Drug intelligence / Profile preview

DP303c + irinotecan liposomes

Development stage
Unknown
Modality
Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Small Molecules, Liposomes → Lipid-based Nanoparticles → Nanoparticles → Drug Delivery Systems
Administration
Intravenous
01

Overview

DP303c + irinotecan liposomes is a **combination drug** under investigation for the treatment of **HER2-expressing gastric adenocarcinoma and gastroesophageal junction adenocarcinoma** in patients who have progressed after one or two prior lines of systemic therapy. **DP303c** is an antibody-drug conjugate (ADC) consisting of an anti-HER2 monoclonal antibody linked to the microtubule inhibitor monomethyl auristatin E (MMAE) via an enzyme-specific linker, enabling targeted cytotoxicity to HER2-positive tumor cells. **Irinotecan liposomes** is a pegylated liposomal formulation of irinotecan, a topoisomerase I inhibitor, providing prolonged circulation and enhanced tumor accumulation through the enhanced permeability and retention (EPR) effect and improved pharmacokinetics compared to conventional irinotecan. The combination leverages the targeted action of the ADC and the DNA-damaging effect of irinotecan to potentially improve efficacy in this cancer subtype[3][7].

02

Targets

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

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