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Ensayo multicéntrico, aleatorizado, doble ciego y controlado con placebo de 6 meses para evaluar la eficacia, seguridad y la farmacocinética y farmacodinámica de un régimen de finerenona oral ajustado por edad y peso corporal, añadido a un IECA o ARA II, para el tratamiento de pacientes pediátricos, de 6 meses a <18 años, con enfermedad renal crónica y proteinuria

  • Protocol code: 19920
  • EudraCT code: 2021-002071-19
  • Pathology: Malalties del sistema genitourinari
  • Principal investigator:  Ariceta Iraola, Gema
  • Research group:  Fisiopatologia renal
  • Service: Nefrologia Pediàtrica
  • Phase: Fase III
  • Recruiting: Open
  • Status: Iniciat

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Controller: Fundació Hospital Universitari Vall Hebron Institut de Recerca – VHIR- G60594009.
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RINGSIDE: Estudio en fase II//III, aleatorizado y multicéntrico para evaluar AL102 en pacientes con tumores desmoides en progresión

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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 
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ENSAYO CLÍNICO DE FASE III, ALEATORIZADO, DOBLE CIEGO Y CONTROLADO CON PLACEBO PARA EVALUAR LA EFICACIA Y LA SEGURIDAD DEL TRATAMIENTO ADYUVANTE CON ATEZOLIZUMAB O PLACEBO Y TRASTUZUMAB EMTANSINA EN EL CÁNCER DE MAMA CON HER2+ Y ALTO RIESGO DE RECIDIVA DESPUÉS DEL TRATAMIENTO PREOPERATORIO

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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 y controlado con placebo para investigar la eficacia y la seguridad de ligelizumab (QGE031) en el tratamiento de la urticaria crónica inducible (CINDU) en adolescentes y adultos inadecuadamentecontrolados con antihistamínicos H1

  • Protocol code: CQGE031E12301
  • EudraCT code: 2020-003018-11
  • Pathology: Malalties de la pell i del teixit subcutani
  • Principal investigator:  Labrador Horrillo, Moisés
  • Research group:  Malalties sistèmiques
  • Service: Medicina Interna
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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POETYK PsA-2 (055) - Estudio fase 3, multicéntrico, aleatorizado, doble ciego y controlado con placebo para evaluar la eficacia y la seguridad del deucravacitinib en pacientes con artritis psoriásica activa (APs) naïve a medicamentos biológicos antirreumáticos modificadores de la enfermedad o que previamente han sido tratados con un inhibidor del TNFa

  • Protocol code: IM011-055
  • EudraCT code: 2020-005099-36
  • Pathology: Símptomes, signes i troballes anormals clíniques i de laboratori, no classificades enlloc més
  • Principal investigator:  Marsal Barril, Sara
  • Research group:  Reumatologia
  • Service: Reumatologia
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Ensayo multicéntrico Fase III, aleatorizado, doble-ciego, controlado frente a placebo, para evaluar la eficacia de ciclosilicato de sodio y zirconio en la progresión de la enfermedad renal crónica (ERC) en pacientes con ERC e hiperpotasemia o con riesgo de hiperpotasemia

  • Protocol code: D9488C00001
  • EudraCT code: 2021-001911-96
  • Pathology: Symptoms, signs, and abnormal clinical and laboratory findings, not elsewhere classified
  • Principal investigator:  Soler Romeo, Maria Jose
  • Research group:  Nefrologia i trasplantament renal
  • Service: Nefrologia
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Ensayo aleatorizado, doble ciego (dentro de los grupos de dosis), controlado con placebo y con grupos paralelos para investigar los efectos de diferentes dosis de BI 685509 administradas por vía oral durante 20 semanas sobre la reducción del UACR en pacientes con nefropatía no diabética.

  • Protocol code: 1366-0022
  • EudraCT code: 2020-002930-33
  • 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: Fase II
  • Recruiting: Open
  • Status: Open

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Estudio de fase III, multicéntrico, aleatorizado, doble ciego, controlado con placebo, para evaluar la seguridad y eficacia a largo plazo de lanifibranor en pacientes adultos con esteatohepatitis no alcohólica (EHNA) sin cirrosis y estadio de fibrosis hepática grado 2 (F2)/grado 3 (F3)

  • Protocol code: 337HNAS20011
  • EudraCT code: 2020-004986-38
  • Pathology: Malalties del sistema digestiu
  • Principal investigator:  Pericàs Pulido, Juan Manuel
  • Research group:  Malalties hepàtiques
  • Service: Hepatologia
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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DTG // 3TC frente a BIC // FTC // TAF como terapia de mantenimiento en personas que viven con VIH: ensayo clínico abierto y aleatorizado

  • Protocol code: GESIDA11720
  • EudraCT code: 2020-003686-18
  • Pathology: Certes malalties infeccioses i parasitàries
  • Principal investigator:  Curran Fàbregas, Adria
  • Research group:  Malalties infeccioses
  • Service: Infeccioses
  • Phase: Fase IV
  • Recruiting: Open
  • Status: Open

