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Biotech / Medical
ARIAD Pharmaceuticals
An SI Board Since September 1996
Posts SubjectMarks Bans Symbol
4474 134 0 ARIA
Emcee:  jaybe Type:  Moderated
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4024Perfect example: siliconinvestor.com (ARIA)—FDA approves Roche’s Alecensa (aletktom-12/11/2015
4023Sorry my bad. I don't know what I was thinking.testad-12/11/2015
4022wait a minute - you actually read and digest posts from tktom?tktomizwked-12/11/2015
4021testad, from you post, it looks like you don't realize that Ariad was createtktom-12/11/2015
4020Since 1991? You are saying that because you did not sell when the stock was up testad-12/11/2015
4019Looks like zero chance of a buy out now. This is a small company and the value ttktom-12/11/2015
4018Bullish cross in MACD and Stochastic oscillator. Technical 76% chance up at foxcsfnsie-12/9/2015
4017ASH posters available for download at Ariad Nordics... ariadnordics.eujaybe112/9/2015
4016It's academic since IMHO there will be a buyout within 60 days.Denner could civic08801-12/8/2015
4015In justification of the phase III and dose-range finding trials earlier in the ymulanoon2007-12/8/2015
4014Thanks again Jaybe for all that you contribute. If you were on the Scientific Adcivic08801-12/8/2015
4013For OPTIC 2L trial, if prior trial results hold... Nilotinib (400mg BID) shouldjaybe-12/8/2015
4012too short to show safety, and so will have little impact on actual sales even iftktom-12/7/2015
4011And, finally Biomaven final conclusion on the new Ariad trial, which is stunningtktom-12/7/2015
4010 DewDiligence[graphic] Monday, 12/07/15 03:14:26 PM Re: biomaven0 post# 198033 tktom-12/7/2015
4009I tend to agree with Biomaven, the new phase 3 trail is a complete waste of monetktom-12/7/2015
4008Dew with Pona approved as announced today to go into Phase III for Second line ycivic08801-12/7/2015
4007Here's the update on the pona label changes... Renal artery stenosis has bejaybe-12/6/2015
4006No, but likely changes consistent with 48-month data being presented Monday at Ajaybe-12/4/2015
4005Jaybe, do you by any chance know Ariad's modification requests for sectionjesspro-12/4/2015
4004Ariad recently submitted a request to modify sections 5.1 Vascular Occlusion andDonShimoda-12/4/2015
4003So you think NVS is sitting on their BUTT...? No—NVS is busy promoting Tasigna. DewDiligence_on_SI-12/4/2015
4002So you think NVS is sitting on their BUTT.. What do you think they will do? Tellcivic08801-12/4/2015
4001BTW In Europe Actavis' Gleevec is already approved. Roll-out starts after JuTwoPack-12/4/2015
4000The 2/1/16 launch date for generic Gleevec is not exactly news—it’s been known sDewDiligence_on_SI-12/4/2015
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