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A Phase I/II study of Brigatinib in pediatric and young adult patients with ALK+ Anaplastic Large Cell Lymphoma, Inflammatory Myofibroblastic Tumors or other solid tumors

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Controller: Fundació Hospital Universitari Vall Hebron Institut de Recerca – VHIR- G60594009.
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Estudio de fase IIb pivotal para evaluar la eficacia y la seguridad de izokibep en sujetos con uveítis intermedia, posterior , no infecciosa o panuveítis

  • Protocol code: 21103
  • EudraCT code: 2021-006498-49
  • Pathology: Malalties de l’ull i dels seus annexos
  • Principal investigator:  Distefano , Laura Natalia
  • Research group:  Oftalmologia
  • Service: Oftalmologia
  • Phase: Phase II
  • Recruiting: Closed
  • 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.
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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 pivotal de fase III multicéntrico, aleatorizado, doble ciego y comparado con placebo sobre la eficacia y la seguridad de DMX-200 en pacientes con glomeruloesclerosis focal y segmentaria (GEFS) que estén en tratamiento con un antagonista de los receptores de la angiotensina II (ARA-II)

  • Protocol code: DMX-200-301
  • EudraCT code: 2021-004174-64
  • 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: 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.
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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 PLATAFORMA EN FASE II DE INMUNO-ONCOLOGÍA DE PRECISIÓN CON INDICACIÓN TUMOR AGNÓSTICA PARA MUTACIONES SOMÁTICAS ESPECÍFICAS (TAPISTRY)

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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 en fase III, doble ciego, aleatorizado y controlado con placebo del tratamiento adyuvante con ganaxolona (GNX) en niños y adultos con epilepsia relacionada con el complejo de esclerosis tuberosa (CET) (TrustTSC)

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Controller: Fundació Hospital Universitari Vall Hebron Institut de Recerca – VHIR- G60594009.
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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 
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Ensayo clínico, prospectivo de fase IV, de un solo brazo para evaluar con Monitorización Continua de Glucosa (MCG) la eficacia y seguridad del cambio a Glargina-300 desde Glargina-100 en pacientes con Diabetes Mellitus tipo 2 (DM2) e insuficiencia renal.

  • Protocol code: LPS17375
  • EudraCT code: 2021-005353-82
  • Pathology: Malalties endocrines, nutricionals i metabòliques
  • Principal investigator:  Simó Servat, Olga
  • Research group:  Diabetis i metabolisme
  • Service: Endocrinologia
  • Phase: Fase IV
  • Recruiting: Open
  • Status: Open

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Controller: Fundació Hospital Universitari Vall Hebron Institut de Recerca – VHIR- G60594009.
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Estudio demostrativo preliminar de fase IIa, multicéntrico, aleatorizado, abierto y controlado para evaluar la eficacia, seguridad y tolerabilidad de VS-01 además del tratamiento estándar, en comparación con el tratamiento estándar solo, en pacientes adultos con insuficiencia hepática crónica agudizada (IHCA) de grado 1-2 y ascitis

  • Protocol code: VS01-IIa-01
  • EudraCT code: 2021-002617-33
  • Pathology: Tumors
  • Principal investigator:  Campos Varela, Isabel
  • Research group:  Malalties hepàtiques
  • Service: Hepatologia
  • Phase: Phase II
  • Recruiting: Closed
  • Status: Tancat

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Estudio de fase IV, multicéntrico, aleatorizado, doble ciego y controlado con placebo de la eficacia, seguridad, tolerabilidad y calidad de vida de un tratamiento en curso hipolipemiante, optimizado individualmente, con o sin inclisirán (KJX839), en participantes con hipercolesterolemia.

  • Protocol code: CKJX839A12402
  • EudraCT code: 2021-003759-40
  • Pathology: Factors que influencien en l’estat de salut i contacte amb els serveis de salut
  • Principal investigator:  Urquizu Padilla, Maria
  • Service: Medicina Interna
  • Phase: Phase IV
  • Recruiting: Open
  • Status: Open

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Controller: Fundació Hospital Universitari Vall Hebron Institut de Recerca – VHIR- G60594009.
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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 en fase II/III, multicéntrico, aleatorizado, doble ciego, para evaluar la eficacia, la seguridad, la farmacocinética y la farmacodinámica de ozanimod por vía oral (RPC1063) en participantes pediátricos con enfermedad de Crohn de moderada a intensamente activa con una respuesta inadecuada al tratamiento convencional

  • Protocol code: IM047-023
  • EudraCT code: 2021-005019-30
  • Pathology: Malalties del sistema digestiu
  • Principal investigator:  Segarra Canton, Oscar
  • Research group:  Recerca en microbioma
  • Service: Pediatria General i Especialitats
  • Phase: Phase III
  • Recruiting: Closed
  • Status: Open

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Controller: Fundació Hospital Universitari Vall Hebron Institut de Recerca – VHIR- G60594009.
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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.
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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 intervencionista, aleatorizado, doble ciego, de grupos paralelos y controlado con placebo, de tratamiento con eptinezumab añadido a una breve intervención educativa para el tratamiento preventivo de las migrañas en pacientes con un doble diagnóstico de migraña y cefalea por abuso de medicamentos

