They seem like fair questions to me(the eastern European bona fides)
At the end of the day they fall at the feet of the company implementing and supervising the trial, which wasn't ACL I believe...??
Again, I don't understand how x 40 to x 1000 delivery of the active ingredient to the site can possibly be a non event.
I know there are things in life where "more is not necessarily better" but if this is such a case,I suppose I won't be the only one wondering why.
Dr Reddy's and European and ROW approval of Fonda? The clock is ticking ..Anyone know when that might eventuate?
Add to My Watchlist
What is My Watchlist?
 (20min delay)
|
|||||
|
Last
1.0¢ |
Change
0.000(0.00%) |
Mkt cap ! $1.409M | |||
| Open | High | Low | Value | Volume |
| 0.0¢ | 0.0¢ | 0.0¢ | $0 | 0 |
| TSN (ASX) Chart |
Day chart unavailable