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Estudio de fase III multicéntrico, aleatorizado, doble ciego, de grupos paralelos, controlado con placebo y del tiempo hasta la primera exacerbación del asma para evaluar la eficacia y la seguridad de benralizumab en pacientes pediátricos con asma eosinofílica severa

  • Protocol code: D3250C00024
  • EudraCT code: No aplica
  • Pathology: Embaràs, part i puerperi
  • Principal investigator:  de Mir Messa, Inés
  • Research group:  Creixement i desenvolupament
  • Service: Pediatria General i Especialitats
  • Phase: Fase III
  • 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.

Protocolo maestro para investigar la eficacia y la seguridad de LY3437943 una vez a la semana en participantes sin diabetes tipo 2 que tienen obesidad o sobrepeso: ensayo aleatorizado, con doble enmascaramiento y comparativo con placebo

  • Protocol code: J1I-MC-GZBJ
  • EudraCT code: No aplica
  • Pathology: Malalties endocrines, nutricionals i metabòliques
  • Principal investigator:  Ciudin Mihai, Andreea
  • Research group:  Diabetis i metabolisme
  • Service: Endocrinologia
  • 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.

Ensayo de fase 3, multicéntrico, aleatorizado, doble ciego, de grupos paralelos ycontrolado con placebo para evaluar la eficacia, la seguridad y la tolerabilidad de ianalumab en combinación con el tratamiento estándar en participantes con nefritislúpica activa (SIRIUS-LN).

  • Protocol code: CVAY736K12301
  • EudraCT code: 2020-005830-14
  • 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: 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.
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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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Estudio multicéntrico, aleatorizado, con enmascaramiento doble, controlado con placebo y de fase 2 en el que se evalúan la seguridad y la eficacia de CORT113176 (Dazucorilant) en pacientes con esclerosis lateral amiotrófica (DAZALS)

  • Protocol code: CORT113176-652
  • EudraCT code: 2021-005611-31
  • Pathology: Malalties del sistema nerviós
  • Principal investigator:  Juntas Morales, Raul
  • Research group:  Sistema nerviós perifèric
  • Service: Neurologia
  • Phase: Fase II
  • Recruiting: Open
  • 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.
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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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Estudio en fase III, aleatorizado, controlado con placebo y doble ciego de darolutamida más tratamiento de privación de andrógenos (TPA) en comparación con placebo más TPA en pacientes con cáncer de próstata con recurrencia bioquímica (RB) de alto riesgo

  • Protocol code: 21492
  • EudraCT code: 2022-000793-26
  • Pathology: Tumors
  • Principal investigator:  Maldonado Pijoan, Javier
  • Service: Oncologia Radioteràpica
  • Phase: Phase III
  • Recruiting: Closed
  • Status: Open

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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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Estudio de fase 3, aleatorizado, doble ciego para investigar la eficacia y la seguridad de LY3437943 administrado una vez a la semana en comparación con placebo en participantes con obesidad severa y con enfermedad cardiovascular establecida

  • Protocol code: J1I-MC-GZBM
  • EudraCT code: No aplica
  • Pathology: Endocrine, nutritional and metabolic diseases
  • Principal investigator:  Ciudin Mihai, Andreea
  • Research group:  Diabetes and Metabolism
  • Service: Endocrinology
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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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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Estudio de fase 2, aleatorizado, doble ciego, multicéntrico y controlado con placebo para evaluar la seguridad y tolerabilidad de treprostinil palmitilo en polvo para inhalación en pacientes con hipertensión pulmonar asociada a enfermedad pulmonar intersticial

  • Protocol code: INS1009-211
  • EudraCT code: 2021-003294-66
  • Pathology: Malalties del sistema respiratori
  • Principal investigator:  Ojanguren Arranz, Iñigo
  • Research group:  Pneumologia
  • Service: Pneumologia
  • Phase: Phase II
  • Recruiting: Open
  • Status: Tancat

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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.
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RAvulizumab to PRotect PaTients with Chronic Kidney DisEase (CKD) froM Cardiac Surgery Associated Acute Kidney Injury (CSA-AKI) and Subsequent Major Adverse Kidney Events (MAKE): A Phase 3, Randomized, Double-blind, Placebo-controlled, Multicenter Study

  • Protocol code: ALXN1210-CSA-AKI-318
  • EudraCT code: No aplica
  • Pathology: Symptoms, signs, and abnormal clinical and laboratory findings, not elsewhere classified
  • Principal investigator:  Ferrer Roca, Ricard
  • Research group:  Shock, disfunció orgànica i ressuscitació
  • Service: UCI (servei de cures intensives)
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Un estudio abierto y a largo plazo para evaluar la seguridad y la eficacia de aticaprant como tratamiento complementario en participantes adultos y de edad avanzada con trastorno depresivo mayor (TDM).

