ESTUDIO SAINT I (STROKE-ACUTE ISCHEMIC-NXY TRATAMENT). ESTUDIO DOBLE CIEGO, ALEATORIZADO, CONTROLADO CON PLACEBO DE GRUPOS PARALELOS, MULTICENTRICO, DE FASE IIB/III PARA EVALUAR LA EFICACIA Y SEGURIDAD DE NXY-059 INTRAVENOSO EN ICTUS ISQUEMICO AGUDO.

Datos básicos

Protocolo:
SA-NXY-0006
EUDRACT:
NO ENCUENTRO
NCT:
Centro:
Año de incio:
Año de finalización:
ENSAYO CLÍNICO

Documentos

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Participantes

Financiadores - Promotores

ASTRAZENECA FARMACÉUTICA SPAIN, S.A.

Resultados del Ensayo Clínico


Automatic etiological classification of stroke thrombus digital photographs using a deep learning model

Lucero-Garofano, Alvaro; (...); Manjon, Jose V.

Article. 10.3389/fneur.2025.1534845. 2025

  • Open Access.

Clinical and genetic characteristics of 21 Spanish patients with biallelic pathogenic SPG7 mutations.

Baviera-Muñoz R; (...); Espinós C

Article. 10.1016/j.jns.2021.118062. 2021


Clinical features, mutation spectrum and factors related to reaching molecular diagnosis in a cohort of patients with distal myopathies.

Muelas, Nuria; (...); Vilchez, Juan J

Article. 10.1007/s00415-024-12821-3. 2025


Clot Composition Analysis as a Diagnostic Tool to Gain Insight into Ischemic Stroke Etiology: A Systematic Review

Aliena-Valero, Alicia; (...); Salom, Juan B.

Article. 10.5853/jos.2021.02306. 2021

  • Open Access.

Diagnostic Efficacy of Genetic Studies in a Series of Hereditary Cerebellar Ataxias in Eastern Spain.

Baviera-Munoz, Raquel; (...); Aller, Elena

Article. 10.1212/NXG.0000000000200038. 2022

  • Open Access.

Epidemiology of ataxia and hereditary spastic paraplegia in Spain: A cross-sectional study.

Ortega Suero, G; (...); Sobrido Gomez, M J

Article. 10.1016/j.nrleng.2023.04.003. 2023


Expanding the Clinical Spectrum of DRP2-Associated Charcot-Marie-Tooth Disease.

Sivera R; (...); Sevilla T

Article. 10.1212/WNL.0000000000209174. 2024


Hereditary Spastic Paraplegia 7 Presenting as Multifocal Dystonia with Prominent Cranio-Cervical Involvement

Campins-Romeu, M; (...); Martinez-Torres, I

Letter. 10.1002/mdc3.13257. 2021

  • Open Access.

HIGH CELL-FREE HEMOGLOBIN AND IRON LEVELS IN CLOTS OF COVID-19 STROKE PATIENTS: A NOVEL MECHANISM LINKED TO SARS-COV-2 INDUCED PROTHROMBOTIC STATE

Paya, M.; (...); Segura, T.

Meeting Abstract. 2024


Intra-plaque calcium and its relation with the progression of carotid atheromatous disease.

Miralles, Manuel; (...); Plana, Emma

Article. 10.23736/S0392-9590.22.04872-6. 2022


Late-onset vascular complications of radiotherapy for primary brain tumors: a case-control and cross-sectional analysis.

Ibanez-Julia, Maria-Jose; (...); Ricard, Damien

Article. 10.1007/s11764-023-01350-z. 2023

  • Open Access.

Neurologic complications in herpes simplex encephalitis: clinical, immunological and genetic studies.

Armangue, Thais; (...); Dalmau, Josep

Article. 10.1093/brain/awad238. 2023

  • Open Access.

Proprotein convertase subtilisin/kexin type 9 inhibitors in secondary prevention of vascular events in patients with stroke: Consensus document and practice guidance.

Gil-Núñez A; (...); Palacio E

Practice Guideline. 10.1016/j.nrleng.2020.11.014. 2022

  • Open Access.

Reduced incidence of neurologic complications after allogeneic hematopoietic stem cell transplantation with calcineurin-free graft-versus-host disease prophylaxis.

Balaguer-Rosello, Aitana; (...); Sanz, Jaime

Article. 10.1016/j.jtct.2023.07.008. 2023

  • Open Access.

Reperfusion therapy in acute ischaemic stroke due to cervical and cerebral artery dissection: Results from a Spanish multicentre study.

Campo-Caballero D; (...); Serena J

Article. 10.1016/j.nrleng.2020.10.012. 2023


Role of the nigrosome 1 absence as a biomarker in amyotrophic lateral sclerosis

Isabel Moreno-Gambin, Maria; (...); Vázquez-Costa JF

Article. 10.1007/s00415-021-10729-w. 2021

  • Open Access.

Safety and Efficacy of ApTOLL in Patients With Ischemic Stroke Undergoing Endovascular Treatment: A Phase 1/2 Randomized Clinical Trial.

Hernandez-Jimenez, Macarena; (...); Ribo, Marc

Article. 10.1001/jamaneurol.2023.1660. 2023

  • Open Access.

Spinocerebellar Ataxia 36 is a Frequent Cause of Hereditary Ataxia in Eastern Spain

Baviera-Munoz, Raquel; (...); Bataller, Luis

Article. 10.1002/mdc3.13740. 2023

  • Open Access.

STUB1 Mutations as Possible Genetic Modifiers in Spinocerebellar Ataxia Type 8.

Baviera-Munoz, Raquel; (...); Aller, Elena

Article. 10.1002/mds.29910. 2024

  • Open Access.

The cross-sectional area of the median nerve: An independent prognostic biomarker in amyotrophic lateral sclerosis.

Martinez-Paya, J J; (...); Vazquez-Costa, J F

Article. 10.1016/j.nrleng.2024.07.003. 2024

  • Open Access.

Thymoma and Autoimmune Encephalitis: Clinical Manifestations and Antibodies.

Guasp, Mar; (...); Graus, Francesc

Article. 10.1212/NXI.0000000000001053. 2021

  • Open Access.

Campos de Estudio

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