What are you looking for? Write the name, title or any keyword related to what you are looking for and select which content category it belongs to. Search Fulltext search Activities Professionals Research groups News - Any - 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) Contact Protocol code: ENTR-601-44-201 EudraCT code: 2024-517584-23-00 Pathology: Duchenne muscular dystrophy Pharmac: Hydrocortisone Promoter: Entrada Theraputics, Inc. Principal investigator: Gómez Andrés, David Research group: Teràpies i Innovació en Neuropediatria i altres malalties rares pediàtriques. Service: Neurologia pediàtrica Phase: Fase I Recruiting: Open Status: Activo Contact Form Name* First surname* Second surname Email address* Telephone* Write your question* I have read and accept the data protection policy *. 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. Estudio de tolerabilidad y aceptación de dos fórmulas magistrales de hidrocortisona oral para pediatría Contact Protocol code: HIDROGUM21 EudraCT code: 2021-001069-20 Pathology: Adrenal hyperplasia or isolated primary adrenal insufficiency or panhypopituitarism (secondary or tertiary adrenal insufficiency). Promoter: Hospital Universitario Vall Hebron Principal investigator: Parramon Teixido, Carlos Javier Research group: Recerca en farmacia bàsica, translacional i clínica Service: Farmàcia Phase: Fase IV Recruiting: Open Status: Activo Contact Form Name* First surname* Second surname Email address* Telephone* Write your question* I have read and accept the data protection policy *. 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. Recombination Chimeric Monoclonal Antibody CH.14.18 Contact Protocol code: SIOPENRNET002 EudraCT code: 2006-001489-17 Pathology: Neuroblastoma Pharmac: Anticuerpo monoclonal recombinante antiGDch14.18. Promoter: Dra. Victoria Castel (Hospital La Fe de Valencia) Principal investigator: Moreno Martín-Retortillo, Lucas Research group: Càncer i malalties hematològiques infantils Service: Oncohematologia Pediàtrica Phase: Fase III Recruiting: Open Status: Activo Contact Form Name* First surname* Second surname Email address* Telephone* Write your question* I have read and accept the data protection policy *. 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. A phase III, Multicenter, Randomized, Double-blind Study to Assess Efficacy and Safety of Two Doses of Crizanlizumab versus placebo, with or without Hydroxyurea/ Hydroxycarbamide Therapy, in Adolescent and Adult Sickle Cell Disease Patients with Vaso-Occlusive Crises (STAND) Contact Protocol code: CSEG101A2301 EudraCT code: 2017-001746-10 Pathology: Sickle cell disease Pharmac: Crizanlizumab Promoter: Novartis Pharma AG Principal investigator: Beneitez Pastor, David Research group: VHIO (Grups bàsics i clínics) Service: Hematologia Phase: Phase III Recruiting: Closed Status: Finalizado Contact Form Name* First surname* Second surname Email address* Telephone* Write your question* I have read and accept the data protection policy *. 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. Estudio en fase III, aleatorizado, abierto, con control activo, multicéntrico, para evaluar la eficacia y la seguridad de crovalimab frente a eculizumab en pacientes adultos y adolescentes con hemoglobinuria paroxística nocturna (HPN) actualmente tratada con inhibidores del complemento Contact Protocol code: BO42161 EudraCT code: 2020-000597-26 Pathology: Paroxysmal Nocturnal Hemoglobinuria (PNH) Pharmac: CROVALIMAB Promoter: F. Hoffmann-La Roche AG (Switzerland) Principal investigator: Beneitez Pastor, David Research group: VHIO (Grups bàsics i clínics) Service: Hematologia Phase: Phase III Recruiting: Closed Status: Finalizado Contact Form Name* First surname* Second surname Email address* Telephone* Write your question* I have read and accept the data protection policy *. 