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Estudio internacional, de fase 2b, aleatorizado ydoble ciego para investigar la eficacia y la seguridad de redasemtide (S-005151) comparado con placebo enpacientes mayores de edad con ictus isquémico agudo que no son candidatos a tratamiento con activadortisular del plasminógeno o trombectomía

  • Protocol code: 2138P2231
  • EudraCT code: No aplica
  • Pathology: Malalties del sistema circulatori
  • Principal investigator:  Molina Cateriano, Carlos
  • Research group:  Recerca en ictus
  • Service: Neurologia
  • Phase: Fase II
  • Recruiting: Closed
  • Status: Iniciat

Contact Form

I have read and accept the data protection policy *.

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 aleatorizado, doble ciego, controlado con placebo, de grupos paralelos que evalúa los efectos del fármaco oral BI685509 (ajuste de dosis a un régimen de dosis fija) en hipertensión portal después de 8 semanas de tratamiento en pacientes con hipertensión clínicamente significativa (CSPH) en cirrosis descompensada después de su primer evento de descompensación, estabilizados CTP 5-7.

  • Protocol code: 1366-0055
  • EudraCT code: No aplica
  • Pathology: Símptomes, signes i troballes anormals clíniques i de laboratori, no classificades enlloc més
  • Principal investigator:  Pericàs Pulido, Juan Manuel
  • Research group:  Malalties hepàtiques
  • Service: Sense classificar
  • Phase: Phase II
  • Recruiting: Closed
  • Status: Open

Contact Form

I have read and accept the data protection policy *.

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 EN FASE III, ALEATORIZADO, DOBLE CIEGO Y CONTROLADO CON PLACEBO PARA EVALUAR LA SEGURIDAD Y LA EFICACIA DE EFRUXIFERMIN EN SUJETOS CON ESTEATOHEPATITIS NO ALCOHÓLICA (EHNA) NO CIRRÓTICA Y FIBROSIS

  • Protocol code: AK-US-001-0105
  • EudraCT code: No aplica
  • Pathology: Tumors
  • Principal investigator:  Pericàs Pulido, Juan Manuel
  • Research group:  Liver Diseases
  • Service: Hepatologia
  • Phase: Fase III
  • Recruiting: Open
  • Status: Open

Contact Form

I have read and accept the data protection policy *.

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.

A SINGLE-ARM, OPEN-LABEL, MULTI-CENTRE, PHASE IB STUDY EVALUATING THE SAFETY AND PRELIMINARY EFFICACY OF AUTO1 IN PAEDIATRIC PATIENTS WITH CD19-POSITIVE RELAPSED/ REFRACTORY (R/R) B-CELL ACUTE LYMPHOBLASTIC LEUKEMIA (B ALL) AND AGGRESSIVE MATURE B-CELL NON-HODGKIN LYMPHOMA (B NHL)

Contact Form

I have read and accept the data protection policy *.

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 fase 2/3, aleatorizado, doble ciego, controlado con placebo, de grupos paralelos para evaluar la eficacia y la seguridad de belimumab ..administrado por vía subcutánea en adultos con enfermedad pulmonar intersticial asociada a esclerosis sistémica (SSc-ILD).

Contact Form

I have read and accept the data protection policy *.

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.

A Phase 3, randomised, double-blind, parallel-group, event driven, cardiovascular safety study with BI 456906 administered subcutaneously compared with placebo in participants with overweight or obesity with established cardiovascular disease (CVD) or chronic kidney disease, and/or at least two weight related complications or risk factors for CVD

  • Protocol code: 1404-0040
  • EudraCT code: No aplica
  • Pathology: Malalties endocrines, nutricionals i metabòliques
  • Principal investigator:  Simó Canonge, Rafael
  • Research group:  Diabetis i metabolisme
  • Service: Endocrinologia
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

Contact Form

I have read and accept the data protection policy *.

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.

Ensayo Fase III aleatorizado, doble ciego, de grupos paralelos, controlado con placebo para evaluar la eficacia y seguridad de Tezepelumab en pacientes con Esofagitis Eosinofílica

  • Protocol code: D5244C00001
  • EudraCT code: 2022-001294-31
  • Pathology: Symptoms, signs, and abnormal clinical and laboratory findings, not elsewhere classified
  • Principal investigator:  Guilarte Clavero, Mar
  • Research group:  Systemic Diseases
  • Service: Internal Medicine
  • Phase: Phase III
  • Recruiting: Closed
  • Status: Open

Contact Form

I have read and accept the data protection policy *.

