The pre-clinical and clinical data derived to date is always of some value. Besides, continuing PTX-200 in the clinic for AML was seen as a less than prudent use of funds given the crowded AML space. Funds are best directed towards PTX-100, giving PTX a foot in the door towards commercialisation.
The other thing to remember is that CellPryme is being kept going. It is a reiteration of PTX-200 for the enhancement of cell therapies, such as CAR-T. The evidence for our patent application just seems to grow: https://patentscope.wipo.int/search/en/detail.jsf?docId=WO2022241515
When we hear anything about third-party evaluations (by way of a licensing deal) is anyone's guess. Last we heard, CellPryme-A was on its way into the clinic (or so I thought).
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4.5¢ |
Change
0.001(2.27%) |
Mkt cap ! $36.23M |
Open | High | Low | Value | Volume |
4.5¢ | 4.6¢ | 4.5¢ | $6.007K | 133.4K |
Buyers (Bids)
No. | Vol. | Price($) |
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3 | 480817 | 4.5¢ |
Sellers (Offers)
Price($) | Vol. | No. |
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4.6¢ | 48908 | 1 |
View Market Depth
No. | Vol. | Price($) |
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3 | 480817 | 0.045 |
8 | 709226 | 0.044 |
2 | 212500 | 0.043 |
3 | 509476 | 0.042 |
6 | 371317 | 0.041 |
Price($) | Vol. | No. |
---|---|---|
0.046 | 48908 | 1 |
0.047 | 722704 | 3 |
0.053 | 347000 | 2 |
0.055 | 104000 | 2 |
0.056 | 57000 | 2 |
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James McDonnell, CEO
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