Drug intelligence / Profile preview

iPepHANP

Development stage
Preclinical
Lead developer
Emory University
Modality
Peptides, Nanoparticles → Drug Delivery Systems
Administration
Intraperitoneal
01

Overview

iPepHANP is a novel nanotherapeutic consisting of a hyaluronic acid-based nanoparticle (HANP) conjugated to a specific peptide inhibitor (M7) that blocks the interaction between CD154 (CD40 ligand) and CD11b (Mac-1). Developed by researchers at Emory University, iPepHANP is designed to overcome the short in vivo half-life of soluble peptide inhibitors by preventing peptidase-mediated degradation and improving tissue-specific delivery. In preclinical models of transplantation, iPepHANP synergizes with CTLA-4Ig to prolong allograft survival, inhibit donor-reactive CD4+ and CD8+ T cell responses, and promote sustained transplantation tolerance without the need for continuous immunosuppression.

Other names
CD154:CD11b blocking nanoparticleHANP/M7hyaluronic acid nanoparticle-conjugated CD154:CD11b peptide inhibitor
02

Targets

CD40LG (CD40 ligand extracellular domain)

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