Drug intelligence / Profile preview

camizestrant + atirmociclib

Development stage
Unknown
Lead developer
AstraZeneca
Modality
Small Molecules
Administration
Oral
01

Overview

Camizestrant + atirmociclib is an investigational combination therapy developed by AstraZeneca for the treatment of estrogen receptor-positive (ER+), human epidermal growth factor receptor 2-negative (HER2-) advanced breast cancer. Camizestrant (AZD9833) is a next-generation, potent, oral selective estrogen receptor degrader (SERD) that functions by binding to, antagonizing, and inducing the degradation of the estrogen receptor alpha (ERα), including common ESR1 mutations. Atirmociclib (AZD9829) is a highly selective cyclin-dependent kinase 4 (CDK4) inhibitor. By specifically targeting CDK4 over CDK6, atirmociclib aims to reduce the hematological toxicities, such as neutropenia, typically associated with dual CDK4/6 inhibitors while maintaining efficacy in inhibiting cell cycle progression. This combination is being evaluated in clinical trials, such as SERENA-1b, to improve outcomes for patients who have previously received CDK4/6 inhibitor therapy.

Other names
AZD9833 + AZD9829
02

Targets

CDK4 (Cyclin-dependent kinase 4)ESR1 (ERα)

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