Hopefully some of our excellent contributors can help with this.
Fast forward 3 years and NNZ 2591 gets FDA approval for 2-3 of the current conditions, with 1-2 trials in P3.
Are we obliged to run safety trials every time we trial in a new condition or is there a real possibility that safety has been established and we can go straight to a P3/Registration trial?
Does that happen?
Hopefully some of our excellent contributors can help with...
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Last
$19.70 |
Change
0.520(2.71%) |
Mkt cap ! $2.515B | |||
| Open | High | Low | Value | Volume |
| $19.39 | $19.84 | $19.28 | $5.675M | 288.6K |
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| No. | Vol. | Price($) |
|---|---|---|
| 3 | 1531 | $19.66 |
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| Price($) | Vol. | No. |
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| $19.81 | 557 | 1 |
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| Last trade - 16.10pm 03/05/2024 (20 minute delay) ? |
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Last
$19.70 |
Change
0.520 ( 2.59 %) |
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| Open | High | Low | Volume | ||
| $19.50 | $19.84 | $19.28 | 87628 | ||
| Last updated 15.59pm 03/05/2024 ? | |||||
| NEU (ASX) Chart |