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Ensayo clínico de viabilidad de la combinación de AloCelyvir con quimioterapia y radioterapia para el tratamiento de niños y adolescentes con tumores sólidos extra-craneales en recaída o refractarios.

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Controller: Fundació Hospital Universitari Vall Hebron Institut de Recerca – VHIR- G60594009.
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Estudio de fase 3 multicéntrico, doble ciego, aleatorizado, controlado con placebo y de grupos paralelos para evaluar la eficacia, seguridad y farmacocinética de apremilast en niños de 5 a menos de 18 años de edad con artritis psoriásica juvenil activa (PEAPOD, por sus siglas in inglés)

  • Protocol code: 20190529
  • EudraCT code: 2019-002788-88
  • Pathology: Símptomes, signes i troballes anormals clíniques i de laboratori, no classificades enlloc més
  • Principal investigator:  Moreno Ruzafa, Estefania
  • Research group:  Reumatologia
  • Service: Reumatologia
  • Phase: Fase III
  • Recruiting: Closed
  • 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 
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Estudio de extensión abierto, de fase 3, multicéntrico, de zilucoplan en pacientes con miastenia gravis generalizada

  • Protocol code: RA101495-02.302 (MG0011)
  • EudraCT code: 2019-001565-33
  • Pathology: Malalties del sistema osteomuscular i del teixit connectiu
  • Principal investigator:  Juntas Morales, Raul
  • Research group:  Sistema nerviós perifèric
  • Service: Neurologia
  • Phase: Phase III
  • Recruiting: Open
  • Status: Tancat

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Controller: Fundació Hospital Universitari Vall Hebron Institut de Recerca – VHIR- G60594009.
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Estudio de seguridad posautorización para evaluar la seguridad y la eficacia a largo plazo de la administración repetida de darvadstrocel en pacientes con enfermedad de Crohn y fístulas perianales complejas (ASPIRE)

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Estudio aleatorizado, multicéntrico y multinacional, con doble enmascaramiento y controlado con placebo, con grupos paralelos, de dosis única y diseño adaptativo para evaluar la eficacia y seguridad del glenzocimab utilizado como tratamiento complementario al tratamiento habitual en las 4,5 horas siguientes a un ictus isquémico agudo.

  • Protocol code: ACT-CS-005
  • EudraCT code: 2021-002148-56
  • Pathology: Malalties del sistema circulatori
  • Principal investigator:  Molina Cateriano, Carlos
  • Research group:  Recerca en ictus
  • Service: Neurology
  • Phase: Phase III
  • Recruiting: Open
  • Status: Close

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Controller: Fundació Hospital Universitari Vall Hebron Institut de Recerca – VHIR- G60594009.
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Ensayo aleatorizado, doble ciego, controlado con placebo, de dosis repetidas y multicéntrico, para evaluar la eficacia, seguridad, tolerabilidad y farmacocinética de HZN-825 en pacientes con esclerosis sistémica cutánea difusa

  • Protocol code: HZNP-HZN-825-301
  • EudraCT code: 2020-005764-62
  • Pathology: Symptoms, signs, and abnormal clinical and laboratory findings, not elsewhere classified
  • Principal investigator:  Guillen Del Castillo, Alfredo
  • Research group:  Malalties sistèmiques
  • Service: Medicina Interna
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Estudio en fase II abierto para evaluar la seguridad y eficacia de DCR-PHXC en pacientes con Hiperoxaluria primaria tipo 1 o 2 e insuficiencia renal grave con o sin diálisis

  • Protocol code: DCR-PHXC-204
  • EudraCT code: 2020-002826-97
  • Pathology: Malalties del sistema genitourinari
  • Principal investigator:  Ariceta Iraola, Gema
  • Research group:  Fisiopatologia renal
  • Service: Nefrologia Pediàtrica
  • Phase: Fase II
  • Recruiting: Open
  • Status: Open

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Legitimation: Your consent. The data requested is necessary and your request cannot be processed if you do not provide them.
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Estudio multicéntrico, aleatorizado, doble ciego, controlado con placebo y de grupos paralelos para evaluar la eficacia, la seguridad y la tolerabilidad de soticlestat como tratamiento adyuvante en sujetos pediátricos y en adultos jóvenes con síndrome de Dravet (SD)

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udio Fase 3 Abierto de Neoadyuvancia con Trastuzumab Deruxtecan (TDXd) en monoterapia o T-DXd seguido de THP comparado con ddAC-THP enpacientes con cáncer de mama en estadio temprano HER2-positivo de alto riesgo (DESTINY-Breast 11)

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Estudio en fase II, abierto, aleatorizado y de múltiples cohortes para evaluar la eficacia, la seguridad y la farmacocinética preliminares de BIVV020 para la prevención y el tratamiento del rechazo mediado por anticuerpos en adultos receptores de trasplante renal.

