and have Priority Review for their supplemental Biologics License Application (sBLA) from the US Food and Drug Administration (FDA) of antibody-drug conjugate (ADC), Enhertu (trastuzumab deruxtecan), to treat unresectable or metastatic HER2-low breast cancer in adults.

The treatment is intended for HER2-low immunohistochemistry [IHC] 1+ or IHC 2+/in-situ hybridisation [ISH]-negative breast cancer patients who have previously received treatment in the metastatic setting. 

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Being co-developed and co-marketed by , along with , Enhertu is a HER2-directed ADC.

An action date for the decision from the regulatory agency or the Prescription Drug User Fee Act date on the therapy is expected in the fourth quarter of this year.

The application is being analysed under the Real-Time Oncology Review (RTOR) programme and Project Orbis, two FDA initiatives to rapidly make available effective therapies for cancer.

AstraZeneca noted that the sBLA is based on findings from the randomised, open-label Phase III DESTINY-Breast04 clinical trial of Enhertu in priorly treated subjects with HER2-low metastatic breast cancer with hormone receptor (HR)-positive or HR-negative disease. 

According to the findings, the ADC offered clinically meaningful efficacy in progression-free survival (PFS) and overall survival (OS) in trial subjects compared to standard of care chemotherapy of physician鈥檚 choice.

Furthermore, Enhertu鈥檚 safety profile was in line with prior trials without any new safety concerns reported. 

AstraZeneca Oncology R&D executive vice-president Susan Galbraith said: 鈥淭he data from DESTINY-Breast04 represent the first time a HER2-targeted therapy has shown a survival benefit in patients with HER2-low metastatic breast cancer. 

鈥淚f approved, Enhertu will redefine how we classify and treat metastatic breast cancer, enabling patients whose tumours have lower levels of HER2 expression the opportunity to benefit from a HER2-directed therapy.鈥�

In January, the FDA granted priority review for Enhertu to treat adults with unresectable or metastatic HER2-positive breast cancer who have previously received an anti-HER2-based regimen.