Drug intelligence / Profile preview

liposomal curcumin (Medical University of Vienna)

Development stage
Unknown
Lead developer
Medical University of Vienna
Modality
Small Molecules, Lipid-based Nanoparticles → Nanoparticles → Drug Delivery Systems
Administration
Intravenous
01

Overview

Lipcor (liposomal curcumin) is an investigational liposomal formulation of the natural polyphenol curcumin, specifically developed for the treatment of rare and aggressive pediatric central nervous system (CNS) tumors. Developed in collaboration with the Medical University of Vienna, the formulation is currently being evaluated in clinical trials (such as the LIPCOR study) for patients with recurrent or refractory medulloblastoma, ependymoma, and atypical teratoid rhabdoid tumors (ATRT). Curcumin is known for its potent anti-neoplastic, anti-inflammatory, and antioxidant properties; however, its clinical utility is typically limited by poor aqueous solubility and low systemic bioavailability. The liposomal delivery system in Lipcor is designed to enhance the stability and pharmacokinetic profile of curcumin, potentially improving its ability to cross the blood-brain barrier. Mechanistically, curcumin acts as a pleiotropic inhibitor of multiple oncogenic signaling pathways, including NF-κB, STAT3, and Wnt/β-catenin, thereby inducing apoptosis and inhibiting tumor cell proliferation and survival.

Other names
curcumin liposomal
02

Targets

AKT1 (Proto-oncogene serine/threonine-protein kinase Akt1)CTNNB1 (Beta-catenin)NF-κBPI3K (Phosphoinositide-3-kinase regulatory subunit 6)STAT3 (Signal Transducer and Activator of Transcription 3)

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