Drug intelligence / Profile preview

Fv-Hsp72

Development stage
Preclinical
Lead developer
Rubicon Biotechnology
Modality
Fc-Fusion Proteins → Carrier/Scaffold Proteins → Recombinant Proteins and Enzymes
Administration
Intravenous
01

Overview

Fv-Hsp72 is a recombinant fusion protein designed to deliver heat shock protein 72 (Hsp72) directly into damaged or stressed cells. The drug consists of a single-chain variable fragment (Fv) derived from the monoclonal antibody 3E10 fused to human Hsp72. The 3E10-Fv component enables cell penetration by binding extracellular DNA and entering cells via the equilibrative nucleoside transporter 2 (ENT2), which is upregulated in tissues undergoing damage. Once inside the cell, Hsp72 acts as a molecular chaperone that prevents protein misfolding and aggregation, inhibits multiple apoptotic pathways (including Apaf-1 apoptosome formation, AIF-mediated apoptosis, and NF-κB signaling), reduces oxidative stress, and promotes cytoprotection[1][2][4]. Preclinical studies have shown that administration of Fv-HSP72 at reperfusion significantly reduces myocardial apoptosis and improves cardiac function following ischemia-reperfusion injury in animal models[2][3]. It has also demonstrated neuroprotective effects in models of traumatic brain injury by rapidly delivering Hsp72 to prevent secondary cell death[5]. Developed primarily for acute indications such as myocardial infarction and traumatic brain injury, Fv-Hsp72 represents a novel approach for direct intracellular delivery of cytoprotective proteins.

Brand names
Rapid Recovery
Other names
Rapid Recovery drug technology
02

Targets

ex-dsDNA (Extracellular double-stranded DNA)HSPA1A (HSP70-1A)APAF1 (Apoptotic protease-activating factor 1)

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