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| Alias Born | 10/19/2008 |
Thursday, June 06, 2019 4:35:28 PM
The FDA does some good things, but they also force a lot of bullshit and costs that get in the way of human trials. ISCO went to Australia to avoid all that and get their therapeutic into 12 humans as soon as practical. All 12 had well tolerated procedures which is great. The FDA also considers safety and efficacy data from credible institutions around the world, such as the Florey Institute of Neuroscience in Australia, when evaluating further studies along the same or related lines.
Recent ISCO News
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 05/14/2026 08:00:37 PM
- Form ARS - Annual Report to Security Holders • Edgar (US Regulatory) • 04/29/2026 08:35:02 PM
- Form 10-K - Annual report [Section 13 and 15(d), not S-K Item 405] • Edgar (US Regulatory) • 03/30/2026 09:29:18 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 11/18/2025 10:18:02 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 11/13/2025 09:00:53 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 09/16/2025 01:57:40 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 06/20/2025 12:21:17 PM
