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GALACTIC-1 - Estudio de fase IIb, aleatorizado, doble ciego, multicéntrico, con grupos paralelos, controlado con placebo en pacientes con fibrosis pulmonaridiopática (FPI) para investigar la eficacia y la seguridad de TD139, un inhibidor de la galectina-3 inhalado administrado mediante un inhalador de polvo seco durante 52 semanas.

  • Protocol code: GALACTIC-1
  • EudraCT code: 2018-002664-73
  • Principal investigator:  Villar Gomez, Ana
  • Research group:  Pneumologia
  • Service: Pneumologia
  • Phase: Fase II
  • Recruiting: Open
  • Status: Iniciat

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ENSAYO FASE II DE BUSQUEDA DE DOSIS, MULTICENTRICO, ALEATORIZADO, CONTROLADO CON PLACEBO, DOBLE CIEGO Y DE GRUPOS PARALELOS, PARA EVALUAR LA EFICACIA Y LA SEGURIDAD DE DE BAY 2433334 EN PACIENTES DESPUÉS DE UN ICTUS AGUDO ISQUÉMICO NO CARDIO-EMBÓLICO. PACIFIC-STROKE

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Estudio global, multicéntrico, abierto, comparativo con controles históricos equiparables, de SHP611 intratecal en sujetos con leucodistrofia metacromática infantil tardía

  • Protocol code: SHP611-201
  • EudraCT code: 2018-003291-12
  • Principal investigator:  Del Toro Riera, Mireia
  • Research group:  Neurologia pediàtrica
  • Service: Pediatria General i Especialitats
  • Phase: Phase II
  • Recruiting: Open
  • Status: Open

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Ensayo clínico 3 que evalúa la isquemia perioperatoria

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Estudio en fase IV de 2 partes, multicéntrico, compuesto de una evaluación de optimización de la dosis de 1 año aleatorizada, doble ciego, de grupos paralelos, controlada con placebo y comparador activo, seguida de una evaluación abierta de 1 año para evaluar la seguridad y la eficacia de clorhidrato de guanfacina de liberación prolongada (SPD503) en niños y adolescentes de 6 a 17 años de edad con trastorno por déficit de atención con hiperactividad

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Estudio de fase IIa aleatorizado, doble ciego y controlado con placebo de las vacunas contra el VIH 1 MVA.HTI y ChAdOx1.HTI con el agonista del receptor TLR7 vesatolimod (GS-9620) en la infección por el VIH-1 tratada de forma precoz

  • Protocol code: AELIX-003
  • EudraCT code: 2018-002125-30
  • Pathology: Certes malalties infeccioses i parasitàries
  • Principal investigator:  Curran Fàbregas, Adria
  • Research group:  Malalties infeccioses
  • Service: Infeccioses
  • Phase: Phase II
  • Recruiting: Open
  • Status: Open

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HELIOS-A: Estudio de fase 3, internacional, aleatorizado y abierto para evaluar la eficacia y la seguridad de ALN-TTRSC02 en pacientes conamiloidosis hereditaria por transtiretina (amiloidosis hATTR).

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Efectos del recambio plasmático con albúmina sérica humana al 5% (RP-A 5%) en la supervivencia a corto plazo de sujetos con 'Fallo hepático agudo sobre crónico' (ACLF, por sus siglas en inglés) con alto riesgo de mortalidad hospitalaria

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Ensayo abierto de extensión para evaluar la seguridad a largo plazo de ZX008 (clorhidrato de fenfluramina) en solución oral como tratamiento adyuvante para convulsiones en pacientes con trastornos infrecuentes de convulsiones tales como encefalopatías epilépticas incluidos el síndrome de Dravet y el síndrome de Lennox-Gastaut

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Estudio abierto, multicéntrico y aleatorizado para investigar el tratamiento antirretroviral con inhibidor de la integrasa frente al inhibidor de la proteasa potenciado para pacientes con enfermedad por el VIH avanzada. Estudio Late Presenter Treatment Optimisation (Optimización del tratamiento para pacientes con infección avanzada, LAPTOP).

