Imlunestrant
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(Redirected from LY3484356)
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Other names | LY3484356 |
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Formula | C29H24F4N2O3 |
Molar mass | 524.516 g·mol−1 |
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Imlunestrant is an experimental selective estrogen receptor degrader developed by Eli Lilly and Company for the treatment of some types of breast cancer.[1][2][3]
References
[edit]- ^ Neven, P.; Stahl, N.; Losada, M.J. Vidal; Jimenez, M. Martin; Kaufman, P.A.; Harbeck, N.; Hunt, K.; Carter, S.A.; Bidard, F.C.; Fasching, P.; Aftimos, P.G.; Wheatley, D.; Hamilton, E.P.; Aft, R.; Kulkarni, S.; Ismail-Khan, R.; Karacsonyi, C.; Estrem, S.T.; Ozbek, U.; Ciruelos, E.M. (October 2023). "273P A preoperative window-of-opportunity (WOO) study of imlunestrant in ER+, HER2- early breast cancer (EBC): Final analysis from EMBER-2". Annals of Oncology. 34: S292–S293. doi:10.1016/j.annonc.2023.09.470. S2CID 264385454.
- ^ Jhaveri, Komal; O’Shaughnessy, Joyce; Andre, Fabrice; Goetz, Matthew P.; Harbeck, Nadia; Martín, Miguel; Bidard, Francois-Clement; Thomas, Zachary M.; Young, Suzanne; Ismail-Khan, Roohi; Smyth, Lillian M.; Gnant, Michael (1 March 2023). "Abstract OT1-01-02: EMBER-4: A phase 3 adjuvant trial of imlunestrant vs standard endocrine therapy (ET) in patients with ER+, HER2- early breast cancer (EBC) with an increased risk of recurrence who have previously received 2 to 5 years of adjuvant ET". Cancer Research. 83 (5_Supplement): OT1–01–02-OT1-01–02. doi:10.1158/1538-7445.SABCS22-OT1-01-02.
- ^ Jhaveri, Komal L.; Jeselsohn, Rinath; Lim, Elgene; Hamilton, Erika P.; Yonemori, Kan; Beck, J. Thaddeus; Kaufman, Peter A.; Sammons, Sarah; Bhave, Manali A.; Saura, Cristina; Calvo, Emiliano; Meniawy, Tarek; Larson, Timothy; Ma, Cynthia X.; García-Corbacho, Javier; Cao, Shanshan; Estrem, Shawn T.; Milata, Jennifer L.; Nguyen, Bastien; Beeram, Muralidhar (1 June 2022). "A phase 1a/b trial of imlunestrant (LY3484356), an oral selective estrogen receptor degrader (SERD) in ER-positive (ER+) advanced breast cancer (aBC) and endometrial endometrioid cancer (EEC): Monotherapy results from EMBER". Journal of Clinical Oncology. 40 (16_suppl): 1021. doi:10.1200/JCO.2022.40.16_suppl.1021. S2CID 249445691.