No but he should get the blame if there are serious adverse events from drugs released to the general population with shortened trials. Or if drugs that are not efficacious are released. It’s quite possible US FDA approval may not be considered valid internationally if the trial process Is shortened significantly.
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pyc therapeutics limited
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Ann: First Subject Dosed in PKD Clinical Trial, page-27
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$1.30 |
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Open | High | Low | Value | Volume |
$1.27 | $1.31 | $1.27 | $258.9K | 200.2K |
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No. | Vol. | Price($) |
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Price($) | Vol. | No. |
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No. | Vol. | Price($) |
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2 | 3158 | 1.270 |
2 | 15305 | 1.265 |
2 | 16318 | 1.260 |
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Price($) | Vol. | No. |
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1.295 | 27132 | 2 |
1.300 | 67329 | 2 |
1.305 | 1318 | 1 |
1.310 | 1318 | 1 |
1.315 | 1318 | 1 |
Last trade - 16.10pm 30/06/2025 (20 minute delay) ? |
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