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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 II, doble ciego, aleatorizado, de múltiples dosis, cruzado, de tres tratamientos, tres períodos y seis secuencias, controlado con placebo, para evaluar la eficacia, farmacocinética, farmacodinámica, la seguridad y la tolerabilidad de bromuro de glicopirronio en niños con asma de 6 a menos de 12 años de edad

  • Protocol code: CQVM149C2201
  • EudraCT code: 2021-004972-32
  • Pathology: Malalties del sistema respiratori
  • Principal investigator:  Garriga Baraut, Maria Teresa
  • Research group:  Creixement i desenvolupament
  • Service: General Pediatrics and Specialties
  • Phase: Phase II
  • Recruiting: Open
  • Status: Open

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Estudio en fase II, multicéntrico y sin enmascaramiento para evaluar la eficacia y la seguridad de la monoterapia con Olaparib y la combinación de Olaparib junto con Durvalumab como tratamiento neoadyuvante en pacientes con mutaciones BRCA y cáncer de mama HER2 negativo en fase temprana (OlympiaN)

  • Protocol code: D931CC00001
  • EudraCT code: 2021-005231-22
  • Pathology: Tumors
  • Principal investigator:  Pimentel , Isabel
  • Service: Oncologia
  • Phase: Phase II
  • Recruiting: Open
  • Status: Open

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Estudio de fase III, abierto, controlado, aleatorizado y multicéntrico para comparar la imlifidasa y el tratamiento estándarfrente al tratamiento estándar solo en el tratamiento de la enfermedad grave por anticuerpos anti-MBG (enfermedad deGoodpasture)

  • Protocol code: 21-HMedIdeS-24
  • EudraCT code: No aplica
  • 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: Closed
  • Status: Open

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Estudio aleatorizado, con enmascaramiento doble, comparativo con un placebo, para evaluar la seguridad y la eficacia del PC945 nebulizado cuando se añade a una terapia antifúngica sistémica para el tratamiento dela aspergilosis pulmonar invasiva resistente al tratamiento

  • Protocol code: PC_ASP_006
  • EudraCT code: 2021-004554-32
  • Pathology: Certes malalties infeccioses i parasitàries
  • Principal investigator:  Len Abad, Oscar
  • Research group:  Malalties infeccioses
  • Service: Infeccioses
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Estudio de extensión con tratamiento activo, prospectivo, a largo plazo y de intervención para evaluar la seguridad y la tolerabilidad de NBI-921352 como tratamiento complementario en sujetos con Crisis Epilépticas Focales (CEF)

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Estudio con enmascaramiento doble, controlado con placebo, de aumento progresivo de la dosis ara evaluar la eficacia, la seguridad y la farmacocinética de la voclosporina en adolescentes con nefritis lúpica

  • Protocol code: AUR-VCS-2020-03
  • EudraCT code: 2020-005807-37
  • 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: Closed
  • Status: Open

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ESTUDIO PROSPECTIVO, ALEATORIZADO, ABIERTO, EN FASE II PARA EVALUAR LA SUPERIORIDAD DE INOTUZUMAB OZOGAMICINA EN MONOTERAPIA FRENTE A ALLR3 PARA EL TRATAMIENTO DE INDUCCIÓN DE LA LEUCEMIA LINFOBLÁSTICA AGUDA INFANTIL DE PRECURSORES DE CÉLULAS B EN PRIMERA RECIDIVA DE ALTO RIESGO

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Estudio de fase 3, multicéntrico, aleatorizado, sin enmascaramiento, con grupos paralelos, para evaluar la eficacia y la seguridad de LY3209590 en comparación con la insulina degludec en participantes con diabetes de tipo 2 actualmente tratados con insulina basal (QWINT-3)

  • Protocol code: I8H-MC-BDCU
  • EudraCT code: 2021-002569-16
  • Pathology: Tumors
  • Principal investigator:  Ciudin Mihai, Andreea
  • Research group:  Diabetes and Metabolism
  • Service: Endocrinology
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Estudio de fase I/II con aumento escalonado y ampliación de la dosis, multicéntrico, abierto y con un solo grupo, para evaluar la seguridad, la tolerabilidad, las características farmacocinéticas y la actividad antitumoral de FCN-159 en participantes adultos y menores de edad con neurofibromatosis de tipo 1

  • Protocol code: FCN-159-002
  • EudraCT code: 2021-001572-42
  • Pathology: Nervous system diseases
  • Principal investigator:  Camprodon Gomez, Maria
  • Research group:  Malalties neurodegeneratives
  • Service: Internal Medicine
  • Phase: Phase II
  • Recruiting: Closed
  • Status: Open

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Controller: Fundació Hospital Universitari Vall Hebron Institut de Recerca – VHIR- G60594009.
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ESTUDIO DE FASE 2, MULTICÉNTRICO, ALEATORIZADO, DOBLE CIEGO Y CONTROLADO CON PLACEBO PARA EVALUAR LA EFICACIA Y LA SEGURIDAD DE DAXDILIMAB EN PARTICIPANTES ADULTOS CON NEFRITIS LÚPICA PROLIFERATIVA ACTIVA

  • Protocol code: HZNP-DAX-203
  • EudraCT code: 2022-001377-31
  • 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: Closed
  • Status: Open

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