Drug intelligence / Profile preview

oAd + LP

Development stage
Preclinical
Lead developer
GeneMedicine
Modality
Viral-delivered RNAi → In Vivo RNAi → Gene Silencing → Gene Therapies, Oncolytic Viruses → Oncolytic Therapeutics, Lipid-based Nanoparticles → Nanoparticles → Drug Delivery Systems
Administration
Intravenous
01

Overview

oAd + LP is an experimental therapeutic formulation consisting of an oncolytic adenovirus (oAd) encapsulated within a lipid envelope (liposome). In the specific research context provided, the oAd is engineered to co-express short-hairpin RNA (shRNA) against Wnt5 (shWnt5) and the proteoglycan decorin to enhance antitumor efficacy. The liposomal encapsulation (LP) is designed to protect the viral particles from systemic clearance and reduce non-specific accumulation in the liver, which are common limitations of systemic oncolytic virotherapy. While this formulation lacks the advanced pH-responsive and EGFR-targeting modifications of related variants (such as oAd/LP-GE-PS), it serves as a foundational delivery system that demonstrates improved safety profiles and attenuated hepatic toxicity compared to naked adenovirus in preclinical models of EGFR-positive breast cancer.

Other names
liposomal oncolytic adenovirusliposome-encapsulated oncolytic adenovirus
02

Targets

DCN (Decorin)VLDL (Very low-density lipoprotein)WNT5A (Protein Wnt-5a)

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