News Focus
News Focus

12x

Followers 17
Posts 523
Boards Moderated 0
Alias Born 08/04/2022

12x

Re: Doc328 post# 498294

Monday, 08/18/2025 9:23:48 PM

Monday, August 18, 2025 9:23:48 PM

Post# of 517005

I don't think WS is attributing much of the market cap to Schizo.


Not much market cap for Schizo. Based on CGPT estimates on the scenarios you listed, the current attribution looks something like this:

-Excellent (>8-point PANSS, ~10% prob): ~$1B / +$10
-Good (6–8 pts, ~15% prob): ~$300M / +$3
-Anything else: $0

MAA approval (vs just next step in the process) would be huge but probably not in 2025 (imo unlikely at any time unless another P3).


Within MAA outcomes, what do you think of the likelihood of a conditional approval (CMA) as oppose to an outright rejection here? In CMA scenario, patients gain access to Blarcamesine, while EMA still get the large confirmatory trial (essentially a P3).

On timing: AVXL’s MAA review has been tracking Pridopidine’s path quite closely. For reference:

Pridopidine: 120d (8/15/24) ? LoQ (12/9/24) ? 121d (4/8/25) ? LoI (5/22/25) ? Oral Explanation (7/22/25) ? CHMP opion (7/25/25).

Blarcamesine: 120d (12/27/24) ? LoQ (4/22/25) ? 121d (7/21/25) ? LoI (Sep ’25) ? Oral Explanation (Nov ’25) ? CHMP opinion ([b]Nov ’25) ? possible EMA approval (Jan ’26) if positive.
Volume:
Day Range:
Bid:
Ask:
Last Trade Time:
Total Trades:
  • 1D
  • 1M
  • 3M
  • 6M
  • 1Y
  • 5Y
Recent AVXL News