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Estudio en fase IIIb, abierto, para evaluar la eficacia y seguridad a largo plazo del tratamiento combinado de elexacaftor/tezacaftor/ivacaftor en pacientes con fibrosis quística de 6 años de edad en adelante heterocigotos para la mutación F508del y una mutación mínima de la función (F/MF)

  • Protocol code: VX20-445-119
  • EudraCT code: 2020-001404-42
  • Pathology: Símptomes, signes i troballes anormals clíniques i de laboratori, no classificades enlloc més
  • Principal investigator:  GARTNER TIZZANO, SILVIA
  • Research group:  Creixement i desenvolupament
  • Service: Obstetrícia
  • Phase: Fase III
  • Recruiting: Open
  • Status: Iniciat

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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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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 de fase II, aleatorizado, abierto y controlado para evaluar la eficacia y seguridad de la combinación de tocilizumab con pembrolizumab (MK-3475) en pacientes con neumonía causada por coronavirus 2019 (COVID-19)

  • Protocol code: MedOPP376
  • EudraCT code: 2020-001160-28
  • Pathology: Certes malalties infeccioses i parasitàries
  • Principal investigator:  González Fernández, Antonio
  • Research group:  Malalties sistèmiques
  • Service: Medicina Interna
  • Phase: Fase II
  • Recruiting: Closed
  • Status: Open

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Estudio en fase II, multicéntrico, aleatorizado, doble ciego y controlado con placebo con tratamiento activo diferido para investigar la eficacia, la seguridad y la farmacocinética de JNJ-73763989 + análogos de los nucleós(t)idos en participantes coinfectados por el virus de la hepatitis B y la hepatitis D..

  • Protocol code: 73763989HPB2004
  • EudraCT code: 2020-001249-37
  • Pathology: Certain infectious and parasitic diseases
  • Principal investigator:  Buti Ferret, Maria
  • Research group:  Malalties hepàtiques
  • Service: Hepatologia
  • Phase: Phase II
  • Recruiting: Open
  • Status: Open

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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: Certain infectious and parasitic diseases
  • Principal investigator:  Buti Ferret, Maria
  • Research group:  Liver Diseases
  • Service: Hepatology
  • Phase: Phase II
  • Recruiting: Open
  • Status: Open

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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: Phase III
  • Recruiting: Open
  • Status: Open

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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: Internal Medicine
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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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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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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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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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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Controller: Fundació Hospital Universitari Vall Hebron Institut de Recerca – VHIR- G60594009.
Purpose: Request for information on VHIR clinical research.
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Transfers: Your data will not be transferred to third parties except to the Principal Investigator who leads the research in order to be able to respond to your query.
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 
The request for information on a research project or clinical trial does not entail inclusion in it.

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

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CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.

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.
Transfers: Your data will not be transferred to third parties except to the Principal Investigator who leads the research in order to be able to respond to your query.
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 
The request for information on a research project or clinical trial does not entail inclusion in it.