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AdCMVp53

Development stage
Phase 3
Lead developer
UT Southwestern Medical Center
Modality
Gene Silencing → Gene Therapies, Adenoviral Vectors → Other Viral Vectors → Viral Vectors → Gene Addition/Replacement → Gene Therapies, Gene Editing → Gene Therapies
Administration
Intratumoral, Intraperitoneal
01

Overview

AdCMVp53 is an adenoviral vector-based gene therapy encoding wild-type human p53 under control of the cytomegalovirus (CMV) promoter. It is designed for direct delivery of functional p53 into tumor cells lacking effective p53, thereby inducing cell cycle arrest or apoptosis. This agent has been investigated primarily for the treatment of cancers with p53 mutation, including ovarian cancer[2], head and neck squamous cell carcinoma, hepatocellular carcinoma, lung cancer, and others. Restoring p53 function aims to suppress tumor growth, enhance chemosensitivity, and overcome resistance to conventional therapies[1][2][3][5].

Other names
AdCMVp53AdCMVp-53AdCMVp 53Ad-CMV-p53Ad-CMV-p-53Ad-CMV-p 53adenovirus-based p53 gene therapyadenoviral vector p53
02

Targets

TP53 (Cellular Tumor Antigen p53 R175H)

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