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. Estudio de fase 3, multicéntrico, aleatorizado, doble ciego, controlado con placebo y de grupos paralelos con una extensión abierta para evaluar la eficacia y la seguridad de rilzabrutinib por vía oral (PRN1008) en adultos y adolescentes con trombocitopenia inmunitaria (TPI) persistente o crónica Contact Protocol code: PRN1008-018 EudraCT code: 2020-002063-60 Pathology: Immune Thrombocytopenia (ITP) Pharmac: Rilzabrutinib (PRN1008) Promoter: Principia Biopharma Inc. (United States) Principal investigator: Valcarcel Ferreiras, David Research group: VHIO (Grups bàsics i clínics) Service: Hematologia Phase: Phase III Recruiting: Closed Status: Finalizado Contact Form Name* First surname* Second surname Email address* Telephone* Write your question* I have read and accept the data protection policy *. 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. Ensayo multinacional, abierto, aleatorizado y controlado para investigar la eficacia y la seguridad de NNC0365-3769 (Mim8) en adultos y adolescentes con hemofilia A con o sin inhibidores Contact Protocol code: NN7769-4514 EudraCT code: 2020-001048-24 Pathology: Hemofilia A con inhibidores Pharmac: NNC0365-3769 (Mim8) Promoter: Novo Nordisk A/S Principal investigator: Benitez Hidalgo, Olga Research group: VHIO (Grups bàsics i clínics) Service: Hematologia Phase: Phase III Recruiting: Closed Status: Cerrado Contact Form Name* First surname* Second surname Email address* Telephone* Write your question* I have read and accept the data protection policy *. 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. Estudio abierto para investigar la eficacia, la seguridad y la farmacocinética de la profilaxis con concizumab en niños menores de 12 años con hemofilia A o B con o sin inhibidores Contact Protocol code: NN7415-4616 EudraCT code: 2020-000504-11 Pathology: Haemophilia A or B with or without inhibitors Pharmac: Concizumab Promoter: Novo Nordisk A/S Principal investigator: Benitez Hidalgo, Olga Research group: VHIO (Grups bàsics i clínics) Service: Hematologia Phase: Phase III Recruiting: Open Status: Activo Contact Form Name* First surname* Second surname Email address* Telephone* Write your question* I have read and accept the data protection policy *. 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. A phase 3b open-label, multicenter study evaluating physicalactivity and joint health in previously treated patients =12 years of age with severehaemophilia A treated with intravenous recombinant coagulation factor VIII FcvonWillebrand Factor-XTEN fusion protein (rFVIIIFc-VWF-XTEN; efanesoctocogalfa) for 24 months. Contact Protocol code: BIVV001-001 EudraCT code: 2022-500275-31-00 Pathology: Haemophilia A Pharmac: Recombinant Coagulation Factor VIII Fc-von Willebrand Factor-XTEN Fusion Protein (rFVIIIFc-VWF-XTEN; BIVV001) Promoter: Swedish Orphan Biovitrum AB (publ) (Sweden) Principal investigator: Benitez Hidalgo, Olga Research group: VHIO (Grups bàsics i clínics) Service: Hematologia Phase: Phase III Recruiting: Closed Status: Finalizado Contact Form Name* First surname* Second surname Email address* Telephone* Write your question* I have read and accept the data protection policy *. 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. Estudio de dosis escalonadas para evaluar la farmacocinética, eficacia y seguridad de apotransferrina en pacientes con atransferrinemia. Contact Protocol code: MD2009.04 EudraCT code: 2009-017409-13 Pathology: Congenital atransferrinaemia/ hypotransferrinaemia Pharmac: Apotransferrin Promoter: Sanquin Plasma Products BV Principal investigator: Díaz de Heredia Rubio, Maria Cristina Research group: Childhood Cancer and Blood Disorders Service: Pediatric Oncohematology Phase: Fase II Recruiting: Open Status: Activo Contact Form Name* First surname* Second surname Email address* Telephone* Write your question* I have read and accept the data protection policy *. 