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Estudio de Extensión En Régimen Abierto (ERA) para evaluar la eficacia y laseguridad del tratamiento con Nefecon en pacientes con Nefropatía por IgAque han finalizado el estudio Nef-301

  • Protocol code: Nef-301 OLE
  • EudraCT code: 2020-003308-14
  • Pathology: Símptomes, signes i troballes anormals clíniques i de laboratori, no classificades enlloc més
  • Principal investigator:  Agraz Pamplona, Irene
  • Research group:  Nefrologia i trasplantament renal
  • Service: Nefrologia
  • Phase: Fase III
  • Recruiting: Closed
  • Status: Iniciat

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Estudio abierto de fase III para evaluar la eficacia y la seguridad de Replagal® en sujetos con enfermedad de Fabry que no han recibido tratamiento previo

  • Protocol code: SHP675-301
  • EudraCT code: 2018-004689-32
  • Pathology: Malalties del sistema nerviós
  • Principal investigator:  Camprodon Gomez, Maria
  • Research group:  Malalties neurodegeneratives
  • Service: Medicina Interna
  • Phase: Phase III
  • Recruiting: Closed
  • Status: Open

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Un estudio para evaluar la eficacia y seguridad del PRM-151 en pacientes con fibrosis pulmonar idiopática

  • Protocol code: WA42293
  • EudraCT code: 2020-000791-38
  • Pathology: Malalties del sistema respiratori
  • Principal investigator:  Villar Gomez, Ana
  • Research group:  Pneumologia
  • Service: Pneumologia
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Antibióticos alternativos orales y?neuropenetrantes?para pacientes con sífilis

  • Protocol code: Trep-AB
  • EudraCT code: 2020-005604-19
  • Pathology: Certes malalties infeccioses i parasitàries
  • Principal investigator:  Arando Lasagabaster, Maider
  • Research group:  Malalties infeccioses
  • Service: Infeccioses
  • Phase: Phase III
  • Recruiting: Closed
  • Status: Open

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Estudio de fase 1b de aumento de la dosis de abemaciclib en combinación con temozolomida e irinotecán (parte A) y de abemaciclib en combinación con temozolomida (parte b) en niños y adultos jóvenes con tumores sólidos recidivantes/resistentes al tratamiento.A Phase 1b Dose Escalation Study of Abemaciclib in Combination with Temozolomide and Irinotecan (Part A) and Abemaciclib in Combination with Temozolomide (Part B) in Pediatric and Young Adult Patients with Relapsed/Refractory Solid Tumors

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Estudio de fase 3, aleatorizado, doble ciego y controlado con placebo para evaluar la eficacia, la seguridad y la tolerabilidad de Brensocatib administrado una vez al día durante 52 semanas en sujetos con bronquiectasias sin fibrosis quística: estudio ASPEN

  • Protocol code: INS1007-301
  • EudraCT code: 2020-003688-25
  • Pathology: Diseases of the respiratory system
  • Principal investigator:  Polverino , Eva
  • Research group:  Pneumology
  • Service: Pneumology
  • Phase: Phase III
  • Recruiting: Open
  • Status: Tancat

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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 fase 3, aleatorizado, doble ciego, controlado con placebo, de grupos paralelos para evaluar la eficacia y seguridad de tolebrutinib (SAR442168) en adultos con miastenia gravis generalizada (MGg)

  • Protocol code: EFC17262
  • EudraCT code: 2021-003898-59
  • Pathology: Nervous system diseases
  • Principal investigator:  Juntas Morales, Raul
  • Research group:  Sistema nerviós perifèric
  • Service: Neurologia
  • Phase: Phase III
  • Recruiting: Closed
  • Status: Open

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Ensayo Clínico fase III, multicéntrico, abierto y aleatorizado para evaluar la eficacia del tratamiento con Ciclosilicato de Sodio y Zirconio (Lokelma), comparado con la terapia estándar, para el manejo de la hiperpotasemia en pacientes conenfermedad renal crónica (ERC) e historial de insuficiencia cardiaca

  • Protocol code: KEEP ON (ESR-19-20217)
  • EudraCT code: 2020-003229-47
  • Pathology: Symptoms, signs, and abnormal clinical and laboratory findings, not elsewhere classified
  • Principal investigator:  Soler Romeo, Maria Jose
  • Research group:  Nephrology and kidney transplantation
  • Service: Nephrology
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Estudio en fase III multicéntrico, aleatorizado, doble ciego y controlado con placebo para la evaluación de la eficacia y seguridad de anifrolumab subcutáneo en pacientes adultos con lupus eritematoso sistémico

  • Protocol code: D3465C00001
  • EudraCT code: 2020-004529-22
  • Pathology: Symptoms, signs, and abnormal clinical and laboratory findings, not elsewhere classified
  • Principal investigator:  Cortes Hernandez, Josefina
  • Research group:  Reumatologia
  • Service: Reumatologia
  • 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 
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Ensayo Clínico de transferencia génica fase I/II con scAAV9.U1a.hSGSH para la Mucopolisacaridosis (MPS) tipo IIIA

