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Estudio de fase 2, aleatorizado, en doble ciego y controlado con placebo de HepTcell (FP-02.2 potenciada) como vacuna inmunoterapéutica en pacientes con hepatitis B crónica inactiva no tratados previamente

  • Protocol code: ALT-301-202
  • EudraCT code: 2020-002118-42
  • Pathology: Certes malalties infeccioses i parasitàries
  • Principal investigator:  Buti Ferret, Maria
  • Research group:  Malalties hepàtiques
  • Service: Hepatologia
  • Phase: Fase II
  • Recruiting: Open
  • Status: Iniciat

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Controller: Fundació Hospital Universitari Vall Hebron Institut de Recerca – VHIR- G60594009.
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Data retention time: As long as they are useful for the purpose for which they were collected and responsibilities may arise.
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 fase III multicéntrico, aleatorizado, doble ciego, con doble enmascaramiento y grupos paralelos para evaluar la eficacia y seguridad de fenebrutinib comparado con ocrelizumab en pacientes adultos con esclerosis múltiple primaria progresiva.

  • Protocol code: GN41791
  • EudraCT code: 2019-003919-53
  • Pathology: Malalties del sistema nerviós
  • Principal investigator:  Montalban Gairín, Xavier
  • Research group:  Neuroimmunologia clínica
  • Service: Neuroimmunologia
  • Phase: Fase III
  • Recruiting: Open
  • Status: Open

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Controller: Fundació Hospital Universitari Vall Hebron Institut de Recerca – VHIR- G60594009.
Purpose: Request for information on VHIR clinical research.
Legitimation: Your consent. The data requested is necessary and your request cannot be processed if you do not provide them.
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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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A multi-center, open-label, uncontrolled, single-arm, extension study to determine the long-term safety and tolerability of oral lucerastat in adult subjects with Fabry disease

  • Protocol code: ID-069A302
  • EudraCT code: 2018-002210-12
  • Pathology: Nervous system diseases
  • Principal investigator:  Camprodon Gomez, Maria
  • Research group:  Malalties neurodegeneratives
  • Service: Medicina Interna
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Controller: Fundació Hospital Universitari Vall Hebron Institut de Recerca – VHIR- G60594009.
Purpose: Request for information on VHIR clinical research.
Legitimation: Your consent. The data requested is necessary and your request cannot be processed if you do not provide them.
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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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Comprehensive assessment of erenumab efficacy in subjects with high frequency episodic migraine with at least 1 previously failed preventive treatment: a clobal, double-blind, placebo-controlled phase 4 study.

  • Protocol code: 20190008
  • EudraCT code: 2019-003646-33
  • Pathology: Nervous system diseases
  • Principal investigator:  Pozo Rosich, Patricia
  • Research group:  Cefalea i dolor neurològic
  • Service: Neurologia
  • Phase: Fase IV
  • Recruiting: Open
  • Status: Open

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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 multicéntrico aleatorizado, doble ciego, controlado con placebo y de grupos paralelos acerca de CVL-865 como tratamiento complementario en adultos con crisis convulsivas de inicio focal resistentes a los fármacos.

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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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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 
The request for information on a research project or clinical trial does not entail inclusion in it.

Ensayo de fase III, doble ciego, aleatorizado, controlado con placebo, de grupos paralelos, de dosis flexible y de 27 semanas para evaluar la eficacia, la seguridad y la tolerabilidad de TAVAPADÓN en la Enfermedad de Parkinson Precoz. (Ensayo TEMPO-2)

  • Protocol code: CVL-751-PD-002
  • EudraCT code: 2019-002950-22
  • Pathology: Nervous system diseases
  • Principal investigator:  Hernández Vara, Jorge
  • Research group:  Neurodegenerative Diseases
  • Service: Neurology
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Controller: Fundació Hospital Universitari Vall Hebron Institut de Recerca – VHIR- G60594009.
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IMPACTO DE DAPAGLIFOZINA EN EL REMODELADO AURICULAR DE PACIENTES CON INSUFICIENCIA CARDIACA: MODA study

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“Estudio de Fase III, Abierto y Multicéntrico para Evaluar la Eficacia y Seguridad de Darvadstrocel en el Tratamiento de la Fístula Perianal Compleja en Población Pediátrica con Enfermedad de Crohn Durante 24 Semanas y un período de seguimiento extendido de hasta 52 semanas”

  • Protocol code: Darvadstrocel-3004
  • EudraCT code: 2020-003193-48
  • Pathology: Malalties del sistema digestiu
  • Principal investigator:  Segarra Canton, Oscar
  • Service: Pediatria General i Especialitats
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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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 de fase iiib, multicéntrico, aleatorizado, doble ciego y controlado para evaluar la eficacia, la seguridad y la farmacocinética de una dosis más alta de ocrelizumab en adultos con esclerosis múltiple primaria progresiva

