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Year
2025
Referencia
J Control Release. 2025 Mar 10:113616. doi: 10.1016/j.jconrel.2025.113616.
Tipus publicació
Paper in international publication
DOI
http://dx.doi.org/10.1016/j.jconrel.2025.113616
Revista
JOURNAL OF CONTROLLED RELEASE
Títol Complet
Preclinical evaluation of several polymeric micelles identifies Soluplus(R)-docetaxel as the most effective candidate in multiple glioblastoma models.
Codi
75255
PMID
https://pubmed.ncbi.nlm.nih.gov/40073942
Nom Autors
Abasolo, Ibane; Alcina, Angels; Andrade, Fernanda; Campos-Moreno, Sofia; Costa, Roser Ferrer; Diaz-Riascos, Zamira V; Fischer-Albiol, Narine; Garcia, Belen; German-Cortes, Julia; Herrero, Raquel et al.
DOI número
10.1016/j.jconrel.2025.113616
Year
2025
Referencia
Med Image Anal. 2025 Mar 7;102:103531. doi: 10.1016/j.media.2025.103531.
Tipus publicació
Paper in international publication
DOI
http://dx.doi.org/10.1016/j.media.2025.103531
Revista
MEDICAL IMAGE ANALYSIS
Títol Complet
SpinFlowSim: A blood flow simulation framework for histology-informed diffusion MRI microvasculature mapping in cancer.
Codi
75256
PMID
https://pubmed.ncbi.nlm.nih.gov/40073583
Nom Autors
Bernatowicz, Kinga; Escobar, Manuel; Fieremans, Els; Garralda, Elena; Grigoriou, Athanasios; Grussu, Francesco; Novikov, Dmitry S; Nuciforo, Paolo; Palombo, Marco; Perez-Lopez, Raquel et al.
DOI número
10.1016/j.media.2025.103531
Year
2025
Títol Complet
servicio de un gerente de ensayos clínicos para el proyecto “Investigación operativa contra la desnutrición infantil crónica en Angola” (Proyecto CRESCER)-FED/2020/418-106 de la Fundació Hospital Universitari Vall Hebron - Institut de Recerca (VHIR).
Expedient
GERENTE DE ENSAYOS CLÍNICOS PROYECTO CRESCER
Codi
24980241
Data publicació
Year
2025
Títol Complet
Hiring a service of DNA and RNA sequencing and data analysis from tumor samples and whole blood in the Fundació Hospital Universitari Vall Hebron - Institut de Recerca (VHIR)
Expedient
RNA SEQUENCING (PI23/01045)
Codi
24980240
Data publicació
Year
2025
Títol Complet
Servei extern per la logística de la gestió dels kits d'assaigs clínics per la Unitat de Suport a la Investigació Clínica de la Fundació Hospital Universitari Vall Hebron – Institut de Recerca (VHIR).
Expedient
GESTIÓ KITS DEL ASSAIGS CLÍNICS
Codi
24980239
Data publicació

Professionals

Xana Garcia Fernandez

I am a Biology graduate with a special interest in neglected and parasitic infectious diseases. I am part of the Diagnostic Nanotools group (DINA) at the Vall d'Hebron Research Institute, where we work on the development of new diagnostic techniques for infectious diseases.

A Multi-centered, Double-blind, Randomized, Placebo-controlled, Parallel Group Phase 2 Study of TEV-56286 for the Treatment of Patients with Multiple System Atrophy

  • Protocol code: TV56286-NDG-20039
  • EudraCT code: No aplica
  • Pathology: Malalties del sistema nerviós
  • Principal investigator:  Hernández Vara, Jorge
  • Research group:  Malalties neurodegeneratives
  • Service: Neurologia
  • Phase: Fase II
  • Recruiting: Closed
  • Status: Iniciat

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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 multicéntrico, aleatorizado, doble ciego, controlado con placebo y degrupos paralelos para evaluar la eficacia y la seguridad de dapirolizumab pegol en participantes del estudio con lupus eritematoso sistémico de moderado a grave

  • Protocol code: SL0044
  • EudraCT code: 2019-003407-35
  • Pathology: Símptomes, signes i troballes anormals clíniques i de laboratori, no classificades enlloc més
  • Principal investigator:  Cortes Hernandez, Josefina
  • Research group:  Reumatologia
  • Service: Reumatologia
  • Phase: Fase 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 Fase 2b, multicéntrico, aleatorizado, parcialmentecontrolado con placebo y doble ciego para evaluar la seguridad y eficacia de laadministración secuencial de Daplusiran/Tomligisiran seguido de bepirovirsen enparticipantes con Hepatitis B crónica en tratamiento con análogos de nucleós(t)idos (BUnited).

  • Protocol code: 218309
  • EudraCT code: No aplica
  • 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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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.

An open label complex clinical trial in newly diagnosed pediatric de novo AML patients – a study by the NOPHO-DB-SHIP consortium

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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 EN FASE IB MULTICÉNTRICO, NO ALEATORIZADO,ABIERTO, ADAPTATIVO, CON GRUPOS PARALELOS, DE DOSIS ÚNICAS ASCENDENTES(PARTES 1 Y 2) Y DOSIS MÚLTIPLES ASCENDENTES (PARTE 3) PARA INVESTIGAR LASEGURIDAD, TOLERABILIDAD, INMUNOGENICIDAD, FARMACOCINÉTICA YFARMACODINAMIA DE RO7121932 TRAS ADMINISTRACIÓN POR VÍA INTRAVENOSA(PARTE 1) Y SUBCUTÁNEA (PARTES 2 Y 3) EN PARTICIPANTES CON ESCLEROSISMÚLTIPLE

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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.

Un ensayo multicéntrico, aleatorizado y doble ciego para evaluar laeficacia y la seguridad de PRAX-628 en adultos con crisis focales (POWER 1)

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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.

Optimization of albuminuria lowering therapies to individual patients with CKD using FINErenone and SEmaglutide.

  • Protocol code: 17456 (FINESSE)
  • EudraCT code: _
  • 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 II
  • 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.

ENSAYO EN FASE Ib EN CANASTA SIN ENMASCARAMIENTO DE RAY121 PARA INHIBIR LA VÍA CLÁSICA DEL COMPLEMENTO EN ENFERMEDADES INMUNOLÓGICAS

  • Protocol code: RAY902CT
  • EudraCT code: No aplica
  • Pathology: Symptoms, signs, and abnormal clinical and laboratory findings, not elsewhere classified
  • Principal investigator:  Pardos Gea, José
  • Research group:  Malalties sistèmiques
  • Service: Medicina Interna
  • Phase: Phase I
  • Recruiting: Closed
  • Status: Open

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

PROLONGACIÓN DEL BESTOW: Estudio en fase II, multicéntrico, sinenmascaramiento y de prolongación para evaluar la seguridad y eficacia a largo plazo de tegoprubarten receptores de trasplante de riñón

  • Protocol code: AT-1501-K209
  • EudraCT code: No aplica
  • Pathology: Symptoms, signs, and abnormal clinical and laboratory findings, not elsewhere classified
  • Principal investigator:  Bestard Matamoros, Oriol
  • Research group:  Nephrology and kidney transplantation
  • Service: Nephrology
  • Phase: Phase II
  • Recruiting: Open
  • Status: Open

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I have read and accept the data protection policy *.
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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 en fase 1/2 de determinación de la dosis y ampliación de la dosis de Cobolimab en combinación con Dostarlimab en participantes pediátricos y adultos jóvenes con tumores recién diagnosticados y recidivantes/resistentes al tratamiento

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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.