Friday, June 8, 2012

ASCO for RNAi Therapeutics in Line with Expectations, but Curious Nevertheless (Part II- Atu027)

With some delay, only mirroring the strange delay by the sponsor company, Silence Therapeutics, in disseminating the results, here are my thoughts on the Atu027 phase I results presented at this year's ASCO and some speculations on the potential corporate fate of Silence Therapeutics.  

For part I (ALN-VSP02 ASCO discussion) here.


AtuPLEX Delivery Tech Tolerated Up to Twice Dose Required for Endothelial Knockdown

In retrospect, the phase I Atu027 surprised to the upside, especially in that the relatively ‘unsophisticated’ (some would say simple = elegant) AtuPLEX formulation used was apparently well tolerated in humans at doses well above where we would expect target gene knockdown in endothelial cells, the target cell population of this RNAi delivery technology: the 0.18mg/kg in this study yielded plasma siRNA concentrations where noticeable knockdown was seen in preclinical monkey studies in endothelial cells, and 0.336mg/kg is the recommended dose for further studies.   

I should caution, however, that the PK data are strictly inferring endothelial cell knockdown in the lung (of monkeys) to knockdown in tumor endothelia.  Although the data indicate that AtuPLEX (unlike e.g. DACC for lung endothelia) has a fairly broad target spectrum of endothelia in various tissues, there are some slight differences.  

On the downside, this study in patients with advanced solid tumors failed to provide striking evidence that Atu027 has indeed anti-tumor efficacy.  Although not a primary goal of this dose-finding dose escalation study, with only a paucity of efficacy-related data collected in this trial (in stark contrast to Alnylam’s heroic efforts with ALN-VSP02), it would have been comforting to see more evidence of efficacy besides the two reported regressions of a lung and a liver met plus the ‘stable disease responses’ -which really mean little in the absence of a control group.  The biomarker data were certainly curious, but without disclosing the full dataset could have been as well a cherry-picking exercise.  On this note, I also would have liked for Silence Therapeutics to disclose the full PK dataset.  

Besides for the small patient numbers (33), an explanation for a possible failure to see anti-tumor efficacy could be the choice of target gene, PKN3 (downstream of PI3K), which is a new clinical molecular target in the oncology arena.  On the other hand, I am pleased to see others in the blogosphere point out that the choice of a higher-risk target may be more than compensated for by the differentiation value it brings.  So in this case, you not only have an RNAi mechanism of action, but also the drug target as two major value-adding differentiating factors (see the March of the Lemmings by Bruce Booth).  But if target choice eventually turned out to be a problem here, the Atu027 PK results represent an important de-risking for the AtuPLEX delivery platform.   


Financial worries to the fore 

I’m sure many will be happy that this trial has finally wrapped up (last patient dosing expected later this month).  However, this also means that the focus will now be on a much-feared financing; feared, because the last financings by Silence Therapeutics have been catastrophic to existing shareholders. It is a shame that Silence Therapeutics has failed to obtain any non-dilutive funding despite numerous opportunities.

Along with the disclosure of the ASCO presentation, the company thus announced in an quite unusual move that ‘advanced discussions’ were under way to raise 4-5M UK pounds.  Judging from the previous fund-raisings, this may well double the share count.  Despite such a dilutive capital raise, the terms for which would more likely than not be dictated by the new investors, it would still be preferable over a Marina Bio-style cash crunch.  Actually, from where I sit in my armchair, a combination between the two ‘second-tier’ players Silence Therapeutics and Marina Biotech does not look that illogical as long as can find ways to further cut down on cash burn.  Note that some of Marina Biotech’s important business relationships are with European companies: Debiopharm, Girindus, Novosom tech and IP, usiRNA IP from Denmark etc etc.  

I'll be watching intently as to what the next move will be...



7 comments:

Anonymous said...

A company formed by the merger of Marina Biotech and Silence Therapeutics would have by far the broadest RNAi and nucleic acid drug delivery portfolio in the industry.

Anonymous said...

One cash poor plus one cash poor equal two cash poor (larger cash poor), what they need is a better clinical program shows efficacy to make them (and RNAi in general) more attractive to investors.

Dirk Haussecker said...

I totally agree and would not exclude bankruptcies at this point either...

Anonymous said...

I don't see Marina Biotech or Silence Therapeutics declaring bankruptcy at this point. Marina has about $750K in debt and I believe Silence is debt free.

Tekmira and Alnylam have LNP tested and validated more than any other RNAi delivery technology at this point. But I have to believe that one delivery technology such as LNP will not be able to address all of the undruggable targets that RNAI brings into play. Having a broad portfolio of different delivery technologies should be an advantage in the future. It will just take longer to see a payoff. Marina and Silence seem to be pursuing this strategy.

Anonymous said...

looks like Silence's quandary is what to do next with this trial and how to formulate Phase II approach. Randomized safety has achieved beyond presumed necessay dose level. No obvious clue as which tumor to focus on for Phase II. As Dirk pointed out in this blog, the choice of target may not be as promising as the in vivo data suggested.

Anonymous said...

I think all these companies, Tekmira, Silence, Marina will be successful some day and find their niche.

Anonymous said...

Agree. They all need a good helmsman to help them sail through this difficult economy. Looking at Atu027 and ALNVSP02 results, delivery is not as difficult as advertised. With careful selection of disease and target, good result will emerge. Cancer is a very diverse and difficult disease target to tackle, PCSK9 project could be promising.

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