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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 Multicéntrico, Aleatorizado, Doble Ciego y Controlado con Placebo para evaluar la eficacia y la seguridad de la rifaximina en comprimidos de Dispersión Sólida Soluble (SSD) para el retraso de la Descompensación de la Encefalopatía en la Cirrosis (Red-C)

  • Protocol code: RNLC3132
  • EudraCT code: No aplica
  • Pathology: Symptoms, signs, and abnormal clinical and laboratory findings, not elsewhere classified
  • Principal investigator:  Simon-Talero Horga, Macarena
  • Research group:  Malalties hepàtiques
  • Service: Hepatologia
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Controller: Fundació Hospital Universitari Vall Hebron Institut de Recerca – VHIR- G60594009.
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Estudio de extensión abierto de JM-010 en pacientes con enfermedad de Parkinson con disquinesia

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BHV3000-406: Ensayo en fase IV, aleatorizado, doble ciego, controlado con placebo, para evaluar la eficacia y tolerabilidad de rimegepant para el tratamiento agudo de la migraña en adultos no aptos para el uso de triptanes

  • Protocol code: BHV3000-406
  • EudraCT code: 2022-001175-14
  • Pathology: Nervous system diseases
  • Principal investigator:  Pozo Rosich, Patricia
  • Research group:  Cefalea i dolor neurològic
  • Service: Neurology
  • Phase: Fase IV
  • Recruiting: Open
  • Status: Open

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Estudio de fase 1/2, abierto y de un solo brazo, que evalúa la seguridad y eficacia del ponatinib para el tratamiento de leucemias o tumores sólidos recurrentes o refractarios en pacientes pediátricos

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Estudio clínico aleatorizado, doble ciego y controlado con placebo para evaluar mavacamten en adultos con cardiomiopatía hipertrófica sintomática no obstructiva

  • Protocol code: CV027-031
  • EudraCT code: 2021-005329-26
  • Pathology: Malalties del sistema circulatori
  • Principal investigator:  Limeres Freire, Javier
  • Research group:  Malalties cardiovasculars
  • Service: Cardiologia
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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ESTUDIO DE FASE III, ALEATORIZADO, DOBLE CIEGO Y CONTROLADO CON PLACEBO PARA EVALUAR ATEZOLIZUMAB Y BEVACIZUMAB, CON O SIN TIRAGOLUMAB, EN PACIENTES CON CARCINOMA HEPATOCELULAR LOCALMENTE AVANZADO O METASTÁSICO NO TRATADO.

  • Protocol code: CO44668
  • EudraCT code: No aplica
  • Pathology: Tumors
  • Principal investigator:  Minguez Rosique, Beatriz
  • Research group:  Liver Diseases
  • Service: Hepatology
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Estudio en fase III, aleatorizado, con doble enmascaramiento y controlado con principio activo para evaluar la eficacia y la seguridad de aflibercept 8 mg en el edema macular secundario a oclusión venosa retiniana.

  • Protocol code: 22153
  • EudraCT code: No aplica
  • Pathology: Malalties de l’ull i dels seus annexos
  • Principal investigator:  Garcia-Arumí Fusté, Claudia
  • Research group:  Oftalmologia
  • Service: Oftalmologia
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Un estudio aleatorizado, doble ciego, multicéntrico, de grupos paralelos y controlado con placebo para evaluar la eficacia, la seguridad y la tolerabilidad de aticaprant 10 mg como tratamiento complementario en participantes adultos con trastorno depresivo mayor (TDM) con anhedonia moderada a grave y una respuesta insuficiente al tratamiento antidepresivo actual.

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A multi-center, randomized, double-blind, placebo controlled, parallel-group PhaseIIIb study evaluating the effect of inclisiran on atherosclerotic plaque progressionassessed by coronary computed tomography angiography (CCTA) in participantswith a diagnosis of non-obstructive coronary artery disease without previouscardiovascular events

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Extensión a largo plazo del ensayo ARGX-117-2002 para evaluar la seguridad y la tolerabilidad, la eficacia, la farmacodinámica, la farmacocinética y la inmunogenicidad a largo plazo de ARGX-117 en adultos con neuropatía motora multifocal

  • Protocol code: ARGX-117-2003
  • EudraCT code: 2021-004998-32
  • Pathology: Nervous system diseases
  • Principal investigator:  Juntas Morales, Raul
  • Research group:  Peripheral Nervous System
  • Service: Neurology
  • 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.

Comparación del rendimiento y la seguridad de T2769 frente a Vismed® Multi en el tratamiento del síndrome del ojo seco de moderado a grave.

  • Protocol code: LT2769-002
  • EudraCT code: No aplica
  • Pathology: Diseases of the eye and its adnexa
  • Principal investigator:  Pueyo Ferrer, Alfredo
  • Research group:  Ophtalmology
  • Service: Ophthalmology
  • Phase: Phase I
  • Recruiting: Open
  • Status: Open

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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.