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.

A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Oral Inhalation of Seralutinib for the Treatment of Pulmonary Arterial Hypertension (PAH)

  • Protocol code: GB002-3101
  • EudraCT code: No aplica
  • Pathology: Diseases of the respiratory system
  • Principal investigator:  López Meseguer, Manuel
  • Research group:  Pneumologia
  • Service: Pneumologia
  • Phase: Phase III
  • Recruiting: Closed
  • Status: Open

Contact Form

I have read and accept the data protection policy *.

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.

“ENSAYO EUROPEO DE PRUEBA DE CONCEPTO BASADO EN LA ESTRATIFICACIÓN TERAPÉUTICA SEGÚN LAS ANOMALÍAS MOLECULARES EN TUMORES EN RECAÍDA O REFRACTARIOS”. “EUROPEAN PROOF-OF-CONCEPT THERAPEUTIC STRATIFICATION TRIAL OF MOLECULAR ANOMALIES IN RELAPSED OR REFRACTORY TUMORS

Contact Form

I have read and accept the data protection policy *.

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.

A Phase 2, Multicenter, Randomized, Double-Blinded, Placebo-Controlled Study to Assess the Safety, Efficacy, and Tolerability of ARGX-117 in Improving Allograft Function in Recipients of a Deceased Donor Renal Allograft at Risk for Delayed Graft Function

Contact Form

I have read and accept the data protection policy *.

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.
Year
2024
Títol Complet
Servei de gestió integral d'administració de personal i aspectes associats, portal de l'empleat/da i registre horari per la Fundació Hospital Universitari Vall Hebron - Institut de Recerca (VHIR).
Expedient
SERVEIS DE GESTIÓ ADMINISTRACIÓ DE PERSONAL
Codi
24967298
Data publicació
Year
2024
Títol Complet
Serveis d’auditoria interna per evidenciar el nivell de compliment dels requisits del Sistema de Gestió de la Qualitat ISO 9001:2015, a càrrec de la Unitat de Qualitat de la Fundació Hospital Universitari Vall d’Hebron - Institut de Recerca (VHIR).
Expedient
AUDITORIA INTERNA
Codi
24967297
Data publicació
Year
2024
Títol Complet
Development of a software for the management of candidatures an personnel selection, for the Human Resources Area of the Fundació Hospital Universitari Vall Hebron - Institut de Recerca (VHIR).
Expedient
RECRUITMENT SOFTWARE
Codi
24967217
Data publicació
Year
2024
Títol Complet
Servicios de genotipado mediante Array GSAv4, destinado al Grupo de Psiquiatría, Salud Mental y Adicciones de la Fundació Hospital Universitari Vall Hebron – Institut de Recerca (VHIR).
Expedient
GENOTIPADO MEDIANTE ARRAY GSA (202228-30)
Codi
24967064
Data publicació
Year
2024
Títol Complet
Contratación del servicio de secuenciación avanzada (con y sin análisis bioinformático) mediante las siguientes técnicas genómicas: Whole Genome Sequencing (WGS) y RNA sequencing (RNAseq) destinado al Grupo de Genética Del Cáncer Hereditario de la de la Fundació Hospital Universitari Vall Hebron - Institut de Recerca (VHIR), a cargo del proyecto PI22/01200 titulado “Secuenciación del genoma completo como primera prueba para mejorar el diagnóstico genético del cáncer de mama/ovario hereditario” subvencionado por el Instituto de Salud Carlos III (ISCIII) y cofinanciado por la Unión Europea.
Expedient
SECUENCIACIÓN DEL GENOMA (PI22/01200)
Codi
24966638
Data publicació
Year
2024
Data d'inici
Data de tancament
Grup de recerca
Descripció
Postdoc scientist - Advanced Chronic Liver Disease Laboratory_20240093
Codi
2024-93
Reclutant
Inactiu
Year
2024
Data d'inici
Data de tancament
Grup de recerca
Descripció
PhD candidate - Chronic Liver Disease Group -Liver Unit_
Codi
2024-94
Reclutant
Inactiu
Year
2024
Data d'inici
Data de tancament
Descripció
Psychiatrist Researcher-Psychiatry, Mental Health and Addictions Research Group_20240090
Codi
2024-90
Reclutant
Inactiu
Year
2024
Data d'inici
Data de tancament
Descripció
Nurse Psychiatrist-Mental Health and Addictions Group_20240091
Codi
2024-91
Reclutant
Inactiu