Drug intelligence / Profile preview

sifuvirtide

Development stage
Phase 2
Lead developer
Tianjin FusoGen Pharmaceuticals
Modality
Peptides
Administration
Subcutaneous, Topical
01

Overview

Sifuvirtide is a synthetic 36-amino acid peptide and a potent HIV fusion inhibitor designed to block the entry of HIV into host cells. It acts by binding to the N-terminal heptad repeat (NHR) region of the gp41 transmembrane glycoprotein on the HIV envelope, thereby preventing the conformational changes required for viral and cellular membrane fusion. This mechanism inhibits replication across diverse HIV strains, including those resistant to other fusion inhibitors such as enfuvirtide. Sifuvirtide demonstrates high potency, broad anti-HIV activity against multiple subtypes (A, B, C, B', CRF07_BC, CRF01_AE), low cytotoxicity in vitro, and favorable pharmacokinetic properties. It was rationally designed with engineered salt bridges and hydrogen bonds that enhance its stability and affinity for gp41. The drug has reached phase 2 clinical trials in China for treatment of acquired immunodeficiency syndrome (AIDS)[1][2][4].

Brand names
Sifuvirtide injectionSifuvirtide microbicide
Other names
SFTsifuvirtide
02

Targets

HIV-1 gp41 NHR (HIV-1 gp41 N-terminal heptad repeat region)Viral lipid envelopegp41 (Human immunodeficiency virus type 1 glycoprotein 41)

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