Nanoviricides, Inc 8-K, filed May 21, 2026
Nanoviricides, Inc. (NNVC)
About this 8-K
Nanoviricides, Inc filed this 8-K on May 21, 2026, reporting on events of May 20, 2026.
Items reported
- Item 7.01: Regulation FD disclosure
UNITED STATES
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CURRENT REPORT
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| Item 7.01 | Regulation FD Disclosure. |
NanoViricides, Inc. (the “Company”) participated in the Alliance Global Partners (AGP) Healthcare Companies Showcase held on May 20, 2026. Dr. Anil R. Diwan, PhD, the Company’s President and Executive Chairman, participated as a panelist in a “fireside chat” interview with Dr. James Molloy, Managing Director, Equity Research, A.G.P. Dr. Molloy asked Dr. Diwan a question regarding whether the Company’s drug candidates could help in the current Ebolavirus epidemic in progress in Democratic Republic of Congo (DRC). Dr. Diwan responded as follows:
“During COVID-19, NanoViricides had developed two drug candidates, the first one, NV-387, and a back-up candidate, NV-387 encapsulating Remdesivir. NV-387 is a broad-spectrum antiviral, now entering Phase II clinical trial against Mpox in DRC. Remdesivir had gone into a clinical trial against Ebola already. In that clinical trial, two other antibodies were found to be superior to it and were approved for EBOV Zaire, one was a Regeneron Monoclonal antibodies cocktail, and the other was an antibody isolated and developed from an EBOV-Zaire survivor. Neither of these are responsive for the new Bundibugyo strain in DRC. Efficacy of remdesivir against Ebola in this clinical trial was not established, but safety and tolerability in humans was. That is the basis on which remdesivir entered the very first clinical trials and became the first approved drug to treat COVID-19 patients. Remdesivir was earlier found to be active against Ebola infection in animal models prior to these clinical trials. The problem was that remdesivir metabolizes readily in the bloodstream, limiting its efficacy in humans. Also, remdesivir is an infusion. We therefore developed an oral formulation of remdesivir by encapsulating it inside the NV-387 nanoviricide micelles, and showed that it was active in animal models of COVID. We have also demonstrated that this encapsulation protects remdesivir against bodily metabolism and improves its lifetime and thus its effect. We have in fact published a peer-reviewed paper in PLOS one on these studies. Because NV-387 by itself was highly effective as a broad-spectrum antiviral, we have continued clinical regulatory development of NV-387 by itself. And we keep NV-387 with Remdesivir encapsulated as the back-up candidate. So, to answer your question, yes, we have two candidates, NV-387 itself and NV-387 with Remdesivir encapsulated, both of which are expected to be effective against the current Ebola virus Bundibugyo strain in DRC. In addition, we do have a clinical site in DRC for treatment of Mpox patients. It depends upon the public health responders in DRC how to proceed.”
Some of the above information was previously undisclosed information that could be deduced by persons familiar with the Company based on the Company’s press release dated May 18, 2026, and the Company’s prior work that included Ebola viruses.
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
| NanoViricides, Inc. | ||
| Date: May 21, 2026 | By: | /s/ Anil Diwan |
| Name: | Anil Diwan | |
| Title: | President, Chairman, Chief Executive Officer | |