Monday, January 17, 2022 9:04:18 PM
To answer your question,
If the RDV concentration and dosages in the NV-CoV-2 injections was higher than RDV only injections, couldn't that be the determining factor in the survival? More RDV is the cause for the increased survival?
The NV-CoV-2 contains NO RDV, and it works better than RDV. Figure 4 from the rat lethal CoV infection model is what I showed, and here is the caption:
Figure 4:
Survival of NV-CoV-2 (Polymer) treated or untreated Rats infected with NL63 virus The untreated rats and the Vehicle-treated rats infected with the Cov-NL63 virus survived until Day 5. Rats treated daily with Remdesivir only, 10 mg/kg, survived 7.5 days. The rats treated with NV-CoV-2, 160 and 320 mg/kg, survived until Days 13.5 and 14, respectively (4A). Further the survival of the infected rats were dependent on the number of days and dosage of the drug, NV-CoV-2 polymer (4B).
So, it looks like the drug works, yes, to prolong survival in an animal model of acute CoV disease? or are these authors all making things up?
Some of the doses from the rat in vivo PK paper are for NV-CoV-2-R, not the amount of RDV encapsulated in NV-CoV-2-R. NV-CoV-2-R consists of NV-CoV-2 plus whatever amount of RDV is encapsulated inside.
The rat in vivo PK preprint figures all use plasma RDV divided by total RDV in the dose given in order to be able to compare the raw vs. NV-CoV-2-R encapsulated form.
RDV values in male rats plasma obtained (mg/mL) after 1st. and 5th injection of the drugs were normalized by dividing with the amount of RDV administered (mg/kg of rat body weight) and shown in Fig. 2 and Fig. 3.
So the plasma levels are for equivalent amount of RDV given as "raw" RDV (well combined with their SBECD) or RDV inside NV-CoV-2.
One potentially troubling note about the dosing ... I thought the doses given in general were pretty high. Medium dose is 160 mg/kg for rat /6.2 to convert to human equivalent = ~25 mg/kg, or for 60 kg patient that is 1.3 g. If it takes a while to make kg scale batches, that isn't very many doses, even if some of that 1.3 g is composed of remdesivir.
Recent NNVC News
- 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 • ACCESS Newswire • 05/26/2026 12:30:00 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 05/21/2026 10:01:46 AM
- Form 8-K - Current report • Edgar (US Regulatory) • 05/20/2026 08:30:33 PM
- NanoViricides Announces Closing of ~$2 Million Registered Direct Offering • ACCESS Newswire • 05/19/2026 03:55:00 AM
- Form 424B5 - Prospectus [Rule 424(b)(5)] • Edgar (US Regulatory) • 05/18/2026 12:45:22 PM
- Ebola Global Health Emergency Needs a Broad-Spectrum Drug - NV-387 is a Strong Potential Candidate, Says NanoViricides • ACCESS Newswire • 05/18/2026 12:30:00 PM
- NanoViricides Announces Pricing of ~$2 Million Registered Direct Offering • ACCESS Newswire • 05/15/2026 12:35:00 PM
- NanoViricides, Inc. Has Filed its Quarterly Report - NV-387 Advancing for Phase II • ACCESS Newswire • 05/15/2026 12:00:00 PM
- Recent Hantavirus On A Cruise Ship Highlights the Need for Broad-Spectrum Antiviral Drugs Such as NV-387, Says NanoViricides • ACCESS Newswire • 05/11/2026 12:30:00 PM
- NanoViricides, Inc. Announces Participation in the D. Boral Capital Global Conference • Newsfile • 05/06/2026 07:37:00 PM
- NV-387 for The Treatment of Measles is Granted Orphan Drug Designation by The US FDA • ACCESS Newswire • 05/04/2026 12:30:00 PM
- Deadly Measles Cases Accentuate the Need for a Treatment - NV-387 is Here to Help Patients and Control Spread, Says NanoViricides • ACCESS Newswire • 04/21/2026 12:30:00 PM
- Measles Rare Pediatric Disease Drug Designation Application Filed for NV-387, PRV Provides for Strong Business Case, Says NanoViricides • ACCESS Newswire • 04/07/2026 12:30:00 PM
- Phase II Clinical Trial of Monkeypox Treatment by NV-387 to Commence Soon, Announces NanoViricides • ACCESS Newswire • 04/01/2026 12:30:00 PM
- NanoViricides Presenting at NIBA's 152nd Investment Conference in Fort Lauderdale, FL March 12, 2026 - Announces Manufacture of Phase II Clinical Product NV-387 Oral Gummies is Complete • ACCESS Newswire • 03/11/2026 12:30:00 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 02/17/2026 09:30:47 PM
- MPox Orphan Drug Designation Application Filed for NV-387, Declares NanoViricides • ACCESS Newswire • 02/12/2026 01:30:00 PM
- Measles Orphan Drug Designation Application Filed for NV-387, Declares NanoViricides • ACCESS Newswire • 02/10/2026 01:30:00 PM
- Form 424B3 - Prospectus [Rule 424(b)(3)] • Edgar (US Regulatory) • 12/30/2025 09:30:18 PM
- Form DEL AM - Delaying amendment • Edgar (US Regulatory) • 12/16/2025 09:30:05 PM
- Form S-3 - Registration statement under Securities Act of 1933 • Edgar (US Regulatory) • 12/15/2025 09:26:07 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 11/26/2025 09:30:33 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 11/14/2025 09:32:10 PM
- Form 424B5 - Prospectus [Rule 424(b)(5)] • Edgar (US Regulatory) • 11/12/2025 07:54:28 PM
- Form 424B5 - Prospectus [Rule 424(b)(5)] • Edgar (US Regulatory) • 11/12/2025 04:29:54 PM
