Show simple item record

dc.contributor.authorFisher, Marc
dc.contributor.authorAlbers, Gregory W.
dc.contributor.authorDonnan, Geoffrey A.
dc.contributor.authorFurlan, Anthony J.
dc.contributor.authorGrotta, James
dc.contributor.authorKidwell, Chelsea S.
dc.contributor.authorSacco, Ralph L.
dc.contributor.authorWechsler, Lawrence R.
dc.date2022-08-11T08:09:35.000
dc.date.accessioned2022-08-23T16:36:33Z
dc.date.available2022-08-23T16:36:33Z
dc.date.issued2005-07-16
dc.date.submitted2009-03-31
dc.identifier.citationStroke. 2005 Aug;36(8):1808-13. Epub 2005 Jul 14. <a href="http://dx.doi.org/10.1161/01.STR.0000173403.60553.27">Link to article on publisher's site</a>
dc.identifier.issn1524-4628 (Electronic)
dc.identifier.doi10.1161/01.STR.0000173403.60553.27
dc.identifier.pmid16020764
dc.identifier.urihttp://hdl.handle.net/20.500.14038/38811
dc.description.abstractBACKGROUND: Previous Stroke Therapy Academic Industry Roundtable (STAIR) meetings focused on preclinical evidence of drug efficacy and enhancing acute stroke trial design and performance. A fourth (STAIR-IV) was held to discuss relevant issues related to acute stroke drug development and regulatory approval. SUMMARY OF REVIEW: The STAIR-IV meeting had 3 main focus areas. The first topic was novel approaches to statistical design of acute stroke trials and appropriate outcome measures. The second focus was the need for better cooperation among participants in stroke therapy development that may be addressed through a national consortium of stroke trial centers in the United States and elsewhere. Lastly, regulatory issues related to the approval of novel mono and multiple acute stroke therapies were discussed. CONCLUSIONS: The development of additional acute stroke therapies represents a large unmet need with many remaining challenges and also opportunities to incorporate novel approaches to clinical trial design that will lead to regulatory approval. The STAIR-IV meeting explored new concepts of trial methodology and data analysis, initiatives for implementing a US clinical trialist consortium, and pertinent regulatory issues to expedite approval of novel therapies.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=16020764&dopt=Abstract">Link to Article in PubMed</a>
dc.subjectBrain Ischemia
dc.subjectClinical Trials as Topic
dc.subjectDisease Management
dc.subjectDrug Approval
dc.subject*Health Planning Guidelines
dc.subjectHumans
dc.subjectResearch Design
dc.subjectStroke
dc.subjectThrombolytic Therapy
dc.subjectTreatment Outcome
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleEnhancing the development and approval of acute stroke therapies: Stroke Therapy Academic Industry roundtable
dc.typeJournal Article
dc.source.journaltitleStroke; a journal of cerebral circulation
dc.source.volume36
dc.source.issue8
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=2653&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/1654
dc.identifier.contextkey805475
refterms.dateFOA2022-08-23T16:36:33Z
html.description.abstract<p>BACKGROUND: Previous Stroke Therapy Academic Industry Roundtable (STAIR) meetings focused on preclinical evidence of drug efficacy and enhancing acute stroke trial design and performance. A fourth (STAIR-IV) was held to discuss relevant issues related to acute stroke drug development and regulatory approval. SUMMARY OF REVIEW: The STAIR-IV meeting had 3 main focus areas. The first topic was novel approaches to statistical design of acute stroke trials and appropriate outcome measures. The second focus was the need for better cooperation among participants in stroke therapy development that may be addressed through a national consortium of stroke trial centers in the United States and elsewhere. Lastly, regulatory issues related to the approval of novel mono and multiple acute stroke therapies were discussed. CONCLUSIONS: The development of additional acute stroke therapies represents a large unmet need with many remaining challenges and also opportunities to incorporate novel approaches to clinical trial design that will lead to regulatory approval. The STAIR-IV meeting explored new concepts of trial methodology and data analysis, initiatives for implementing a US clinical trialist consortium, and pertinent regulatory issues to expedite approval of novel therapies.</p>
dc.identifier.submissionpathoapubs/1654
dc.contributor.departmentDepartment of Neurology
dc.contributor.departmentUMass/Memorial Healthcare Center
dc.source.pages1808-13


Files in this item

Thumbnail
Name:
16020764.pdf
Size:
187.0Kb
Format:
PDF

This item appears in the following Collection(s)

Show simple item record