IHC analysis of paired biopsies at screening and cycle 1 day 15 showed a trend toward dose-dependent ER degradation for single-agent LSZ102 ( Fig. 2B ), which did not appear to be affected by ribociclib or alpelisib (Supplementary Fig.
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A Phase I Study of LSZ102, an Oral Selective Estrogen Receptor Degrader, with or without Ribociclib or Alpelisib, in Patients with Estrogen Receptor-Positive Breast Cancer.
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Degradation of ER was observed in all treatment arms, with an apparent trend suggesting an LSZ102 dose response.