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Ensayo multicéntrico, aleatorizado, de grupos paralelos, controlado con placebo (doble ciego) y con tratamiento activo (abierto) para comparar la eficacia y seguridad de lonapegsomatropina una vez a la semana frente a placebo una vez a la semana y un producto de somatropina diaria en adultos con deficiencia de hormona del crecimiento

  • Protocol code: TCH-306
  • EudraCT code: 2020-000929-42
  • Pathology: Symptoms, signs, and abnormal clinical and laboratory findings, not elsewhere classified
  • Principal investigator:  Biagetti Biagetti, Betina
  • Research group:  Diabetis i metabolisme
  • Service: Endocrinologia
  • Phase: Phase II
  • 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 adolescentes de entre 12 y 17 años con migraña crónica - Estudio REBUILD-2

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Estudio en fase III, multicéntrico, doble ciego y aleatorizado para evaluar la eficacia y seguridad de OPT-302 intravítreo en combinación con aflibercept, en comparación con aflibercept en monoterapia, en participantes con degeneración macular asociada a la edad (DMAE)

  • Protocol code: OPT-302-1005
  • EudraCT code: 2020-004694-46
  • Pathology: Malalties de l’ull i dels seus annexos
  • Principal investigator:  García Arumí, José
  • Research group:  Oftalmologia
  • Service: Oftalmologia
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Estudio de fase 2b, aleatorizado, doble ciego y controlado con placebo para evaluar la eficacia y la seguridad de MK-3655 en personas con esteatohepatitis no alcohólica precirrótica.

  • Protocol code: MK-3655-001
  • EudraCT code: 2019-003048-63
  • Pathology: Digestive system diseases
  • Principal investigator:  Vargas Blasco, Victor Manuel
  • Research group:  Liver Diseases
  • Service: Hepatology
  • Phase: Phase II
  • Recruiting: Open
  • Status: Open

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Evaluación de la eficacia y seguridad de la inmunoterapia subcutánea(Beltavac®) con extracto alergénico polimerizado de mezcla de ácaros del mpolvo en pacientes con rinitis//rinoconjuntivitis alérgica

  • Protocol code: PRO-RCT-ACAROS-2018-01
  • EudraCT code: 2018-003427-11
  • Pathology: Symptoms, signs, and abnormal clinical and laboratory findings, not elsewhere classified
  • Principal investigator:  Cardona Dahl, Victòria
  • Research group:  Systemic Diseases
  • Service: Internal Medicine
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Estudio multicéntrico, aleatorizado, doble ciego, de grupos paralelos y controlado con placebo para evaluar la eficacia y la seguridad de iptacopán (LNP023) en la glomerulopatía C3.

  • Protocol code: CLNP023B12301
  • EudraCT code: 2020-004589-21
  • 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 III
  • Recruiting: Open
  • Status: Open

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Estudio de seguimiento, abierto, a largo plazo, para evaluar los efectos de sotatercept añadido a la terapia de base de la hipertensión arterial pulmonar (HAP) para el tratamiento de la HAP

  • Protocol code: A011-12
  • EudraCT code: 2020-005061-13
  • Pathology: Malalties del sistema respiratori
  • Principal investigator:  Berastegui Garcia, Cristina
  • Research group:  Pneumologia
  • Service: Pneumologia
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Estudio fase 2//3, aleatorizado, doble ciego y controlado con placebo, de BLU-263 en la mastocitosis sistémica indolente

  • Protocol code: BLU-263-1201
  • EudraCT code: 2020-005173-28
  • Pathology: Malalties de la sang i dels òrgans hematopoètics i certs trastorns que afecten el mecanisme de la immunitat
  • Principal investigator:  Guilarte Clavero, Mar
  • Research group:  Systemic Diseases
  • Service: Internal Medicine
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Estudio clínico aleatorizado, doble ciego, controlado con placebo, multicéntrico,ininterrumpido, adaptativo, de seguridad y búsqueda de dosis en fase III de la transferencia génicamediada por VAA con UX701 para el tratamiento de la enfermedad de Wilson.

  • Protocol code: UX701-CL301
  • EudraCT code: 2020-005266-34
  • Pathology: Digestive system diseases
  • Principal investigator:  Quintero Bernabeu, Jesús
  • Research group:  Cirurgia general
  • Service: Pediatria General i Especialitats
  • Phase: Fase I
  • 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.
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 doble ciego, aleatorizado, controlado con placebo y extensión abierta a largo plazo para evaluar la eficacia y la seguridad de elafibranor 80 mg en pacientes con colangitis biliar primaria con respuesta insuficiente o intolerancia al ácido ursodesoxicólico

  • Protocol code: GFT505B-319-1
  • EudraCT code: 2019-004941-34
  • Pathology: Digestive system diseases
  • Principal investigator:  Villagrasa Vilella, Ares Aurora
  • Research group:  Liver Diseases
  • Service: Hepatology
  • 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.
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 sin enmascaramiento para evaluar la seguridad y la eficacia a largoplazo de CSL312 (Garadacimab) en el tratamiento profiláctico del angioedema hereditario

  • Protocol code: CSL312_3002
  • EudraCT code: 2020-003918-12
  • Pathology: Malalties del sistema nerviós
  • Principal investigator:  Guilarte Clavero, Mar
  • Research group:  Systemic Diseases
  • Service: Internal Medicine
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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.