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Hello!
New Alert: NanoViricides, Inc. (NYSE American: NNVC)
NNVC is our new NYSE American biotech alert.
NNVC is trading under 2.00 - and it is advancing what could be one of the most timely drug candidates in the biotech space today.
NNVC has delivered multiple big wins in the past, with previous breakouts reaching gains of +35%, +53%, +44% & +25%!
Following our previous alert in May, NNVC rallied upwards of +55%!
Now, NNVC could be positioning for its next move higher.
NNVC is a NYSE American listed “clinical stage company that is creating special purpose nanomaterials for antiviral therapy”.
NNVC is a “leading global pioneer in the development of broad-spectrum antivirals based on host-mimetic nanomedicine technology that viruses cannot escape”.
Most antiviral drugs work by attacking a specific part of a specific virus.
The problem: viruses mutate. And when they do, the drug stops working.
NNVC took a fundamentally different approach.
NNVC’s “lead drug candidate is NV-387, a broad-spectrum antiviral drug that we plan to develop as a treatment of RSV, COVID, Long COVID, Influenza, and other respiratory viral infections, as well as MPOX/Smallpox infections, and even Measles.”
“NV-387 is a revolutionary antiviral that we believe will be the drug offered at “ first visit” when the patient presents to a doctor with any respiratory viral illness.”
Viruses cannot escape NV-387 because no matter how much a virus changes, it continues to bind to the sulfated proteoglycan attachment receptor(s) of the host which the virus needs to cause infection as well as for human-to-human transmission.
NV-387 mimics the critical features of the conserved attachment receptors on the host-side that over 90% of viruses are known to use.
This escape-resistant drug feature of NV-387 solves the biggest problem in antiviral medical countermeasures: Viruses readily evolve to escape the countermeasures in the field, whether vaccines, antibodies, or traditional small chemical drugs.
NV-387 has an extremely broad spectrum of antiviral activity.
“To date, it has been found to be highly active against every virus that we have tested in animal models:
NV-387 treatment was found to be able to cure lethal RSV infection in mice.
NV-387 treatment was substantially superior to the existing treatments, namely Tamiflu (oseltamivir) and Xofluza (baloxavir) in a lethal infection with H3N2 Influenza A virus.
NV-387 treatment was highly effective in an animal model for MPox using dermal orthopoxvirus infection.
NV-387 treatment was highly effective in an animal model for Smallpox using lethal lung infection with orthopoxvirus.
In addition, NV-387 treatment was highly effective in a humanized animal model (hSLAM+k.i., InfAR-/- mice) in lethal infection with Measles virus.
Thus, NV-387, as a single drug, is responding to several unmet medical needs in viral infectious diseases at once.”
The company has “filed "Orphan Drug Designation" (ODD) applications with the US FDA for three different scenarios, namely:
NV-387 for the treatment of Measles,
NV-387 for the treatment of MPox, and
NV-387 for the treatment of Smallpox.”
“Orphan drug designation, if approved, will provide us with several incentives.”
“These include frequent communication with the FDA, an additional 7 years of market exclusivity, certain R&D tax benefits, and waiver of certain FDA PDUFA fees.”
“These incentives are expected to result in a shorter timeline of the regulatory process as compared to NV-387 development for Influenza or RSV.”
Sadly, at present:
“There is no approved drug for Measles.
There is no approved drug for MPox.
The Smallpox approved drugs (under FDA Animal Rule) have significant shortcomings, leaving the US practically unprepared for this bioterrorism scenario despite several billions of dollars in development and acquisitions.”
NNVC also “applied for a "Rare Pediatric Disease Drug" (RPDD) designation for NV-387 for the treatment of Measles.”
As the company further explains:
“If granted, the RRPD will enable us to obtain a Priority Review Voucher (PRV) upon drug approval from the FDA, which is a tradable instrument. Recently, a PRV was sold for $180 million.”
“This would represent a revenue-generation opportunity even prior to commercial market sales of the drug.”
The commercial opportunity the company is targeting is substantial.
“The overall market size of NV-387 indications is estimated to be well in excess of $10 billion.”
“NV-387 is designed to shape-shift upon binding to the virus particle, in the process disrupting the virus particle and making it incapable of infection, as a complete chemical nanomachine that destroys the virus”.
“The revolutionary broad antiviral spectrum of NV-387 is reminiscent of the dawn of antibiotics to combat bacterial infections.”
Importantly:
“NV-387 is expected to become an "emperic therapy" for viral infections, just as antibiotics such as amoxicillin are used as emperic therapies for bacterial infections.”
“NV-387 would be the first ever drug enabling emperic antiviral therapy, and would be potentially as revolutionary to antiviral therapy as antibiotics have been to anti-bacterial therapy.”
Emperic therapy means when the patient presents to the doctor, immediately the antiviral drug can be prescribed and started without having to wait for discriminating test results as to which virus is causing the infection.
This has “tremendous benefits since antiviral drugs are most effective when given as early as possible upon viral infection”.
“NanoViricide Platform Enables Drug Rescue, Oral Drug Delivery, and Zip-Code Specific Delivery”:
“Oral drug delivery of small chemicals, peptides (such as the GLP-a obesity drugs), and proteins is feasible by encapsulation of the guest drug into the nanoviricide polymeric micelle. The encapsulation protects the guest from metabolism thereby enabling effective drug delivery.”
“Encapsulation of a difficult or failed drug within the nanoviricide polymeric micelle can enable rescue of the drug candidate turning it into a clinically viable drug candidate, saving hundreds of millions of dollars of development work.”
