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ESTUDIO INTERVENCIONAL DE EFICACIA YSEGURIDAD, FASE III, ALEATORIZADO, DOBLE CIEGO,CONTROLADO CON PLACEBO, SEGUIDO DE UN PERIODOABIERTO, PARA INVESTIGAR RIMEGEPANT EN LAPREVENCIÓN DE LA MIGRAÑA EN ADOLESCENTES DE ENTRE12 Y MENOS DE 18 AÑOS DE EDAD CON MIGRAÑA CRÓNICA

  • Protocol code: C4951013
  • EudraCT code: No aplica
  • Pathology: Malalties del sistema nerviós
  • Principal investigator:  Pozo Rosich, Patricia
  • Research group:  Cefalea i dolor neurològic
  • Service: Neurologia
  • 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.

Single-arm open-label trial to assess safety, tolerability, pharmacokinetics, and pharmacodynamics of BI 3000202 in adult patients with selected type 1 interferonopathies.

  • Protocol code: 1509-0003
  • EudraCT code: _
  • Pathology: Símptomes, signes i troballes anormals clíniques i de laboratori, no classificades enlloc més
  • Principal investigator:  Lopez Corbeto, Mireia
  • Research group:  Reumatologia
  • Service: Reumatologia
  • Phase: Fase I
  • 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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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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A phase II study to evaluate DNTH103 in adults with multifocal motor neuropathy (MOMENTUM)

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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 II, aleatorizado, doble ciego y controlado con placebosobre el uso de ensifentrina en pacientes con bronquiectasia no asociada a fibrosisquística.

  • Protocol code: RPL554-NCFB-220
  • EudraCT code: No aplica
  • Pathology: Tumors
  • Principal investigator:  Polverino , Eva
  • Research group:  Pneumologia
  • Service: Pneumologia
  • 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.
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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 
The request for information on a research project or clinical trial does not entail inclusion in it.

Ensayo de fase II, aleatorizado y abierto para comparar el tratamiento endocrino neoadyuvante en combinación con trastuzumab y pertuzumab con o sin el inhibidor de la PI3K inavolisib en pacientes con cáncer de mama precoz RH+/HER2+ con mutación de PIK3CA – GeparPiPPa

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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 
The request for information on a research project or clinical trial does not entail inclusion in it.

Estudio de fase III, aleatorizado, doble ciego, controlado con placebo, para evaluar la eficacia y la seguridad de maralixibat en el tratamiento de participantes con prurito colestásico

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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 
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Interventional, randomized, double-blind, parallel-group, placebo-controlled, dose-finding trial of Lu AG09222 for the prevention of migraine in participants with episodic and chronic migraine.

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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 3, multinacional, aleatorizado, doble ciego ycontrolado con placebo para evaluar la eficacia y la seguridad del treprostinilo inhalado enpacientes con fibrosis pulmonar progresiva (TETON-PPF)

  • Protocol code: RIN-PF-305
  • EudraCT code: No aplica
  • Pathology: Malalties del sistema respiratori
  • Principal investigator:  Villar Gomez, Ana
  • Research group:  Pneumology
  • Service: Pneumology
  • 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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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, de múltiples etapas, multicéntrico,aleatorizado, con un periodo de retirada doble ciego, en gruposparalelos y controlado con placebo,para evaluar la eficacia y laseguridad de nipocalimab administrado a adultos conpolineuropatía desmielinizante inflamatoria crónica (PDIC)

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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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A Phase III Multi-center, Open-label, Sponsor-blinded, Randomized Study of AZD0901 Monotherapy Compared with Investigator’s Choice of Therapy in Second- or Later-Line Adult Participants with Advanced/Metastatic Gastric or Gastroesophageal Junction Adenocarcinoma Expressing Claudin18.2 (CLARITY-Gastric 01)

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Estudio de fase II, aleatorizado, doble ciego, controlado con placebo, degrupos paralelos, con dos brazos para investigar la eficacia, seguridad y tolerabilidad delunsekimig subcutáneo (SAR443765) en participantes adultos con asma de alto riesgo que noson actualmente elegibles para tratamiento biológico.

  • Protocol code: ACT18301
  • EudraCT code: No aplica
  • Pathology: Diseases of the respiratory system
  • Principal investigator:  Romero Mesones, Christian Eduardo
  • Research group:  Pneumology
  • Service: Pneumology
  • 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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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 
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Estudio abierto de fase 2 para evaluar la seguridad, la tolerabilidady la eficacia de NVG-2089 por vía intravenosa en participantes con polineuropatíadesmielinizante inflamatoria crónica (PDIC)

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Controller: Fundació Hospital Universitari Vall Hebron Institut de Recerca – VHIR- G60594009.
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A 2-Part, Randomized, Double-Blind, Placebo-Controlled Study in Participants with Duchenne Muscular Dystrophy Amenable to Exon 44 Skipping to Evaluate the Safety and Efficacy of ENTR-601-44 (ELEVATE-44)

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An Open Label Clinical Trial to Evaluate the Efficacy and Safety of PRAX-628 in Adult Patients with Focal Onset or Primary Generalized Tonic-Clonic Seizures

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Estudio multicéntrico, aleatorizado, doble ciego, de grupos paralelos y controlado conplacebo en el que se evalúan la eficacia y la seguridad de iptacopán (LNP023) en laglomerulonefritis membranoproliferativa idiopática mediada por inmunocomplejos.

  • Protocol code: CLNP023B12302
  • EudraCT code: No aplica
  • Pathology: Symptoms, signs, and abnormal clinical and laboratory findings, not elsewhere classified
  • Principal investigator:  Agraz Pamplona, Irene
  • Research group:  Nefrologia i trasplantament renal
  • Service: Nefrologia
  • 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.
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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An Open-Label Extension Study of EryDex in Patients with Ataxia Telangiectasia Following Participation in Study IEDAT-04-2022 (NEAT)

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Estudio de fase 3 abierto, multicéntrico y aleatorizado para evaluar la eficacia y seguridad de romosozumab en comparación con bisfosfonatos en niños y adolescentes con osteogénesis imperfecta.

  • Protocol code: 20200105
  • EudraCT code: No aplica
  • Pathology: Malalties del sistema osteomuscular i del teixit connectiu
  • Principal investigator:  Campos Martorell, Ariadna
  • Research group:  Creixement i desenvolupament
  • Service: General Pediatrics and Specialties
  • 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 fase 2, aleatorizado, doble ciego, controlado conplacebo, de grupos paralelos de HBV937 en esclerosis lateral amiotrófica (ELA)durante 40 semanas seguido de una extensión abierta

  • Protocol code: CVHB937B12201
  • EudraCT code: No aplica
  • Pathology: Nervous system diseases
  • Principal investigator:  Juntas Morales, Raul
  • Research group:  Peripheral Nervous System
  • Service: Neurology
  • Phase: Phase III
  • Recruiting: Open
  • Status: Open

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Ensayo intervencionista, aleatorizado, con enmascaramientodoble, controlado con placebo y con extensión sinenmascaramiento opcional, de Lu AF82422 en participantes conatrofia multisistémica

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The request for information on a research project or clinical trial does not entail inclusion in it.

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Neda Akhlaghi