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Hello!
Following our alert this morning, NNVC opened at 1.40 and rallied to a high of 1.56, a gain of +11%.
In October, NNVC rallied +44% following our last alert, reaching a high of 2.23.
That is +59% from today’s open.
Here are a couple of the things to keep in mind for upside potential.
Look for NNVC to make higher lows and higher highs. That is often the first sign of a more sustainable uptrend.
A strong close near the highs could help confirm a potential new leg higher.
A rally and close above the 20 day moving average of 1.56 could result in increased upside.
In addition, NNVC has a RSI of 44 – showing upside potential.
On Monday, the company announced:
“NanoViricides, Inc. Has Filed its Quarterly Report - Subsequent Raise Has Fortified Fiscal Position”
At present:
“There is no approved drug for Influenza that can be reliably predicted to be not escaped by the next potential epidemic or pandemic Influenza virus, including H5N1. All approved influenza drugs are known to be readily escaped by Influenza variants.”
“Additionally, in the current season, the mutated clade K of the A/H3N2 subtype is dominant in the Northern hemisphere, and the seasonal Influenza vaccine is "mismatched" (i.e. it contains the older variant, clade J, of A/H3N2). When the vaccine is mismatched, the overall vaccine efficacy as determined post-season has been as low as 11-17% [1].”
“There is no approved drug for RSV, although three different antibodies have been approved for pre-exposure protection of infants from potential risk of RSV infection, and some vaccines have been approved for use in geriatric patients and adults at risk, as well as for pregnant women. While the market size is projected to be exceeding $8 billion or so, the regulatory development timelines are long for RSV pediatric drug development.”
“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.”
“The approved drugs for Influenza are unlikely to meet the challenge of an H5N1 or highly pathogenic influenza virus epidemic.”
Importantly:
“NV-387, based on relevant animal model studies, and based on safety and tolerability observed in a Phase I human clinical trial, can fulfill these glaring gaps in pandemic preparedness for current and emerging threats, as well as for potential bioterrorism threats.”
“Thus, NV-387, as a single drug, is responding to several unmet medical needs in viral infectious diseases at once.”
Current Quarter Developments:
“During the current quarter, we have diligently continued our progress towards initiating a Phase II human safety and effectiveness clinical trial for the evaluation of NV-387 as a treatment of Monkeypox in the Democratic Republic of Congo.”
“The local regulatory agency, ACOREP, has already approved this Phase II clinical trial, subject to completion of certain requirements.”
“Africa continues to suffer from the Monkeypox epidemic, which has resulted in the Africa CDC declaring in August 2024 a "Public Health Emergency of Continental Security" (PHECS), a status that continues because this epidemic has continued to expand across national boundaries. This Mpox epidemic is driven by the more morbid and more virulent versions, Clade 1a and 1b, as compared to the 2022 outbreak that was driven by the less virulent Clade 2. The latter has become endemic in the USA and the Western World, but remains limited to sexual transmission primarily in the men-having-sex-with-men (MSM) population. The case fatality rate of Clade 1 has been between 9% to 1.5%, whereas that of Clade 2 is less than 0.3%.”
“Our objective is to bring the data from the clinical trials external to the USA and utilize it for further regulatory advancement of NV-387 against various indications under the US FDA. NV-387 has certain orphan disease as well as bioterrorism related indications.”
“Therefore, we first plan to file the appropriate Orphan Drug Designations (ODD) for NV-387 as a treatment for MPOx, Smallpox, and also for Measles. The ODD if approved provides several benefits that would accelerate the NV-387 program towards regulatory licensure. These include frequent FDA meetings and rapid decision-making. Additionally, the economic benefits include certain tax credits for R&D costs, waiver of certain PDUFA fees, and a seven year exclusivity for marketing the drug for the licensed indication.”
We are continuing to monitor NNVC for a sustainable breakout higher.
Sources: PR1, PR2, PR3, PR4, PR5, PR6, PR6, PR7, PR8, PR9, PR10, PR11, PR12, PR13, PR14, Website, Chart
Happy Trading!
SmallCapStocks Team
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