NanoViricides (NYSE American: NNVC), a global leader in broad-spectrum antiviral nanomedicines, is reporting that, in a lethal animal model, its lead drug candidate, NV-387, showed ultra-broad antiviral activity, including activity against the orthopoxvirus family, including smallpox and mpox. According to the announcement, in the model of lung infection by Ectromelia virus, oral dosing with NV-387 showed an increase in lifespan of mice comparable to oral treatment with tecovirimat (TPOXX[R], SIGA), which is currently the approved drug against smallpox.
“We have completed a lethality animal study wherein animals were infected with ectromelia virus into the lungs directly,” stated the company in the press release. “In this study, we found that NV-387 alone treated animals survived 15 days, tecovirimat alone treated animals survived 16 days, and NV-387 plus tecovirimat treated animals survived 19 days, whereas vehicle-treated animals died in 8 days. Therefore, we believe that NV-387 is a viable clinical candidate to be developed by itself for the treatment of poxvirus infections under the US FDA ‘Animal Rule.’ In addition, we believe that the combination of NV-387 and tecovirimat could reduce the potential for escape resistant generation against tecovirimat, as is known with other drug combination studies against viruses.”
To view the full press release, visit https://ibn.fm/BMZGa
About NanoViricides Inc.
NanoViricides is a development-stage company that is creating special purpose nanomaterials for antiviral therapy. The company’s lead drug candidate is NV-387 for the treatment of RSV, COVID-19, Long COVID and other respiratory viral infections. Its other advanced candidate is NV-HHV-1 for the treatment of shingles rash, HSV-1 “cold sores” and HSV-2 “genital ulcers.” The company cannot project an exact date for filing an IND for any of its drugs because of dependence on a number of external collaborators and consultants. To learn more about the company, visit www.NanoViricides.com.
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