SI
SI
discoversearch

We've detected that you're using an ad content blocking browser plug-in or feature. Ads provide a critical source of revenue to the continued operation of Silicon Investor.  We ask that you disable ad blocking while on Silicon Investor in the best interests of our community.  If you are not using an ad blocker but are still receiving this message, make sure your browser's tracking protection is set to the 'standard' level.
Biotech / Medical : ARIAD Pharmaceuticals -- Ignore unavailable to you. Want to Upgrade?


To: jaybe who wrote (3250)2/25/2014 9:43:38 PM
From: HerefordRibSteak  Read Replies (1) | Respond to of 4474
 
jaybe,
What would be the estimated market size(s) of your predicted MET/RON or Her2/Her3?

TIA

HRS



To: jaybe who wrote (3250)2/26/2014 12:15:35 AM
From: tejek  Read Replies (1) | Respond to of 4474
 
. My problem with KIT, PDGFR, VEGFR, FGFR, FLT3 or RET is why advance a candidate in late 2014 that diminishes Pona's potential. In a supposed shareholder value creating year this wouldn't make sense. I think the new candidate was expedited due to its marketable expansion of pipeline, lab expertise, and revenue potential.

Footnote: Interesting that HB stated [Nature Biotech Podcast in [Sept 2013] his personal goal of seeing next two candidates into clinical trials. To me this means the second candidate (3rd gen EGFRm) will not be far behind, likely by mid-2015. Since both candidates were described in late 2012 as progressing well both could be IND ready this year.

He's been talking about a new candidate for some time now. Why does it take so long to get into clinical trials?



To: jaybe who wrote (3250)2/26/2014 2:03:36 PM
From: Biomaven  Read Replies (1) | Respond to of 4474
 
>>I think HB's pan-inhibitor means targeting the kinase and known mutations as well as potentially alternate activated pathways such as PI3K

Unclear to me because they used the term "pan-inhibitor" for pona to mean it inhibits all (single) mutations of the target. Nothing about alternate pathways there.

I wouldn't call RON clinically validated at this point at all, and MET inhibitors still have considerable doubt associated with them.

Something like a pan-KIT inhibitor would fit their descriptions better. There are a class of mutations that none of the existing drugs (including pona) can handle well. Not sure how excited the market would be, but it is a significant opportunity with GIST prevalence increasing considerably.

EGFRm is really competitive these days.

Peter