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NanoViricides Reports Breakthrough in Treating Airborne Viruses, Boosting Lifespan in Infected Mice

NanoViricides Reports Breakthrough in Treating Airborne Viruses, Boosting Lifespan in Infected Mice

NanoViricides報告在治療空氣傳播病毒方面取得突破,可延長受感染小鼠的壽命
Benzinga ·  05/08 18:37

NanoViricides, Inc. (NYSE:NNVC) (the "Company"), a global leader in broad-spectrum antiviral nanomedicines, says that the ultra-broad antiviral activity spectrum of NV-387 includes activity against orthopoxvirus family (Smallpox/Mpox), with both inhalation and skin abrasion (sexual) modes of infection acquisition. Ectromelia virus infection of mice is a model for Smallpox infection in humans, and also serves as a surrogate for MPox infection in humans. All three viruses belong to the orthopoxvirus family.

廣譜抗病毒納米藥物領域的全球領導者Nanoviricides, Inc.(紐約證券交易所代碼:NNVC)(“公司”)表示,NV-387 的超寬抗病毒活性譜包括對正痘病毒家族(天花/Mpox)的活性,包括吸入和皮膚磨損(性)感染獲取方式。小鼠的Ectromelia病毒感染是人類天花感染的模型,也是人類mPOx感染的替代品。所有三種病毒都屬於正交病毒家族。

NanoViricides reports that in a lethal animal model of lung infection by Ectromelia virus, oral dosing with NV-387 led to an increase in lifespan of mice that was comparable to oral treatment with tecovirimat (TPOXX, SIGA), the approved drug against Smallpox.

NanoViricides報告說,在Ectromelia病毒肺部感染的致命動物模型中,口服 NV-387 可以延長小鼠的壽命,這與經批准的抗天花葯物tecovirimat(TPOXX,SIGA)的口服治療相當。

This lung infection study substantiates the results of the previously reported intradigital footpad infection study that: (i) NV-387 has comparable antiviral activity as tecovirimat, and
(ii) NV-387 plus tecovirimat has much stronger antiviral activity than either drug alone.

這項肺部感染研究證實了先前報告的數字腳墊感染研究的結果,即:(i)NV-387 具有與 tecovirimat 相當的抗病毒活性,以及
(ii) NV-387 和 tecovirimat 的抗病毒活性比單獨使用任何一種藥物都強得多。

We have completed a lethality animal study wherein animals were infected with ectromelia virus into the lungs directly. 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.

我們已經完成了一項致死性動物研究,在該研究中,動物被直接感染到肺部的 ectromelia 病毒。在這項研究中,我們發現單獨治療 NV-387 的動物存活了 15 天,單獨治療 tecovirimat 的動物存活了 16 天,經過 NV-387 和 tecovirimat 治療的動物存活了 19 天,而經過載體治療的動物在 8 天內死亡。

This lung-infection study emulates infection from aerosolized dispersion of the virus, as may be expected in a bioterrorism scenario.

這項肺部感染研究模擬了病毒氣溶膠傳播引起的感染,這在生物恐怖主義情景中是可以預料的。

譯文內容由第三人軟體翻譯。


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