Other agents are under investigation for their ability to interact with the proteins involved in HIV entry and the possibility that they may serve as entry inhibitors. •
Leronlimab, a monoclonal antibody that binds CCR5 •
Plerixafor was being developed to interfere with interaction between HIV and CXCR4, but showed little useful antiviral activity in recent trials. •
Epigallocatechin gallate, a substance found in
green tea, appears to interact with
gp120 as do several other
theaflavins. •
Vicriviroc, similar to maraviroc, is currently undergoing clinical trials for FDA approval. •
Aplaviroc, an agent similar to maraviroc and vicriroc. Clinical trials were halted in 2005 over concerns about the drug's safety. • b12 is an
antibody against HIV found in some
long-term nonprogressors. It has been found to bind to
gp120 at the exact region, or
epitope, where
gp120 binds to CD4. b12 seems to serve as a natural entry inhibitor in some individuals. It is hoped that further study of b12 may lead to an effective HIV vaccine. •
Griffithsin, a substance derived from algae, appears to have entry inhibitor properties. •
DCM205, is a small molecule based on L-
chicoric acid, an integrase inhibitor. DCM205 has been reported to inactivate HIV-1 particles directly
in vitro and is thought to act primarily as an entry inhibitor. • CD4 specific Designed
Ankyrin Repeat Proteins (
DARPins) potently block viral entry of diverse strains and are being developed and studied as potential microbicide candidates • A polyclonal
caprine antibody is in phase II human
clinical trials that targets, among others sites, the GP41 transmembrane glycoprotein. The trials are being conducted by Virionyx, a New Zealand Company. •
VIR-576 is a synthesized peptide which binds to gp41, preventing fusion of the virus with a cell membrane. • ITX5061 for
hepatitis C. == References ==