir.org. The revocation of consent and the opposition to the processing of your data will prevent the purpose from being carried out. DPO: dpd@ticsalutsocial.org. More information 
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Estudio en fase 1b que investiga la seguridad, la tolerabilidad y la eficacia de PP353 en el tratamiento de pacientes con dolor lumbar crónico asociado a edema óseo en la placa terminal del cuerpo de la vértebra (Modic 1).

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Controller: Fundació Hospital Universitari Vall Hebron Institut de Recerca – VHIR- G60594009.
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The request for information on a research project or clinical trial does not entail inclusion in it.

Estudio clínico en fase III/IV multinacional, multicéntrico, con doble enmascaramiento y controlado por placebo para evaluar la eficacia y la seguridad de Aramchol en pacientes con esteatohepatitis no alcohólica (EHNA) Estudio ARMOR

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Estudio en fase III, multicéntrico, aleatorizado, doble ciego, de 52 semanas de duración, para comparar la eficacia y la seguridad de GSK3196165 con placebo y con tofacitinib, en combinación con FARME sintéticos convencionales, en participantes con artritis reumatoide con actividad de moderada a intensa que han obtenido una respuesta inadecuada a los FARME sintéticos convencionales o a los biológicos.

  • Protocol code: 201791
  • EudraCT code: 2019-000867-26
  • Principal investigator:  Marsal Barril, Sara
  • Research group:  Rheumatology
  • Service: Rheumatology
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Ensayo de fase III controlado con placebo, de un año de duración, para evaluar la eficacia y seguridad de la inmunoterapia sublingual en comprimidos frente a ácaros del polvo doméstico en niños (de 5-11 años de edad) con rinitis/rinoconjuntivitis alérgica inducida por ácaros del polvo doméstico, con o sin asma.

  • Protocol code: MT-12
  • EudraCT code: 2019-000560-22
  • Pathology: Símptomes, signes i troballes anormals clíniques i de laboratori, no classificades enlloc més
  • Principal investigator:  Garriga Baraut, Maria Teresa
  • Research group:  Creixement i desenvolupament
  • Service: General Pediatrics and Specialties
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Fase 1B de crizotinib en combinación o como agente único en pacientes pediátricos con tumores malignos positivos para ALK, ROS1 o MET

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A Phase 3, Open-label Study Evaluating the Long-term Safety and Efficacy of VX-445 Combination Therapy in Subjects With Cystic Fibrosis Who Are Heterozygous for the F508del Mutation and a Gating or Residual Function Mutation (F/G and F/RF Genotypes)

  • Protocol code: VX18-445-110
  • EudraCT code: 2019-000833-37
  • Principal investigator:  Álvarez Fernandez, Antonio
  • Research group:  Pneumologia
  • Service: Pneumologia
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Estudio multicéntrico para evaluar la seguridad y tolerabilidad a largo plazo de un tratamiento en abierto con sacubitrilo/valsartán en pacientes pediátricos con insuficiencia cardíaca debida a disfunción sistólica de ventrículo izquierdo sistémico, que han completado el estudio CLCZ696B2319 (PANORAMA-HF)

  • Protocol code: CLCZ696B2319E1
  • EudraCT code: 2018-004154-25
  • Principal investigator:  Gran Ipiña, Ferran
  • Research group:  Malalties cardiovasculars
  • Service: Cardiologia Pediàtrica
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Estudio en fase III, multicéntrico, aleatorizado, abierto y controlado con principio activo de DS-8201a, un conjugado de fármaco y anticuerpo (CAF) anti-HER2, en comparación con el tratamiento elegido por el médico en sujetos con cáncer de mama irresecable o metastásico (o ambos) con expresión baja de HER-2

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A Phase 3, Open-label Study Evaluating the Long-term Safety of VX-445 Combination Therapy in Subjects With Cystic Fibrosis

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Estudio de extensión a largo plazo de seguridad y eficacia de SAR442168 en participantes con esclerosis múltiple recurrente

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Efectos de semaglutida a largo plazo en la retinopatía diabetic en sujectos con diabetes tipo 2

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Estudio de fase 1 en el que se evalúa LY3295668 erbumina (un inhibidor de la cinasa Aurora A) en monoterapia y en politerapia en pacientes con neuroblastoma recidivante o resistente al tratamiento

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A Phase 2 Open-Label Study of Continuation Treatment With Combination Pyrimidine Nucleosides in Patients With Thymidine Kinase 2 Deficiency (TK2)

  • Protocol code: MT-1621-102
  • EudraCT code: 2018-004277-27
  • Principal investigator:  Munell Casadesus, Francina
  • Research group:  Pediatric Neurology
  • Service: General Pediatrics and Specialties
  • Phase: Phase II
  • Recruiting: Open
  • Status: Open

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Ensayo multicéntrico, aleatorizado, doble ciego, con grupos paralelos y controlado con placebo para investigar el uso de benralizumab en la esofagitis eosinofílica (MESSINA)

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Ensayo Clínico en fase 3, aleatorizado, doble ciego, controlado con placebo, ulticéntrico, para evaluar la eficacia y seguridad de octreotida subcutánea de liberación prolongada (CAM2029) en pacientes con acromegalia

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