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Friday, February 02, 2024 11:50:07 AM
But if a toxicity study can be initiated by end of February, give or take 4 to 6 weeks for results on a study of 12 - 18 rats, will bring us mid April for full toxicology report.
Submission to FDA and back and forth for trial design will take another 45 - 60 days.
Phase 1 trial, blinded study with 20 - 45 MS patients 3 to 6 months to measure a safety profile in humans will bring us to the Oct - Dec timeline.
If Orphan drug status can be obtained, then we would only need to complete a phase 2 study and approval can be granted and drug combo can be sold while a on-going phase 3 is conducted.
I doubt many here are interested in staying well into 2025 for a phase 2, but a solid phase 1 with results could potentially bring us to 100 mil/150 mil market cap.
Let’s say we balloon to a 2 Billion O/S. Solid phase 1 get us to a median 125mil market cap and an approx .06/.065 share price.
Now the OTC isn’t a perfect market so we can either undershoot or overshoot that market cap. I’ve seen ghost shells trade 500 mil market cap with no real business.
No-one really knows what will happen here, but I like my chances with GSTC than I do with the mega millions.
Recent GSTC News
- Form NT 10-Q - Notification of inability to timely file Form 10-Q or 10-QSB • Edgar (US Regulatory) • 08/14/2024 07:23:46 PM
- Form NT 10-Q - Notification of inability to timely file Form 10-Q or 10-QSB • Edgar (US Regulatory) • 05/17/2024 08:05:07 PM
- Form NT 10-Q - Notification of inability to timely file Form 10-Q or 10-QSB • Edgar (US Regulatory) • 02/15/2024 04:33:13 PM
- Form 10-K - Annual report [Section 13 and 15(d), not S-K Item 405] • Edgar (US Regulatory) • 01/19/2024 10:13:47 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) • 01/02/2024 09:21:47 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 11/13/2023 05:32:02 PM
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