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. Estudio fase1/2, abierto, multicentrico, first in human para evualar la seguridad, tolerabilidad, pk y actividad atnitumoral de repotrectinib (TPX-0005) en pacientes con TSA y reordenamiento ALK, ROS1, o NTRK1-3 Rearrangements (TRIDENT-1) Contact Protocol code: TPX-0005-01 EudraCT code: 2016-003616-13 Pathology: Advanced solid tumors Pharmac: TPX-0005 Promoter: Turning Point Therapeutics, Inc. Principal investigator: Felip Font, Enriqueta Research group: VHIO (Grups bàsics i clínics) Service: Oncologia Phase: Phase I Recruiting: Open Status: Activo Contact Form Name* First surname* Second surname Email address* Telephone* Write your question* I have read and accept the data protection policy *. 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. Estudio fase 1b, abierto, de un solo brazo de tratamiento con Epcoritamab en pacientes pediátricos con neoplasias de células B maduras recidivantes/refractarias. Contact Protocol code: M20-429 EudraCT code: 2021-004555-16 Pathology: Relapsed/Refractory Aggressive Mature B-cell Neoplasms Pharmac: Epcoritamab Promoter: AbbVie Deutschland GmbH & Co. KG Principal investigator: Hladun Alvaro, Raquel Research group: Childhood Cancer and Blood Disorders Service: Pediatric Oncohematology Phase: Phase I Recruiting: Closed Status: Cerrado Contact Form Name* First surname* Second surname Email address* Telephone* Write your question* I have read and accept the data protection policy *. 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. FaR-RMS – Un estudio global para niños y adultos con Rabdomiosarcoma recién diagnosticado y recidivante Contact Protocol code: RG_17-247 EudraCT code: 2018-000515-24 Pathology: Rhabdoyosarcoma Pharmac: Irinotecan with IVA (IrIVA). Promoter: University of Birmingham Principal investigator: Hladun Alvaro, Raquel Research group: Childhood Cancer and Blood Disorders Service: Pediatric Oncohematology Phase: Phase I Recruiting: Open Status: Activo Contact Form Name* First surname* Second surname Email address* Telephone* Write your question* I have read and accept the data protection policy *. 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. Ensayo fase 1 / 2 para evaluar la seguridad y la eficacia de AZD0486 en pacientes adolescentes y adultos con leucemia linfoblástica aguda de células B en recaída o refractarios. Contact Protocol code: D7405C00001 EudraCT code: 2023-505840-20-00 Pathology: B-Cell Acute Lymphoblastic Leukaemia Pharmac: AZD0486 Promoter: Astrazeneca AB (Sweden) Principal investigator: Barba Suñol, Pere Research group: Hematologia Experimental Service: Hematologia Phase: Phase I Recruiting: Open Status: Activo Contact Form Name* First surname* Second surname Email address* Telephone* Write your question* I have read and accept the data protection policy *. 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. Estudio en fase III, aleatorizado, doble ciego, controlado con placebo y de dosis única para evaluar la eficacia y la seguridad de suvratoxumab en adultos y adolescentes con ventilación mecánica para la prevención de la neumonía nosocomial Contact Protocol code: AR-320-003 EudraCT code: 2021-004979-14 Pathology: Prevención de la neumonía nosocomial Pharmac: Suvratoxumab Promoter: Aridis Pharmaceuticals Principal investigator: Ferrer Roca, Ricard Research group: Shock, Disfunció Orgànica i Ressucitació Service: UCI Phase: Phase III Recruiting: Closed Status: Cerrado Contact Form Name* First surname* Second surname Email address* Telephone* Write your question* I have read and accept the data protection policy *. 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. Protocolo NOPHO-DBH AML 2012 Estudio de investigación para el tratamiento de niños y adolescentes con leucemia mieloide aguda de 0 a 18 años. Contact Protocol code: NOPHO-DBH-AML-2012 EudraCT code: 2012-002934-35 Pathology: Acute Myeloid Leukemia (Pediatric 0-18 years) Pharmac: NOPHO-DBH AML 2012 Protocol Promoter: Västra Götaland Regionen Principal investigator: Murillo Sanjuán , Laura Research group: Childhood Cancer and Blood Disorders Service: Oncohematologia Ped. Phase: Phase III Recruiting: Closed Status: Finalizado Contact Form Name* First surname* Second surname Email address* Telephone* Write your question* I have read and accept the data protection policy *. 