Data from Covalent ERα Antagonist H3B-6545 Demonstrates Encouraging Preclinical Activity in Therapy-Resistant Breast Cancer

Abstract

<div>Abstract<p>Nearly 30% of patients with relapsed breast cancer present activating mutations in estrogen receptor alpha (ERα) that confer partial resistance to existing endocrine-based therapies. We previously reported the development of H3B-5942, a covalent ERα antagonist that engages cysteine-530 (C530) to achieve potency against both wild-type (ERα<sup>WT</sup>) and mutant ERα (ERα<sup>MUT</sup>). Anticipating that the emergence of C530 mutations could promote resistance to H3B-5942, we applied structure-based drug design to improve the potency of the core scaffold to further enhance the antagonistic activity in addition to covalent engagement. This effort led to the development of the clinical candidate H3B-6545, a covalent antagonist that is potent against both ERα<sup>WT/MUT</sup>, and maintains potency even in the context of ERα C530 mutations. H3B-6545 demonstrates significant activity and superiority over standard-of-care fulvestrant across a panel of ERα<sup>WT</sup> and ERα<sup>MUT</sup> palbociclib sensitive and resistant models. In summary, the compelling preclinical activity of H3B-6545 supports its further development for the potential treatment of endocrine therapy–resistant ERα<sup>+</sup> breast cancer harboring wild-type or mutant <i>ESR1</i>, as demonstrated by the ongoing clinical trials (NCT03250676, NCT04568902, NCT04288089).</p>Summary:<p>H3B-6545 is an ERα covalent antagonist that exhibits encouraging preclinical activity against CDK4/6i naïve and resistant ERα<sup>WT</sup> and ERα<sup>MUT</sup> tumors.</p></div>