MSB themselves are guiding analysts and shareholders to expect a future adult GvHD trial as a backup to Ruxolitinib:
So they are aiming to be a third-line treatment. I’m not sure how much clearer the point can be made: Adult HR-aGvHD is still a wide open market for Cynata to target. As for off-label use, I think Pfeifer summed it up pretty clearly. If you think that clinicians are going to prioritise a therapy approved for a tiny portion of a subset of a disease, where the company who make said therapy are openly telling you it should be used as a last resort, then I have some magic beans I would like to sell you.
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cynata therapeutics limited
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CYP Price Target post MSB FDA approval., page-125
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Last
16.5¢ |
Change
0.000(0.00%) |
Mkt cap ! $37.28M |
Open | High | Low | Value | Volume |
0.0¢ | 0.0¢ | 0.0¢ | $0 | 0 |
Buyers (Bids)
No. | Vol. | Price($) |
---|---|---|
5 | 277439 | 16.5¢ |
Sellers (Offers)
Price($) | Vol. | No. |
---|---|---|
17.0¢ | 44900 | 4 |
View Market Depth
No. | Vol. | Price($) |
---|---|---|
5 | 277439 | 0.165 |
9 | 1313831 | 0.160 |
3 | 26451 | 0.155 |
3 | 115000 | 0.150 |
3 | 48937 | 0.140 |
Price($) | Vol. | No. |
---|---|---|
0.170 | 44900 | 4 |
0.175 | 26397 | 3 |
0.180 | 113494 | 5 |
0.185 | 116765 | 4 |
0.190 | 143868 | 3 |
Last trade - 13.31pm 17/06/2025 (20 minute delay) ? |
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