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. Ensayo abierto de extensión para evaluar la seguridad a largo plazo de ZX008 (clorhidrato de fenfluramina) en solución oral como tratamiento adyuvante para convulsiones en pacientes con trastornos infrecuentes de convulsiones tales como encefalopatías epilépticas incluidos el síndrome de Dravet y el síndrome de Lennox-Gastaut Contact Protocol code: ZX008-1900 EudraCT code: 2019-001331-31 Pathology: Dravet syndrome or Lennox-Gastaut syndrome Pharmac: ZX008 (Fenfluramine Hydrochloride) Promoter: Zogenix Principal investigator: Toledo Argany, Manuel Research group: Grup de recerca de l'estat epilèptic i crisis agudes Service: Neurologia Phase: Phase III Recruiting: Closed Status: Cerrado Contact Form Name* First surname* Second surname Email address* Telephone* Write your question* I have read and accept the data protection policy *. 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. A Phase 3, Multicenter, 12-Week, Double-Blind,Placebo Controlled Study to Evaluate the Safety and Efficacy of Atogepant for the Preventive Treatment of Episodic Migraine in Pediatric Subjects 6 to 17 years of age/ Estudio de fase 3, multicéntrico, de 12 semanas, doble ciego y controlado con placebo para evaluar la seguridad y eficacia de Atogepant para el tratamiento preventivo de la migraña episódica en sujetos pediátricos de 6 a 17 años de edad Contact Protocol code: M21-201 EudraCT code: 2022-501100-94-00 Pathology: Episodic Migraine Pharmac: Atogepant Promoter: Abbvie Principal investigator: Pozo Rosich, Patricia Research group: Cefalea i dolor neurològic Service: Neurology Phase: Phase III Recruiting: Open Status: Activo Contact Form Name* First surname* Second surname Email address* Telephone* Write your question* I have read and accept the data protection policy *. 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. Estudio multicéntrico, abierto, de extensión para evaluar la seguridad a largo plazo de Atogepant en sujetos pediátricos de 6 a 17 años de edad con migraña episódica/ A Multicenter, Open-label, Extension Study to Evaluate the Long-term Safety of Atogepant in Pediatric Subjects 6 to 17 years of age with Episodic Migraine Contact Protocol code: M21-199 EudraCT code: 2022-501099-24-00 Pathology: Migraña Pharmac: Atogepant Promoter: Abbvie Principal investigator: Pozo Rosich, Patricia Research group: Headache and Neurological Pain Service: Neurology Phase: Phase III Recruiting: Open Status: Activo Contact Form Name* First surname* Second surname Email address* Telephone* Write your question* I have read and accept the data protection policy *. 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. Estudio fase 3 prospectivo, abierto, multicéntrico y de extensión de los estudios Fase 3, para evaluar la seguridad y tolerabilidad a largo plazo de Soticlestat como tratamiento adyuvante en pacientes con Síndrome Dravet o Síndrome de Lennox-Gastaut (ENDYMION 2) Contact Protocol code: TAK-935-3003 EudraCT code: 2021-002482-17 Pathology: Dravet and Lennox-Gastaut Syndromes Pharmac: Soticlestat Promoter: Takeda Principal investigator: Abraira del Fresno, Laura Research group: Research Group on Status Epilepticus and Acute Seizures Service: Neurology Phase: Phase III Recruiting: Closed Status: Cerrado Contact Form Name* First surname* Second surname Email address* Telephone* Write your question* I have read and accept the data protection policy *. 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. Pagination First page « Previous page ‹ … Page 271 Page 272 Current page 273 Page 274 Page 275 … Next page › Last page »