  • Protocol code: BN42083
  • EudraCT code: 2020-000894-26
  • Pathology: Nervous system diseases
  • Principal investigator:  Montalban Gairín, Xavier
  • Research group:  Clinical Neuroimmunology
  • Service: Neuroimmunology
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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ESTUDIO DE CONTINUACIÓN ABIERTO Y MULTICÉNTRICO PARA EVALUAR LASEGURIDAD, LA TOLERABILIDAD Y LA EFICACIA DE LA ADMINISTRACIÓN A LARGOPLAZO DE GANTENERUMAB EN PARTICIPANTES CON ENFERMEDAD DEALZHEIMER

  • Protocol code: WN42171
  • EudraCT code: 2020-000766-42
  • Pathology: Nervous system diseases
  • Principal investigator:  Pujadas Navinés, Francesc
  • Service: Neurology
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Estudio multicéntrico, aleatorizado, doble ciego y de grupos paralelos para evaluar la eficacia, seguridad y tolerabilidad de una terapia de combinación con tropifexor (LJN452) y licogliflozina (LIK066) por vía oral, en comparación con cada uno de ellos en monoterapia, para el tratamiento de pacientes adultos con esteatohepatitis no alcohólica (EHNA) y fibrosis hepática (ELIVATE).

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Ensayo en fase 3, abierto, de grupo único y multicéntrico, para evaluar la seguridad a largo plazo de octreotida (CAM2029) subcutánea de liberación prolongada en pacientes con acromegalia

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Eficacia y tolerabilidad de 4 semanas de tedizolid en infecciones protésicas articulares tratadas con retirada del implante (PROTEDI)

  • Protocol code: PROTEDI
  • EudraCT code: 2018-002465-18
  • Pathology: Certain infectious and parasitic diseases
  • Principal investigator:  Rodríguez Pardo, Ma Dolores
  • Research group:  Malalties infeccioses
  • Service: Infeccioses
  • Phase: Phase IV
  • Recruiting: Open
  • Status: Open

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Ultrasonido sinovial como resultado principal en un estudio internacional, multicéntrico, aleatorizado, abierto de 3 brazos, con control activo de grupos paralelos, comparando baricitinib solo y combinado con metotrexato frente a un inhibidor TNF-A en pacientes con artritis reumatoide: Buscando predictores sinoviales de respuesta.

  • Protocol code: BIOP-US/I4V-XM-O0003
  • EudraCT code: 2018-004558-30
  • Principal investigator:  De Agustin De Oro, Juan Jose
  • Research group:  Reumatologia
  • Service: Reumatologia
  • Phase: Phase IV
  • Recruiting: Open
  • Status: Open

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Ensayo de fase III, doble ciego, aleatorizado, controlado con placebo, de grupos paralelos, de dosis flexible y de 27 semanas para evaluar la eficacia, la seguridad y la tolerabilidad de tavapadón como tratamiento adyuvante para la enfermedad de Parkinson en adultos tratados con levodopa con fluctuaciones motrices (ensayo TEMPO-3)

  • Protocol code: CVL-751-PD-003
  • EudraCT code: 2019-002951-40
  • Pathology: Nervous system diseases
  • Principal investigator:  Hernández Vara, Jorge
  • Research group:  Neurodegenerative Diseases
  • Service: Neurology
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Estudio global en fase III,, aleatorizado, doble ciego y controlado con placebo para evaluar la eficacia y la seguridad de ION-682884 en pacientes con miocardiopatía amiloide por transtiretina (MC-ATTR)

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Estudio en Fase 3, de 12 meses de tratamiento abierto con Lasmiditan en pacientes pediátricos con migraña

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Tenecteplasa en comparación con Alteplasa para pacientes con oclusión de gran vaso antes de la trombectomía.

  • Protocol code: TNKCAT
  • EudraCT code: 2020-001599-13
  • Pathology: Nervous system diseases
  • Principal investigator:  Rubiera Del Fueyo, Marta Aurora
  • Research group:  Recerca en ictus
  • Service: Neurology
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Estudio de eficacia y seguridad de fase 3, aleatorizado y doble ciego que compara SAR442168 con teriflunomida (Aubagio®) en participantes con formas recidivantes de esclerosis múltiple

  • Protocol code: EFC16033
  • EudraCT code: 2020-000637-41
  • Pathology: Nervous system diseases
  • Principal investigator:  Montalban Gairín, Xavier
  • Research group:  Clinical Neuroimmunology
  • Service: Neuroimmunology
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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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 
The request for information on a research project or clinical trial does not entail inclusion in it.

Estudio doble ciego, aleatorizado y controlado con placebo para evaluar la eficacia y la seguridad de odevixibat (A4250) en niños con atresia biliar que se han sometido a hepatoportoenterostomía de Kasai (BOLD)

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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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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 
The request for information on a research project or clinical trial does not entail inclusion in it.