Greetings All,

NanoViricides, Inc. (NYSE: NNVC) is emerging as one of the most exciting small-cap biotech stories heading into 2026. With its lead drug candidate, NV-387, now preparing for Phase 2 human trials, NNVC is redefining the boundaries of antiviral therapy with a bold mission — to deliver the world’s first broad-spectrum antiviral that destroys viruses before they infect cells.

As measles outbreaks sweep the U.S., and the orthopoxvirus family (MPox/Smallpox) resurfaces as a global concern, NV-387 is stepping into the spotlight as a clinically validated, ready-for-action therapy. 

This innovative nanomedicine could become the defining biotech success story of the decade — and Wall Street is beginning to take notice.

The #1 Reason to Watch Now…

According to Zacks Small Cap Research, NanoViricides (NYSE: NNVC) is entering a pivotal valuation phase as it prepares for Phase 2 clinical trials of NV-387. 

The firm has issued a valuation of $7 on NNVC which can be seen HERE.

Zacks analysts highlight that the company’s lead candidate could unlock significant value through multiple commercial pathways — including MPox treatment, U.S. biodefense stockpile procurement for smallpox, and broad respiratory virus indications. 

NNVC’s proven safety data, broad antiviral efficacy in multiple animal models, and advanced regulatory positioning set it apart from typical early-stage peers. 

Financially, the company exited fiscal year 2025 with approximately $1.6 million in cash, later raising an additional $1.25 million through its at-the-market facility to strengthen its runway. 

Zacks emphasizes that positive data from the upcoming MPox Phase 2 trial could rapidly transform NNVC’s valuation profile — positioning the company for strategic partnerships, non-dilutive government funding via BARDA, and potential inclusion in the U.S. Strategic National Stockpile.  

In short, Zacks sees NV-387 as a catalyst capable of redefining NanoViricides’ market potential. 

Crisis Creates Opportunity: The Measles Emergency…

The U.S. faces its most severe measles resurgence in over three decades — with outbreaks expanding across South Carolina, Arizona, Utah, and Nevada. Globally, nations like Canada, Israel, and New Zealand are bracing for renewed epidemics. As vaccination coverage declines, the world needs an immediate therapeutic solution — and NanoViricides’ NV-387 may be that solution.

NV-387’s mechanism is simple yet revolutionary: it binds, traps, and neutralizes viruses in the bloodstream, preventing them from infecting human cells. In preclinical studies, it boosted survival by 130% in measles models while protecting lungs from immune-mediated damage — a major leap in antiviral science!

The Science That Could Redefine Medicine…

Built on TheraCour® nanomedicine technology, NV-387 uses nano-polymer micelles to mimic human cell receptors (heparan-sulfate proteoglycans). When viruses attempt to attach, they instead bind to NV-387, which engulfs and destroys them.

This “decoy-and-destroy” process makes NV-387 resistance-proof, mutation-resistant, and universally effective against a wide range of viruses — from measles and RSV to influenza, COVID-19, MPox, and even smallpox. 

Unlike vaccines or antibody treatments, NV-387 acts independently of the immune system — making it an ideal defense for immunocompromised and high-risk populations.

Phase 2 Trial: Taking Aim at MPox and Beyond…

NNVC is set to launch a Phase 2 clinical trial for MPox in late 2025 or early 2026 in the Democratic Republic of Congo — the epicenter of recent MPox outbreaks.

The upcoming study will evaluate 80 hospitalized patients and compare NV-387 in combination with the standard of care versus standard treatment alone. The trial is already approved by the regional regulatory ethics committee (ACOREP) and backed by a leading Contract Research Organization (CRO).

Positive results could have immediate implications for FDA approval under the Animal Rule for Smallpox, unlocking a $1 billion market via the U.S. Strategic National Stockpile and potential BARDA funding — a major milestone for shareholder value!

Dual-Track Strategy for Maximum Market Impact…

NNVC is executing an aggressive two-track development strategy:

Track 1 – MPox/Smallpox Biodefense Pathway:

The Phase 2 MPox trial could pave the way for U.S. biodefense contracts and inclusion in the Strategic National Stockpile. NV-387’s demonstrated activity against orthopoxviruses positions NNVC as a top candidate for BARDA support — non-dilutive government funding that has historically accelerated major biotech winners.

Track 2 – Empiric Therapy for Respiratory Viruses:

A “basket-type” Phase 2 trial is also planned to evaluate NV-387 as a front-line empiric therapy for multiple viral respiratory infections — a first-of-its-kind approach that mirrors how antibiotics are prescribed. Positive data could establish NV-387 as the world’s first universal antiviral, treating infections before the specific virus is even identified.

Strong Clinical Foundation and Expanding Pipeline…

NV-387 has already cleared Phase 1 safety testing with zero adverse events. Its oral gummies and syrup formulations provide easy patient use, particularly for children and those with severe rashes.

Beyond NV-387, NNVC’s expanding pipeline includes NV-HHV-1 for shingles and preclinical candidates for HIV, Ebola, Rabies, Dengue, and Hepatitis, all based on the same nanoviricide platform. Each represents a potential multi-billion-dollar opportunity in its own right.

The Bottom Line…

NanoViricides, Inc. (NYSE: NNVC) isn’t just another antiviral developer — it’s pioneering a new class of medicine designed to neutralize viruses before infection even begins.  

With Phase 2 trials imminent, BARDA partnerships possible, and orphan drug designations pending, NNVC could soon redefine the antiviral landscape. And with a $7 valuation, the future looks bright. 

NV-387 may very well be the world’s next great antiviral defense — and NanoViricides, Inc. (NYSE: NNVC) could be the top name in biotech to watch in 2026!