Tuesday, April 11, 2023 9:08:32 PM
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Send me $40K and I'll say ALMOST anything.
Diwan's name does not appear. Nor is their any mention of his relationship with the licensee.
And the Zach's Phd puts forth the same shaky proposition that NNVC's friend at Benzinga offered up:
"This is an important inflection point for NanoViricides as it is now transitioning to clinical-stage operations following a long development timeline as a pre-clinical company."
It is? NNVC is licensing 2 drugs to "someone else" to conduct the trials....the licensee will be conducting clinical-stage operations, not NNVC.
Some might say that that's just semantics. I prefer to call it misleading. And it's no small thing. Investors have been waiting for NNVC to run clinical trial for a long, long time....why aren't they actually doing it themselves, instead of just intimating that they are?
I didn't miss this.....
"Karveer has begun clinical development and evaluation of those two drugs and has obtained regulatory permissions to conduct clinical evaluation of them in India"
.....but it doesn't answer the question.
We've been we'll seeing for well over a decade.
Send me $40K and I'll say ALMOST anything.
Diwan's name does not appear. Nor is their any mention of his relationship with the licensee.
And the Zach's Phd puts forth the same shaky proposition that NNVC's friend at Benzinga offered up:
"This is an important inflection point for NanoViricides as it is now transitioning to clinical-stage operations following a long development timeline as a pre-clinical company."
It is? NNVC is licensing 2 drugs to "someone else" to conduct the trials....the licensee will be conducting clinical-stage operations, not NNVC.
Some might say that that's just semantics. I prefer to call it misleading. And it's no small thing. Investors have been waiting for NNVC to run clinical trial for a long, long time....why aren't they actually doing it themselves, instead of just intimating that they are?
I didn't miss this.....
"Karveer has begun clinical development and evaluation of those two drugs and has obtained regulatory permissions to conduct clinical evaluation of them in India"
.....but it doesn't answer the question.
We've been we'll seeing for well over a decade.
No matter what it is or who commenced it, I'm against it!
....Groucho
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
