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Thursday, October 24, 2013 9:08:41 PM
Now, for all we know, NNVC is in the process of producing sufficient quantities of FluCide (reproducible)final candidate. However, this does not mean BASi is waiting with arms crossed for NanoViricides, Inc. to provide the first batch, meaning they are working on other projects. Maybe Tox and Safety studies have begun (to be announced Monday?). If not perhaps they could begin next week if BASi is open for the project to start. Possible?
BASi was with Nanoviricides, Inc. in the pre-IND meeting and the US FDA gave guidance beyond their documents. Is it possible that BASi's GLP Tox and Safety Studies were modified and shortened?
I know, we are not FAST TRACKed yet but thinking US FDA has gone way beyond their documents, even before fast-tracking further.
Recent NNVC News
- NanoViricides Reports that the Phase I NV-387 Clinical Trial is Completed Successfully and Data Lock is Expected Soon • InvestorsHub NewsWire • 05/02/2024 02:07:42 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 02/16/2024 09:53:32 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 02/14/2024 09:55:35 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 01/19/2024 09:44:48 PM
- Form DEF 14A - Other definitive proxy statements • Edgar (US Regulatory) • 12/04/2023 09:08:49 PM
- Form 10-K - Annual report [Section 13 and 15(d), not S-K Item 405] • Edgar (US Regulatory) • 10/13/2023 08:30:41 PM
- Form NT 10-K - Notification of inability to timely file Form 10-K 405, 10-K, 10-KSB 405, 10-KSB, 10-KT, or 10-KT405 • Edgar (US Regulatory) • 09/28/2023 08:44:54 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 09/01/2023 08:46:45 PM
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