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Ensayo clínico de fase 2a, aleatorizado, doble ciego, controlado con placebo, para evaluar la seguridad y la eficacia de CM-101 en sujetos con colangitis esclerosante primaria

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  • Protocol code: CM-101-PSC-101
  • EudraCT code: 2019-002945-39
  • Pathology: Factors que influencien en l’estat de salut i contacte amb els serveis de salut
  • Principal investigator:  Campos Varela, Isabel
  • Research group:  Malalties hepàtiques
  • Service: Hepatologia
  • 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.
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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.

Evaluación aleatoria prospectiva de nuevos tratamientos emergentes para la profilaxis de infecciones en el reemplazo total de articulaciones: un estudio piloto (PREVENT-iT)

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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 II, de grupos paralelos, doble ciego y con tres grupos de tratamiento, para evaluar la eficacia y la seguridad de finerenona más empagliflozina en comparación con finerenona o empagliflozina en participantes con enfermedad renal crónica y diabetes tipo 2.

Contact
  • Protocol code: BAY 94-8862 21839
  • EudraCT code: 2021-003037-11
  • Pathology: Malalties endocrines, nutricionals i metabòliques
  • Principal investigator:  Soler Romeo, Maria Jose
  • Research group:  Nefrologia i trasplantament renal
  • Service: Nefrologia
  • Phase: Fase II
  • Recruiting: Open
  • Status: Tancat

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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 de fase 1b, multicéntrico y abierto para evaluar la seguridad, la tolerabilidad, la farmacocinética y la eficacia de mezagitamab (TAK-079) combinado con el tratamiento de fondo estable en pacientes con nefropatía por IgA primaria

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  • Protocol code: TAK-079-1006
  • EudraCT code: 2021-005023-20
  • 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 I
  • Recruiting: Open
  • 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 de fase III, doble ciego, controlado con placebo que evalúa la eficacia y seguridad de ISIS 721744 en pacientes con angioedema hereditario (AEH)

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  • Protocol code: ISIS 721744-CS5
  • EudraCT code: 2021-002571-19
  • Pathology: Símptomes, signes i troballes anormals clíniques i de laboratori, no classificades enlloc més
  • Principal investigator:  Guilarte Clavero, Mar
  • Research group:  Malalties sistèmiques
  • Service: Medicina Interna
  • Phase: Fase III
  • Recruiting: Open
  • 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.
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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 INTERVENCIONAL DE EFICACIA Y SEGURIDAD, DE FASE II, ALEATORIZADO, DOBLE CIEGO, DE TRES GRUPOS PARA INVESTIGAR NIRMATRELVIR/RITONAVIR EN PARTICIPANTES INMUNOCOMPROMETIDOS, NO HOSPITALIZADOS, DE AL MENOS 12 AÑOS DE EDAD CON COVID-19 SINTOMÁTICO

Contact
  • Protocol code: C4671034
  • EudraCT code: 2022-001362-35
  • Pathology: Certes malalties infeccioses i parasitàries
  • Principal investigator:  Len Abad, Oscar
  • Research group:  Malalties infeccioses
  • Service: Infeccioses
  • Phase: Fase II
  • Recruiting: Open
  • Status: Tancat

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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 de fase 2/3, multicéntrico, doble ciego y aleatorizado para determinar la eficacia y la seguridad de DNL310 frente a idursulfasa en participantes pediátricos con mucopolisacaridosis neuronopática o no neuronopática de tipo II.

Contact
  • Protocol code: DNLI-E-0007
  • EudraCT code: 2021-005200-35
  • Pathology: Malalties del sistema nerviós
  • Principal investigator:  Del Toro Riera, Mireia
  • Research group:  Neurologia pediàtrica
  • Service: Pediatria General i Especialitats
  • Phase: Fase II
  • Recruiting: Open
  • 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.

LOGGIC/FIREFLY-2: Ensayo en fase III, aleatorizado, internacional y multicéntrico de DAY101 en monoterapia frente a la quimioterapia estándar en pacientes con glioma pediátrico de bajo grado que presentan una alteración de RAF activadora que requiere tratamiento sistémico de primera línea

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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 de fase III, multicéntrico, aleatorizado, doble ciego, de grupos paralelos y controlado con placebo en el que se evalúan la eficacia, la seguridad y la tolerabilidad de dos pautas posológicas de ianalumab en combinación con el tratamiento de referencia en pacientes con lupus eritematoso sistémico (SIRIUS-SLE 1).

Contact
  • Protocol code: CVAY736F12301
  • EudraCT code: 2022-002691-36
  • 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: Iniciat

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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.

Odevixibat (A4250) in children with biliary atresia (BOLD-EXT)

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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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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.
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