Drug intelligence / Profile preview

trastuzumab deruxtecan + azenosertib

Development stage
Unknown
Lead developer
Zentalis Pharmaceuticals
Modality
Small Molecules, Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous, Oral
01

Overview

**Trastuzumab deruxtecan + azenosertib** is an investigational combination therapy pairing trastuzumab deruxtecan (T-DXd, Enhertu), an antibody-drug conjugate (ADC) developed by Daiichi Sankyo and AstraZeneca, with azenosertib (ZN-c3), an oral small molecule WEE1 kinase inhibitor from Zentalis Pharmaceuticals (now with GSK involvement). T-DXd targets **HER2** (human epidermal growth factor receptor 2) via a humanized monoclonal antibody conjugated to a topoisomerase I inhibitor payload (deruxtecan) through a cleavable tetrapeptide-based linker, enabling selective delivery and DNA damage in HER2-expressing tumor cells. Azenosertib selectively inhibits **WEE1** (serine/threonine-protein kinase WEE1), abrogating the G2/M DNA damage checkpoint to sensitize cancer cells to DNA-damaging agents like the T-DXd payload, promoting replication stress and apoptosis. This synergy is being evaluated in a Phase 1 dose-escalation/expansion trial (NCT06364410) for **HER2-expressing/amplified solid tumors**, including gastric/gastroesophageal junction adenocarcinoma and others that are locally advanced, metastatic, or unresectable.[1][4][5]

Brand names
Enhertu + azenosertib
02

Targets

TOP1 (DNA Topoisomerase I)WEE1 (WEE1 G2 checkpoint kinase)ERBB2 (Erb-b2 receptor tyrosine kinase 2)

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