  • Protocol code: ABT-001
  • EudraCT code: 2015-003904-21
  • Pathology: Symptoms, signs, and abnormal clinical and laboratory findings, not elsewhere classified
  • Principal investigator:  Del Toro Riera, Mireia
  • Research group:  Neurologia pediàtrica
  • Service: Pediatria General i Especialitats
  • Phase: Fase II
  • Recruiting: Open
  • Status: Open

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Estudio de fase II, doble ciego, aleatorizado y controlado con placebo para evaluar la eficacia y la seguridad de ravulizumab en participantes adultos con nefritis lúpica (NL) proliferativa o nefropatía por inmunoglobulina A (NIgA)

  • Protocol code: ALXN1210-NEPH-202
  • EudraCT code: 2020-001537-13
  • Pathology: Symptoms, signs, and abnormal clinical and laboratory findings, not elsewhere classified
  • Principal investigator:  Agraz Pamplona, Irene
  • Research group:  Nephrology and kidney transplantation
  • Service: Nephrology
  • Phase: Phase II
  • Recruiting: Open
  • Status: Open

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ESTUDIO CLINICO DE DETERMINACION DE TIEMPOS Y DESPLAZAMIENTOS DE LA COMBINACION DE UNA DOSIS FIJA SUBCUTÁNEA DE PERTUZUMAB Y TRASTUZUMAB PARA EL TRATAMIENTO DE PACIENTES CON CÁNCER DE MAMA PRECOZ HER2 POSITIVO

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Ensayo en fase III, aleatorizado, con enmascaramiento doble, comparativo con placebo y multicéntrico para evaluar la eficacia y la seguridad de Diamyd® en la conservación del funcionamiento de las células ß endógenasen adolescentes y adultos con un diagnóstico reciente de diabetes de tipo 1que presentan el haplotipo genético HLA DR3-DQ2

  • Protocol code: DIAGNODE-3 (D/P3/21/7)
  • EudraCT code: 2021-002731-32
  • Pathology: Malalties endocrines, nutricionals i metabòliques
  • Principal investigator:  Hernández Pascual, Cristina
  • Research group:  Diabetis i metabolisme
  • Service: Endocrinologia
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Estudio de búsqueda de dosis de fase 2b para evaluar la eficacia y seguridad de rozibafusp alfa (AMG 570) en sujetos con lupus eritematoso sistémico (LES) activo con respuesta inadecuada al tratamiento estándar (SOC)

  • Protocol code: 20170588
  • EudraCT code: 2019-000328-16
  • Pathology: Symptoms, signs, and abnormal clinical and laboratory findings, not elsewhere classified
  • Principal investigator:  Cortes Hernandez, Josefina
  • Research group:  Rheumatology
  • Service: Rheumatology
  • Phase: Phase II
  • Recruiting: Open
  • Status: Open

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Ensayo clínico de prueba de concepto (PoC) ANRS HB07 IP-cure-B. Educar el entorno inmunológico del hígado a través de la estimulación de TLR8 seguida de la interrupción de NUC

  • Protocol code: ANRSHB07
  • EudraCT code: 2020-004376-18
  • Pathology: Symptoms, signs, and abnormal clinical and laboratory findings, not elsewhere classified
  • Principal investigator:  Buti Ferret, Maria
  • Research group:  Malalties hepàtiques
  • Service: Hepatologia
  • Phase: Phase II
  • Recruiting: Open
  • Status: Open

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Estudio de continuación abierto para evaluar la seguridad y eficacia a largo plazo de la solución inyectable DCR-PHXC (uso subcutáneo) en pacientes con hiperoxaluria primaria.

  • Protocol code: DCR-PHXC-301
  • EudraCT code: 2018-003099-10
  • Pathology: Symptoms, signs, and abnormal clinical and laboratory findings, not elsewhere classified
  • Principal investigator:  Ariceta Iraola, Gema
  • Research group:  Fisiopatologia renal
  • Service: Nefrologia Pediàtrica
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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IOCYTE AMI-3 Estudio de fase 3, multicéntrico, aleatorizado, doble ciego ycontrolado con placebo de FDY-5301 intravenoso en pacientes con infarto de miocardio con elevación del segmento ST anterior

  • Protocol code: FDY-5301-302
  • EudraCT code: 2021-001924-16
  • Pathology: Symptoms, signs, and abnormal clinical and laboratory findings, not elsewhere classified
  • Principal investigator:  García del Blanco, Bruno
  • Research group:  Malalties cardiovasculars
  • Service: Cardiologia
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Estudio fase 1b, abierto, de un solo brazo de tratamiento con Epcoritamab en pacientes pediátricos con neoplasias de células B maduras recidivantes/refractarias.

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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 CLINICO DE DETERMINACION DE TIEMPOS Y DESPLAZAMIENTOS DE LA COMBINACION DE UNA DOSIS FIJA SUBCUTÁNEA DE PERTUZUMAB Y TRASTUZUMAB PARA EL TRATAMIENTO DE PACIENTES CON CÁNCER DE MAMA PRECOZ HER2 POSITIVO

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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.
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.

Estrategia sin quimioterapia basada en la repuesta patológica completa con pertuzumab-trastuzumab por vía subcutánea y T-DM1 en cáncer de mama HER2 positivo en estadio inicial (PHERGain-2)

Contact Form

I have read and accept the data protection policy *.
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.