Drug intelligence / Profile preview

KHK2866 + pegylated liposomal doxorubicin

Development stage
Discontinued
Lead developer
Kyowa Kirin
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules, Nanoparticles → Drug Delivery Systems
Administration
Intravenous
01

Overview

This is a **combination therapy** of **KHK2866**, a recombinant, humanized, non-fucosylated monoclonal antibody targeting **heparin-binding epidermal growth factor-like growth factor (HB-EGF)**, with **pegylated liposomal doxorubicin (PLD)**, an anthracycline chemotherapeutic encapsulated in liposomes and coated with polyethylene glycol. KHK2866 neutralizes HB-EGF activity by preventing its receptor binding, showing tumor-selective distribution. Pegylated liposomal doxorubicin inhibits topoisomerase 2, disrupting DNA replication in cancer cells and is designed for prolonged circulation and targeted tumor delivery. This combination was investigated for advanced cancers, particularly ovarian, fallopian tube, and primary peritoneal cancers[1][3][5].

Other names
PLDPegylated liposomal doxorubicin
02

Targets

DNAHBEGF (Heparin-binding EGF-like growth factor)TOP2A (DNA topoisomerase II)

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