Elacestrant: a new FDA-approved SERD for the treatment of breast cancer

dc.contributor.authorBhatia, Neha
dc.contributor.authorThareja, Suresh
dc.date.accessioned2024-01-21T10:38:34Z
dc.date.accessioned2024-08-13T12:05:31Z
dc.date.available2024-01-21T10:38:34Z
dc.date.available2024-08-13T12:05:31Z
dc.date.issued2023-05-16T00:00:00
dc.description.abstractElacestrant (RAD-1901), a selective estrogen receptor degrader, was approved by USFDA on January 27, 2023, for the treatment of breast cancer. It has been developed by Menarini Group under the brand name Orserdu�. Elacestrant showed anticancer activity both in vitro and in vivo in ER+ HER2-positive breast cancer models. The present review delebrates the development stages of Elacestrant, with its medicinal chemistry, synthesis, mechanism of action, and pharmacokinetic studies. Clinical data and safety profile has also been discussed, including data from randomized trials. � 2023, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.en_US
dc.identifier.doi10.1007/s12032-023-02045-2
dc.identifier.issn13570560
dc.identifier.urihttps://kr.cup.edu.in/handle/32116/3605
dc.identifier.urlhttps://link.springer.com/10.1007/s12032-023-02045-2
dc.language.isoen_USen_US
dc.publisherSpringeren_US
dc.subjectBreast canceren_US
dc.subjectElacestranten_US
dc.subjectEstrogenen_US
dc.subjectOrserduen_US
dc.subjectSERDen_US
dc.titleElacestrant: a new FDA-approved SERD for the treatment of breast canceren_US
dc.title.journalMedical Oncologyen_US
dc.typeReviewen_US
dc.type.accesstypeClosed Accessen_US

Files