Drug intelligence / Profile preview

placebo + pegylated liposomal doxorubicin

Development stage
Unknown
Lead developer
Amgen
Modality
Nanoparticles → Drug Delivery Systems, Small Molecules
Administration
Intravenous
01

Overview

Placebo + PLD is a control arm regimen used in clinical oncology trials, most notably the Phase 3 TRINOVA-2 study (NCT01281254) sponsored by Amgen. This combination consists of an inert placebo administered alongside pegylated liposomal doxorubicin (PLD), which is a liposomal formulation of the anthracycline chemotherapy doxorubicin (marketed as Doxil or Caelyx). The placebo serves as a comparator for an investigational agent (such as trebananib), while PLD provides the standard-of-care chemotherapy backbone. PLD functions by intercalating into DNA and inhibiting topoisomerase II, which disrupts DNA replication and leads to cell death. This regimen is primarily evaluated in patients with recurrent epithelial ovarian, primary peritoneal, or fallopian tube cancers.

Brand names
DoxilCaelyx
Other names
placebo + PLDplacebo plus pegylated liposomal doxorubicinplacebo + Doxilplacebo + Caelyx
02

Targets

TOP2B (DNA topoisomerase II beta)TOP2A (DNA topoisomerase II)

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