AwesomeStocks Donât want emails from us anymore? Click [here]( to unsubscribe. Hello! This is a reminder that our new NYSE alert today is NNVC. NNVC has announced multiple developments over the past few weeks. Yesterday, the company announced: - âCOVID is Here to Stay and NV-387 is a Much Needed Drug Against It, Reminds NanoViricidesâ Here are a couple of the highlights from our profile of NNVC: - NNVC is a previous big winner on multiple occasions.
- We first alerted NNVC earlier this year in May when NNVC was trading under 2.12, it consistently rallied afterwards, reaching a high of 3.59, gains of +69% in a month!
- We alerted it again in June when it was around 1.88, after which over the past month plus it rallied yesterday to a high of 2.55, experiencing gains of +35%! NNVC could present a continued breakout opportunity. Full profile below: New Alert: NanoViricides, Inc. (NYSE American: NNVC) NNVC is a NYSE listed âdevelopment stage company that is creating special purpose nanomaterials for antiviral therapyâ. The Company's ânovel nanoviricide® class of drug candidates are designed to specifically attack enveloped virus particles and to dismantle themâ. NNVCâs âlead drug candidate is NV-387 for the treatment of RSV, COVID-19, Long COVID, Influenza, and other respiratory viral infectionsâ. In addition, the companyâs âother advanced candidate is NV-HHV-1 for the treatment of Shingles (previously referred to as NV-HHV-101)â. As the company further explains: - âNV-CoV-2 (API NV-387) is our nanoviricide drug candidate for COVID-19 that does not encapsulate remdesivir. NV-CoV-2-R is our other drug candidate for COVID-19 that is made up of NV-387 with remdesivir encapsulated within its polymeric micelles.â Importantly: - âThe Company believes that since remdesivir is already US FDA approved, our drug candidate encapsulating remdesivir is likely to be an approvable drug, if safety is comparable. Remdesivir is developed by Gilead. The Company has developed both of its own drug candidates NV-CoV-2 and NV-CoV-2-R independently.â NNVC is also âdeveloping drugs against a number of viral diseases including oral and genital Herpes, viral diseases of the eye including EKC and herpes keratitis, H1N1 swine flu, H5N1 bird flu, seasonal Influenza, HIV, Hepatitis C, Rabies, Dengue fever, and Ebola virus, among othersâ. Importantly: âNanoViricides' platform technology and programs are based on the TheraCour® nanomedicine technology of TheraCour, which TheraCour licenses from AllExcel.â âNanoViricides holds a worldwide exclusive perpetual license to this technology for several drugs with specific targeting mechanisms in perpetuity for the treatment of the following human viral diseases: Human Immunodeficiency Virus (HIV/AIDS), Hepatitis B Virus (HBV), Hepatitis C Virus (HCV), Rabies, Herpes Simplex Virus (HSV-1 and HSV-2), Varicella-Zoster Virus (VZV), Influenza and Asian Bird Flu Virus, Dengue viruses, Japanese Encephalitis virus, West Nile Virus, Ebola/Marburg viruses, and certain Coronaviruses.â Since our last update, in June, the company announced: âOrally Administered NV-387 Results in Ideal Flat Blood Concentration Profile for Sustained Antiviral Effectâ As the company further explained: âThis unusual but highly desirable, extended flat time profile of blood concentration of orally given NV-387 enables sustained antiviral effect over a long period of time, allowing infrequent dosing regimens.â Furthermore: âThe flat time profile of NV-387 indicates that even at very high dosings, its blood concentration is unlikely to result in unwanted side effects. Typical drugs result in a rapid rise in blood concentration of the drug in generally the first hour to a peak, thereafter rapidly exponentially decreasing to baseline in 3-6 hours. In order to ensure that the concentration of the drug is sufficiently high to provide antiviral effect at say 2-4 hours from dosing, the drug dose chosen would be relatively high, and can therefore result in a substantially greater drug concentration in the beginning, which can result in unwanted side effects. Therefore, a sustained, nearly flat drug concentration profile is highly sought-after.â On June 20th, the company announced: âA Novel Broad-Spectrum Antiviral Against Influenza A Viruses, NV-387, Is Effective in Protecting Lungs from Damage in Lethally Infected Animal Modelâ Here are some of the companyâs comments from this press release: "We believe that the lung protection afforded by NV-387 is a very important result. The most severe cases that lead to hospitalization and fatalities in respiratory viral infections involve lung damage as an important factor," said Anil R. Diwan, PhD, President and Executive Chairman of the Company, adding, "This was starkly evidenced during COVID-19 pandemic wherein the Delta variant that caused severe lung damage also caused the largest number of hospitalizations and fatalities. Influenzas, RSV, COVID can all cause severe lung damage resulting in fatalities." As the company further explained: - âNV-387 Treatment Resulted in Significant Reduction in Lung Infiltration and Lung Cell Deathâ
- âNV-387 Treatment Resulted in Significant Reduction in Mucus Load in the Lungsâ
- âNV-387 Treatment Resulted in Significantly Greater Survival Improvement Compared to Three Approved Influenza Drugsâ
- âViral Resistance to NV-387 is Unlikely as Opposed to Known Evolution of Viral Resistance Against Currently Approved Drugsâ
- âNV-387 Has Completed Phase I Human Clinical Trialâ In addition, the company also announced: âA Novel Broad-Spectrum Antiviral Against Influenza A Viruses, NV-387, Could Be an Important Weapon to Fight Bird Flu H5N1, Says NanoViricidesâ As the company further explains: âNanoViricides has recently found that its host-mimetic clinical drug candidate NV-387 was substantially superior to the three approved drugs against influenza, namely Oseltamivir (Tamiflu®, Roche), Peramivir (Rapivab®, Biocryst), and Baloxavir (Xofluza®, Shionogi, Roche) in a lethal animal model study of Influenza A/H3N2 virus lung infection.â Most recently, on July 11, the company announced: âA Single Drug Against Multiple Respiratory Virus Infections - COVID, RSV, Influenza, Bird Flu - Planning Next Phase of Clinical Trials, Says NanoViricidesâ As the company further explains: âNV-387 has completed Phase I clinical trials with no reported adverse events, indicating excellent safety. Closing of the clinical trial site - hospital site itself - is in progress, with different audits taking place to ensure regulatory compliance. Statistical data analysis is expected to begin thereafter. We are eagerly awaiting further information and will provide updates as it becomes available.â âWe have started planning Phase II clinical studies of NV-387 as a treatment for RSV and other indications including Influenza and COVID, as the Phase I clinical trial comes to a close. We plan on taking the drug NV-387 forward on the fastest regulatory path feasible towards regulatory approvals in different countries and jurisdictions including the USA.â In addition, on Wednesday, the company announced: - âCOVID is Here to Stay and NV-387 is a Much Needed Drug Against It, Reminds NanoViricidesâ Make sure to do your own due diligence. Sources: [PR1]( [PR2]( [PR3]( [PR4]( [PR5]( [Website]( [Chart]( Happy Trading! 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