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liposome entrapped docetaxel

Development stage
Phase 2
Lead developer
Neopharm
Modality
Small Molecules, Liposomes → Lipid-based Nanoparticles → Nanoparticles → Drug Delivery Systems
Administration
Intravenous
01

Overview

Liposome entrapped docetaxel (LE-DT) is a formulation of the chemotherapeutic agent docetaxel encapsulated within liposomes. This approach aims to improve the solubility and pharmacokinetics of docetaxel while reducing toxicity associated with conventional formulations that use solvents like Tween 80. Liposomal encapsulation can provide sustained drug release, protection from degradation and toxicities, and may help overcome multidrug resistance. Preclinical studies have shown improved anti-tumor effects and reduced toxicity compared to free docetaxel. Clinical trials in patients with advanced solid tumors demonstrated that LE-DT is generally well tolerated with expected toxicities such as neutropenia but less neuropathy or edema than standard formulations. The mechanism of action remains inhibition of tubulin polymerization leading to cell cycle arrest[2][4][5][6][7].

Other names
liposomal docetaxeldocetaxel liposomalliposome-encapsulated docetaxelDTX-liposomeDocetaxel injection concentrate for nanodispersionDocetaxel nanodispersion
02

Targets

BCL-2 (BCL-2 family)TUBB (Tubulin (alpha and beta subunits))

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