Log in to save to my catalogue

Comparison of eligibility criteria and baseline characteristics between the patient populations of e...

Comparison of eligibility criteria and baseline characteristics between the patient populations of e...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11713343

Comparison of eligibility criteria and baseline characteristics between the patient populations of evoke and evoke+, Clarity AD, and TRAILBLAZER‐ALZ‐2

About this item

Full title

Comparison of eligibility criteria and baseline characteristics between the patient populations of evoke and evoke+, Clarity AD, and TRAILBLAZER‐ALZ‐2

Publisher

Hoboken: John Wiley and Sons Inc

Journal title

Alzheimer's & dementia, 2024-12, Vol.20 (S6), p.n/a

Language

English

Formats

Publication information

Publisher

Hoboken: John Wiley and Sons Inc

Subjects

Subjects and topics

More information

Scope and Contents

Contents

Background
evoke and evoke+ are phase 3, randomized, placebo‐controlled trials currently investigating the glucagon‐like peptide‐1 receptor agonist semaglutide as disease‐modifying therapy (DMT) in persons with early Alzheimer’s disease (AD). How the evoke and evoke+ trial populations compare with other phase 3 programs for DMTs in early AD has...

Alternative Titles

Full title

Comparison of eligibility criteria and baseline characteristics between the patient populations of evoke and evoke+, Clarity AD, and TRAILBLAZER‐ALZ‐2

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11713343

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11713343

Other Identifiers

ISSN

1552-5260

E-ISSN

1552-5279

DOI

10.1002/alz.083684

How to access this item