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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorwallace, daniel
dc.contributor.authorGenovese, Mark C
dc.contributor.authorTomic, Davorka Lucia
dc.contributor.authorParsons-Rich, Dana
dc.contributor.authorBolay, Claire Le
dc.contributor.authorMontalban, Xavier
dc.date.accessioned2023-08-02T08:26:23Z
dc.date.available2023-08-02T08:26:23Z
dc.date.issued2023-08
dc.identifier.citationMontalban X, Wallace D, Genovese MC, Tomic D, Parsons-Rich D, Bolay CL, et al. A plain language summary of what clinical studies can tell us about the safety of evobrutinib – a potential treatment for multiple sclerosis. Neurodegener Dis Manag. 2023 Aug;13(4):203–55.
dc.identifier.issn1479-6694
dc.identifier.urihttps://hdl.handle.net/11351/10039
dc.descriptionImmunology; Rheumatology; Systemic lupus erythematosus
dc.description.abstractWhat is this summary about?: This summary explains the findings from a recent investigation that combined the results of over 1000 people from three clinical studies to understand the safety of evobrutinib. Evobrutinib is an oral medication (taken by mouth), being researched as a potential treatment for multiple sclerosis (MS). This medication was also investigated in rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE). Over 1000 people have taken evobrutinib as part of three separate phase 2 clinical studies. These studies looked at how much of the drug should be taken, how safe the drug is, and how well it might work for treating a certain medical condition. What were the results?: Evobrutinib was well-tolerated by participants in all three studies. The number of side effects reported by participants taking the medication was very similar to those reported by participants taking the placebo (a 'dummy' treatment without a real drug). The most common side effects in clinical studies were urinary tract infections, headache, swelling of the nose and throat, diarrhoea and blood markers of potential liver damage (these returned to normal once the treatment was stopped). What do the results mean?: The safety data from all three clinical studies are encouraging and can be used to inform further research into using evobrutinib in MS.
dc.language.isoeng
dc.publisherFuture Medicine
dc.relation.ispartofseriesNeurodegenerative Disease Management;13(4)
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectEsclerosi múltiple - Tractament
dc.subjectProteïnes quinases - Inhibidors - Ús terapèutic
dc.subject.meshMultiple Sclerosis
dc.subject.mesh/drug therapy
dc.subject.meshProtein Kinase Inhibitors
dc.subject.mesh/therapeutic use
dc.titleA plain language summary of what clinical studies can tell us about the safety of evobrutinib – a potential treatment for multiple sclerosis
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.2217/nmt-2023-0003
dc.subject.decsesclerosis múltiple
dc.subject.decs/farmacoterapia
dc.subject.decsinhibidores de proteínas cinasas
dc.subject.decs/uso terapéutico
dc.relation.publishversionhttps://doi.org/10.2217/nmt-2023-0003
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Montalban X] Servei de Neurologia-Neuroimmunologia, Centre d’Esclerosi Múltiple de Catalunya (CEMCAT), Barcelona, Spain. Vall d'Hebron Hospital Universitari, Barcelona, Spain. [Wallace D] Cedars-Sinai Medical Center, David Geffen School of Medicine, University of California, Los Angeles, CA, USA. [Genovese MC] Division of Immunology and Rheumatology, Stanford University, Palo Alto, CA, USA. [Tomic D] Global Clinical Development, Ares Trading SA, Eysins, Switzerland, an affiliate of Merck KGaA. [Parsons-Rich D] Global Clinical Development, EMD Serono Research & Development Institute, Inc., Billerica, MA, USA, an affiliate of Merck KGaA. ECD-Early Clinical Development, Pfizer, Cambridge, Massachusetts, USA. [Bolay CL] Biostatistics, Merck Healthcare KGaA, Darmstadt, Germany
dc.identifier.pmid37345645
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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