作者
Jun Liang,Jason R. Zbieg,Robert A. Blake,Jae H. Chang,Stephen Daly,Antonio G. DiPasquale,Lori S. Friedman,Thomas Gelzleichter,Matthew Gill,Jennifer M. Giltnane,Simon Goodacre,Jane Guan,Steven J. Hartman,Ellen Ingalla,Lorn Kategaya,James R. Kiefer,Tracy Kleinheinz,Sharada S. Labadie,Tommy Lai,Jun Li,Jiangpeng Liao,Zhiguo Liu,Vidhi Mody,Neville McLean,Ciara Metcalfe,Michelle Nannini,Jason Oeh,Martin O’Rourke,Daniel F. Ortwine,Yingqing Ran,Nicholas C. Ray,Fabien Roussel,Amy Sambrone,Deepak Sampath,Leah Schutt,Maia Vinogradova,John S. Wai,Tao Wang,Ingrid E. Wertz,Jonathan White,Siew Kuen Yeap,Amy Young,Birong Zhang,Xiaoping Zheng,Wei Zhou,Yu Zhong,Xiaojing Wang
摘要
Breast cancer remains a leading cause of cancer death in women, representing a significant unmet medical need. Here, we disclose our discovery efforts culminating in a clinical candidate, 35 (GDC-9545 or giredestrant). 35 is an efficient and potent selective estrogen receptor degrader (SERD) and a full antagonist, which translates into better antiproliferation activity than known SERDs (1, 6, 7, and 9) across multiple cell lines. Fine-tuning the physiochemical properties enabled once daily oral dosing of 35 in preclinical species and humans. 35 exhibits low drug-drug interaction liability and demonstrates excellent in vitro and in vivo safety profiles. At low doses, 35 induces tumor regressions either as a single agent or in combination with a CDK4/6 inhibitor in an ESR1Y537S mutant PDX or a wild-type ERα tumor model. Currently, 35 is being evaluated in Phase III clinical trials.