News: ACADIA Pharmaceuticals Inc (ACAD.O)
ACAD.O on Consolidated Issue listed on NASDAQ Global Market
14.25USD
20 May 2013
14.25USD
20 May 2013
Price Change (% chg)
$0.98 (+7.39%)
$0.98 (+7.39%)
Prev Close
$13.27
$13.27
Open
$13.46
$13.46
Day's High
$14.75
$14.75
Day's Low
$13.40
$13.40
Volume
5,516,317
5,516,317
Avg. Vol
3,734,067
3,734,067
52-wk High
$14.75
$14.75
52-wk Low
$1.29
$1.29
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Thu, Apr 11 2013
Acadia says data from Parkinson's trial enough to file for approval
- Acadia Pharmaceuticals Inc said data from an initial late-stage trial would be sufficient to file for approval for its experimental antipsychotic drug for Parkinson's disease patients, and that it would not need to conduct an additional trial as planned earlier.
BRIEF-ACADIA Pharma up in premarket after phase III pimavanserin study data
NEW YORK, March 21 - ACADIA Pharmaceuticals Inc : * Pharma up 6.5 percent to $7.08 in premarket after phase III pimavanserin study data
UPDATE 1-Acadia antipsychotic for Parkinson's succeeds in trial
* Achieves antipsychotic effect without loss of motor function
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Press Releases
- ACADIA Pharmaceuticals Added to NASDAQ Biotechnology Index
- ACADIA Pharmaceuticals Prices Public Offering of Common Stock
- ACADIA Pharmaceuticals Announces Proposed Public Offering of Common Stock
- Faruqi & Faruqi, LLP Launches An Investigation Against ACADIA Pharmaceuticals Inc. (ACAD) For Potential Breaches Of Fiduciary Duties By Its Board Of Directors
- ACADIA Pharmaceuticals Reports First Quarter 2013 Financial Results
- ACADIA Pharmaceuticals to Announce First Quarter 2013 Financial Results on May 7, 2013
- ACADIA Pharmaceuticals to Present at the 12th Annual Needham Healthcare Conference on April 30, 2013
- GOFF Corporation Shares Halt The Slide Looking For Follow Through- Top Five Small Cap Stocks Ahead Of The Bell: Lyon Williams, Acadia Pharmaceutical, Fannie Mae, AMR Corporation
- Retailers Push Stocks Higher and Pfizer Inc. hits a new 52-Week High
- ACADIA Pharmaceuticals Announces Expedited Path to NDA Filing for Pimavanserin Following Meeting with FDA

