'You're spot on malmanu. BSI will await results of FDA initial 20 patient safety assessment before even reconsidering CE approval'
You may be right, or not.
If so then it will be a long wait.
As OSL are so keen to try and draw a comparison with SRX, lets look at the current phase 1 for kidney treatment from SRX. With a product that had a PMA in 2002, and with many thousands of treatments, a new indication for Kidney has taken over 2 years to recruit 24 pts. Maybe SRX are just incompetent.
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- Ann: FDA IDE Approval-OSL.AX
OSL
oncosil medical ltd
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Ann: FDA IDE Approval-OSL.AX, page-49
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Last
$1.16 |
Change
-0.075(6.10%) |
Mkt cap ! $16.35M |
Open | High | Low | Value | Volume |
$1.25 | $1.25 | $1.11 | $45.63K | 37.86K |
Buyers (Bids)
No. | Vol. | Price($) |
---|---|---|
2 | 16333 | $1.15 |
Sellers (Offers)
Price($) | Vol. | No. |
---|---|---|
$1.18 | 576 | 1 |
View Market Depth
No. | Vol. | Price($) |
---|---|---|
2 | 16333 | 1.150 |
1 | 15000 | 1.105 |
1 | 7500 | 1.080 |
2 | 19761 | 1.050 |
1 | 2500 | 1.030 |
Price($) | Vol. | No. |
---|---|---|
1.180 | 576 | 1 |
1.195 | 6673 | 1 |
1.200 | 10635 | 2 |
1.245 | 2418 | 1 |
1.250 | 46027 | 1 |
Last trade - 14.28pm 27/06/2025 (20 minute delay) ? |
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PAR
PARADIGM BIOPHARMACEUTICALS LIMITED..
Paul Rennie, MD & Founder
Paul Rennie
MD & Founder
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