HPV related diseases represent potential blockbuster markets, but few company’s are currently working on a small-molecule strategy against HPV. This is because:
Broad-spectrum antivirals are not effective against HPV
Existing broad-spectrum antivirals like ribavirine or interferon are not active against HPV-related diseases. Although there is evidence to support a role for the immune system in the hosts defense against the virus, HPV has developed escape mechanisms that make immunomodulation a poor strategy.
No classical drug targets
HPV does not offer any classical drug’able targets, i.e. receptors or enzymes such as polymerases, reverse-transcriptases or proteases. The only viral enzymatic activity (E1 ATPase/helicase) is not specific enough.
No in-vitro assays
The complex biology of the HPV virus has hampered the development of reliable in vitro viral replication systems and reliable animal models. Only a few scientific laboratories around the world have developed animal models for papillomavirus infection, a few others are experts on HPV proteins structure, while even fewer have developed efficient assays to test all the steps of HPV replication.
Anaconda Pharma has developed a unique and proprietary platform for the discovery of small molecules that disrupt E1/E2 interactions. Anaconda Pharma’s unique technology platform includes:
Furthermore, since papillomavirus genomes are not prone to mutation like other viruses (i.e. HIV, influenza), anti-papillomavirus compounds will not be subject to resistance mechanisms and will remain effective with no emergence of resistant strains.
Anaconda Pharma occupies a unique competitive position in the development of anti-HPV therapeutics.
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