Alnylam program update
Based on a poster presentation at this year’s Amercian Society for Hematology meeting (ASH11), also the remaining target pick under Alnylam’s 5x15™ will be a SNALP-based program that targets a gene in the liver: Tmprss6 knockdown for the treatment of iron overload diseases. As such, all of Alnylam’s core clinical programs are SNALP-based. If you had looked at the pipeline 3 years ago, you would have thought that this was where Tekmira was heading. The challenge now will be to clinically mature the programs to a point (in 2015) where the package will be attractive enough for a company like Genzyme/Sanofi-Aventis to acquire the orphan drug company Alnylam for somewhere between $1.0-1.5B.
This development confirms signals that the company has recently started to send out (Rodman Renshaw investor note and comments in the Piper Jaffray presentation) namely that not only is Alnylam now advertising itself as a product, and not platform company, but that it is likely to be all about gene knockdown in the liver. Long gone seem the days when management predicted Alnylam to be the next Genentech. In light of the confrontation with Tekmira, this path opens up the possibility of a settlement whereby Alnylam is allowed continued access to SNALP for the 5 programs, with Tekmira getting full control over other SNALP applications in and especially outside the liver. As a product company that has committed on its programs, why bother with trying to control a platform which is giving Alnylam nothing but legal headaches.
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4 comments:
I suppose it's nit picking, but your link'd in reference says Chase was there for over 4 years:
General Counsel Alnylam Pharmaceuticals Public Company; 51-200 employees; ALNY; Biotechnology industry
May 2007 – November 2011 (4 years 7 months)
Is it becoming a little boring this witch hunt on Alnylam Dirk?You may be right but I doubt you have fully reviewed their position versus Tekmira's whose side you seem to take at the drop of a hat.How about a week or two talking about the core subject rather than your pet subject.As you can see from your loyal support there are people who believe in you and even trust your judgement.You risk marginalising followers and making them worry that you are an academic out of touch with the real world.
Steve- that's correct. I was falsely under the impression that he was the successor of Donna Ward (former for VP IP) who left a year ago.
Giles- it is my judgment that control of the industry's most advanced systemic delivery platform is critical to the future of RNAi Therapeutics. You may disagree, but the RNAi clinical pipeline development over the last 2 years where the majority of programs were based on SNALP, I believe shows that this is indeed the case. The strategies of major Big Pharma players such as Merck, Takeda and Novartis are also affected by this topic.
If you have topics you are interested to learn more about, but has not been covered on my blog, you can always commission one for your exclusive use.
Thanks for your blog, Dirk, please continue, there is none other that combines deep understanding of the science with a wide understanding of the RNAi investment world.
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