  • Protocol code: ACT17012
  • EudraCT code: 2021-000010-41
  • Pathology: Symptoms, signs, and abnormal clinical and laboratory findings, not elsewhere classified
  • Principal investigator:  Bestard Matamoros, Oriol
  • Research group:  Nefrologia i trasplantament renal
  • Service: Nefrologia
  • Phase: Phase II
  • Recruiting: Open
  • Status: Open

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Ensayo clínico de fase II con dos cohortes paralelas en pacientes con receptores de estrógenos negativos o enfermedad no-luminal según PAM50, Tratamiento con atezolizumab en combinación con trastuzumab y vinorelbina en el cáncer de mama avanzado/metastásico HER2-positivo – Estudio ATREZZO

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ESTUDIO DE FASE III ALEATORIZADO, MULTICÉNTRICO, DOBLE CIEGO Y CONTROLADO CON PLACEBO PARA EVALUAR LA EFICACIA Y LA SEGURIDAD DE TRASTUZUMAB EMTANSINA EN COMBINACIÓN CON ATEZOLIZUMAB O PLACEBO EN PACIENTES CON CÁNCER DE MAMA LOCALMENTE AVANZADO O METASTÁSICO POSITIVO PARA HER2 Y PD-L1 QUE HAYAN RECIBIDO PREVIAMENTE TRATAMIENTO BASADO EN TRASTUZUMAB (+/- PERTUZUMAB) Y TAXANOS (KATE 3).

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Estudio de extensión abierto para evaluar rozanolixizumab en pacientes con miastenia gravis generalizada

  • Protocol code: MG0007
  • EudraCT code: 2020-003230-20
  • Pathology: Nervous system diseases
  • Principal investigator:  Juntas Morales, Raul
  • Research group:  Peripheral Nervous System
  • Service: Neurology
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Estudio fase 2, aleatorizado, doble ciego, controlado con placebo, de grupos paralelos y de múltiples dosis, para evaluar la eficacia y la seguridad de BMS-986263 en adultos con cirrosis compensada por esteatohepatitis no alcohólica(EHNA)

  • Protocol code: IM025-017
  • EudraCT code: 2019-003932-22
  • Pathology: Symptoms, signs, and abnormal clinical and laboratory findings, not elsewhere classified
  • Principal investigator:  Pericàs Pulido, Juan Manuel
  • Research group:  Malalties hepàtiques
  • Service: Hepatologia
  • Phase: Phase II
  • Recruiting: Open
  • Status: Open

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Implantación de células derivadas del músculo esquelético para el tratamiento de la incontinencia fecal: estudio de fase III, aleatorizado, controlado, doble ciego y dos brazos de tratamiento.

  • Protocol code: IC-01-02-5-009
  • EudraCT code: 2021-001376-42
  • Pathology: Digestive system diseases
  • Principal investigator:  Espín Basany, Eloy
  • Research group:  Cirurgia general
  • Service: Cirurgia General
  • Phase: Phase III
  • Recruiting: Closed
  • Status: Close

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Estudio multicéntrico, aleatorizado, controlado, abierto y ciego para el evaluador para evaluar la eficacia, la seguridad, la farmacocinética y la farmacodinámica de ALXN1840 en comparación con el tratamiento habitualen participantes pediátricos con enfermedad de Wilson

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Efecto de la semaglutida en sujetos con esteatohepatitis no alcohólica ni cirrótica

  • Protocol code: NN9931-4553
  • EudraCT code: 2019-004594-44
  • Pathology: Symptoms, signs, and abnormal clinical and laboratory findings, not elsewhere classified
  • Principal investigator:  Pericàs Pulido, Juan Manuel
  • Research group:  Liver Diseases
  • Service: Sense classificar
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Estudio abierto en fase IIIb para evaluar la seguridad de un tratamiento combinado con elexacaftor/tezacaftor/ivacaftor en sujetos con fibrosis quística

  • Protocol code: VX20-445-121
  • EudraCT code: 2020-004885-21
  • Pathology: Malalties del sistema respiratori
  • Principal investigator:  GARTNER TIZZANO, SILVIA
  • Research group:  Creixement i desenvolupament
  • Service: Obstetrícia
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Estudio aleatorizado, con enmascaramiento doble y comparativo con un placebo,en el que se evalúa galcanezumab en pacientes de entre 6 y 17 años con migrañaepisódica - Estudio REBUILD-1

  • Protocol code: I5Q-MC-CGAS
  • EudraCT code: 2017-004351-23
  • Pathology: Nervous system diseases
  • Principal investigator:  Pozo Rosich, Patricia
  • Research group:  Cefalea i dolor neurològic
  • Service: Neurology
  • 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 multicéntrico, aleatorizado, doble ciego, controlado con placebo de 52 semanas de duración para evaluar la eficacia clínica y la seguridad de ligelizumab (QGE031) en la disminución de la sensibilidad a los cacahuetes en pacientes conalergia al cacahuete.

  • Protocol code: CQGE031G12301
  • EudraCT code: 2020-005339-56
  • Pathology: Symptoms, signs, and abnormal clinical and laboratory findings, not elsewhere classified
  • Principal investigator:  Labrador Horrillo, Moisés
  • Research group:  Systemic Diseases
  • Service: Internal Medicine
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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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.