Sunday, April 02, 2017 9:08:44 PM
There are process chemists with decades of experience in the pharma industry in scaling up difficult schemes.
How many of those know how to scale up amphiphilic self-assembling polymeric nanomicelles of uniform 20 nm diameter, with attachment points for ligands?
The cost in hiring such experts as full time employees
The PhD experts working on the problem are not NNVC employees. They work for Theracour. It's just like NNVC hired Theracour to do the work you are saying that NNVC should hire someone to do.
spending the millions to install the infrastructure to support that capability in-house doesn't make sense for any startup pharma.
That's why NNVC didn't hire them. They are paying Theracour to complete the project.
Characterizing metabolites is done as part of the ADME work done by the same GLP certified labs doing the IND enabling studies.
Once again, how many have experience in characterizing metabolites of a never before created nanomedicine? I'm guessing almost none.
it makes no sense for a startup to spend the millions for setting up that capability in house.
Glad that you agree with NNVC's strategy of not having these people in house. The work is contracted out to Theracour.
If NNVC has a single lead candidate as Seymour claims, there is no conceivable in-house work that could be done to further its development
That is nonsense. NNVC hired a virologist to screen all the drug candidates in vitro, and possibly in vivo. It's important work that saves on drug development time by not contracting that work out and waiting for results. It can be run on NNVC's schedule.
Can't have it both ways - criticizing the outside lab testing then saying that "there is no conceivable in-house work that could be done." It is better to have an in-house virologist do the majority of the screening, then have outside experts validate and further the findings in different models. Similarly, it is better that NNVC hire out the scale-up and metabolite characterization work to Theracour. NNVC has a decent strategy to conserve funds. Hopefully, Theracour and the outside labs will come through, and NNVC will be in clinical testing before too long.
Recent NNVC News
- 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
- Form 8-K - Current report • Edgar (US Regulatory) • 10/01/2025 09:07:54 PM