“Going another step further, the nanoviricide platform technology can be customized to enable zip-code-like specific delivery of encapsulated drugs to specific tissues (e.g. non-liver targeted delivery),, cells (e.g. cancer-cell specific delivery sparing normal cells), bacteria, or viruses (e.g. NV-HHV-1, NV-HIV-1) in a fully synthetic chemistry based, scalable technology stack.”
The company has announced multiple developments over the past month.
On May 4, 2026, the company announced:
“NV-387 for The Treatment of Measles is Granted Orphan Drug Designation by The US FDA”
Here are the company’s comments from this press release:
"The Orphan Drug Designation is an important milestone that will help us speed up the regulatory development of NV-387 for the Treatment of Measles," said Anil R. Diwan, PhD., adding, "NV-387, as an effective drug would be an important tool to fight Measles resurgence in the USA and worldwide, when approved."
Importantly:
“NV-387 is the only drug candidate to our knowledge that has demonstrated strong in vivo activity against lethal infection with the Measles virus in a humanized animal model study.”
Sadly:
“Measles cases have been rising globally. This year, a major epidemic has broken out in Bangladesh with over 227 children dead and over 35,000 cases, while Guatemala has an on-going Measles outbreak with over 5,300 cases and four deaths[2].”
“Measles cases are rising across the Western world including several European countries and the UK, as well as the USA and Canada. Additionally Mexico and several other Central and South American countries have also been suffering from rising Measles outbreaks.
Measles is endemic globally. Many countries that had achieved an elimination status for Measles have by now lost this status, due to severe outbreaks over the last three years[3].
Measles cases have been rising in the USA. As of April 30, 2026, already 1,803 confirmed measles cases (excluding 11 in international travelers) were reported in the United States in 2026. in the year 2025, 2,251 confirmed cases with 3 deaths were reported, increasing from 285 in 2024 and 59 in 2023 (no deaths in these prior years). Vaccine breakthrough accounted for 6-7% of cases, with the remaining cases being in unvaccinated or persons with unknown vaccine status. (CDC data[4]).
Measles continues to be a rare disease in the USA, with annual incidence rates well below 200,000 cases, which has qualified NV-387 for Measles Treatment as an Orphan Drug indication.”
In addition, the company also announced:
“Recent Hantavirus On A Cruise Ship Highlights the Need for Broad-Spectrum Antiviral Drugs Such as NV-387, Says NanoViricides”
Here are some of the company’s comments from this press release:
"NV-387 could have possibly saved lives of the infected patients, given the preponderance of evidence on effectiveness of NV-387 in lethal lung infections in animal models," said Anil R. Diwan, PhD, President and Executive Chairman of the Company, adding, "Physicians in charge could have sought it under emergency or expanded use procedures, given that there is no drug for the treatment of hantavirus infections. NV-387 has successfully completed Phase I clinical trial of safety and tolerability in healthy human volunteers."
Importantly:
“NanoViricides, Inc. has used exactly this route of infection in our lethal animal models of many distinctly different viruses for testing NV-387. We have found NV-387 to be highly effective in treating every one of the viruses that we have tried so far, including: Coronaviruses, RSV, Influenza, Monkeypox, and even Measles virus.”
“The economic cost of the global effort for this single incidence is tremendous, not to mention the inconveniences to all involved, including the passengers, their contacts, health care workers, and all persons who were brought in to control this situation so that it does not explode into a global outbreak.”
In addition, the company announced:
“Ebola Global Health Emergency Needs a Broad-Spectrum Drug - NV-387 is a Strong Potential Candidate, Says NanoViricides”
As the company further explains:
“Viruses are unlikely to escape NV-387 because no matter how much the viruses change, they still depend upon their interaction with sulfated proteoglycans for initial attachment to cells, which NV-387 mimics.”
“In contrast, antibodies and vaccines are highly specific, and are readily escaped by viruses. Further, antibodies require a cold chain and must be given as infusions in patients. The equipment and facilities for the cold chain and for infusion itself in a high isolation setting are generally not available in remote areas.”
In addition, the company also announced:
“NanoViricides, Inc. Has Filed its Quarterly Report - NV-387 Advancing for Phase II”
“NanoViricides Announces Closing of ~$2 Million Registered Direct Offering”
Most recently, last week, the company announced:
“In the Ebola Emergency, NV-387 is Ready to be Shipped to DRC, and It Compares Favorably as a Treatment for Ebola Versus Possible Options, Says NanoViricides”
As the company further explains:
“The rare Bundibugyo strain of Ebola virus causing the current outbreak appears to be its new variant, likely freshly introduced from some animal source[1], such as fruit bats.”
“The outbreak which was declared a public health emergency of international concern by the WHO on May 16, 2026, is rapidly expanding, outpacing containment efforts, with over 900 suspected cases and over 220 deaths, in a high traffic region bordering the Democratic Republic of Congo (DRC), Uganda, and South Sudan and with 11 more nations in Africa at risk[2].”
“There are no approved vaccines or treatments against the Bundibugyo virus.”
Here are some of the company’s comments from this press release:
"We believe NV-387 could be effective against the Bundibugyo strain of Ebola that is spreading rapidly in Africa," said Anil R. Diwan, PhD, adding, "All filoviruses including all Ebola strains utilize the sulfated proteoglycans for initial cell attachment; which is the feature that NV-387 presents to the viruses to destroy them."
NNVC could be positioned to breakout higher.
Make sure to do your own due diligence.
Happy Trading!
SmallCapStocks Team
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