  • Protocol code: NEAT44
  • EudraCT code: 2018-003481-13
  • Pathology: Certain infectious and parasitic diseases
  • Principal investigator:  Curran Fàbregas, Adria
  • Research group:  Infectious Diseases
  • Service: Infectious
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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A Phase 3, Randomized, Active-Controlled, Double-Blind Clinical Study to Evaluate a Switch to Doravirine/Islatravir (DOR/ISL) Once-Daily in Participants With HIV-1 Virologically Suppressed on Bictegravir/Emtricitabine/Tenofovir Alafenamide(BIC/FTC/TAF)

  • Protocol code: MK-8591A-018
  • EudraCT code: 2019-000587-23
  • Pathology: Certain infectious and parasitic diseases
  • Principal investigator:  Falcó Ferrer, Vicenç
  • Research group:  Infectious Diseases
  • Service: Infectious
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Estudio de fase 3, aleatorizado, doble ciego, controlado con placebo y multicéntrico para evaluar la seguridad y la eficacia de ravulizumab en pacientes adultos sin tratamiento previo con inhibidores del complemento con miastenia gravis generalizada

  • Protocol code: ALXN1210-MG-306
  • EudraCT code: 2018-003243-39
  • Pathology: Malalties del sistema osteomuscular i del teixit connectiu
  • Principal investigator:  Salvadó Figueras, Maria
  • Research group:  Sistema nerviós perifèric
  • Service: Neurology
  • Phase: Phase III
  • Recruiting: Closed
  • Status: Open

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Ensayo clínico aleatorio de fase 3/4 de Andexanet Alfa [Andexanet Alfa inyectable] en hemorragia intracraneal aguda en pacientes que reciben un inhibidor del factor Xa oral

  • Protocol code: 18-513
  • EudraCT code: 2018-002620-17
  • Pathology: Malalties del sistema nerviós
  • Principal investigator:  Molina Cateriano, Carlos
  • Research group:  Stroke research
  • Service: Neurology
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Estudio de fase I, abierto, de grupos paralelos para investigar la seguridad, la tolerabilidad, la eficacia y la farmacocinética de olaparib en pacientes pediátricos con tumores sólidos

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Estudio en fase III, multinacional, doble ciego, aleatorizado y controlado con placebo de MGL-3196 (resmetirom) en pacientes con esteatohepatitis no alcohólica (EHNA) y fibrosis para resolver la EHNA y reducir la progresión a cirrosis y/o a descompensación hepática

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Estudio aleatorizado, doble ciego, controlado con placebo, de gruposparalelos en pacientes con enfermedad de Parkinson con disquinesiamoderada a intensa para evaluar la eficacia y la seguridad y tolerabilidadde dos combinaciones de dosis de JM-010

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Colchicina para la prevención de la fibrilación auricular perioperatoria en pacientes sometidos a cirugía torácica (COP-AF)

  • Protocol code: 2017-001-COPAF
  • EudraCT code: 2017-003836-35
  • Principal investigator:  González Tallada, Anna
  • Service: Anesthesia
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Ensayo en fase III, multicéntrico, aleatorizado, doble ciego y controlado con placebo de olaparib y abiraterona en comparación con placebo y abiraterona como tratamiento de primera línea en varones con cáncer de próstata metastásicoresistente a la castración.

  • Protocol code: D081SC00001
  • EudraCT code: 2018-002011-10
  • Principal investigator:  Valderrama Rodríguez, Angelica
  • Service: Sense classificar
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Estudio en fase 3, aleatorizado, enmascarado para el evaluador y multicéntrico para evaluar la eficiacia y seguridad de ALXN1840 administrado durante 48 semanas en comparación con el tratamiento de referencia en pacientes con enfermedad de Wilson de 12 años de edad o más con un período de extensión de hasta 60 meses

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Ensayo clínico de fase III, multicéntrico, aleatorizado, observador ciego y controlado con placebo para evaluar la recurrencia de herpes zóster y la reactogenicidad, seguridad e inmunogenicidad de la vacuna frente al herpes zóster (HZ/su) de GSK Biologicals cuando se administra por vía intramuscular en una pauta de 0 y 2 meses a adultos de 50 años o más con un episodio previo de herpes zóster

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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.