Wait ...what ? Am I understanding this correctly ?
alterity now has to do a 1 year preclinical study prior to advancing discussions with FDA on endpoints for a p2 ?
has the MSA route ( chosen to speed things up ) now backfired as no way to measure efficacy of p2 trial due to lack of data available so alterity now has to first produce said data ?
please tell me I'm wrong
Ann: Meeting with US FDA provides development path for ATH434, page-7
-
- There are more pages in this discussion • 7 more messages in this thread...
You’re viewing a single post only. To view the entire thread just sign in or Join Now (FREE)
Add ATH (ASX) to my watchlist
 (20min delay)
|
|||||
|
Last
0.3¢ |
Change
0.000(0.00%) |
Mkt cap ! $15.96M | |||
| Open | High | Low | Value | Volume |
| 0.4¢ | 0.4¢ | 0.3¢ | $2.733K | 832.4K |
Buyers (Bids)
| No. | Vol. | Price($) |
|---|---|---|
| 32 | 45274833 | 0.3¢ |
Sellers (Offers)
| Price($) | Vol. | No. |
|---|---|---|
| 0.4¢ | 126718541 | 16 |
View Market Depth
| Last trade - 15.57pm 09/08/2024 (20 minute delay) ? |
| ATH (ASX) Chart |