Today,
Ionis issued a press release revelaing that their drug candidate for Huntington’s
Disease was able to knock down the huntingtin target gene in a dose-dependent
manner. This is the first clinical
demonstration that single-stranded phosphorothioate antisense technology cannot
only engage gene targets, as had been shown in the gain-of-function approach
for spinal muscular atrophy (SPINRAZA; slide 58), but that it could do so in a
sufficiently robust manner so that a knockdown could be measured.
This, of
course, has broad implications for the Ionis antisense platform which is
similarly being developed for other RNaseH-based knockdown applications ranging
from the rare and severe (e.g. ALS, spinal cerebellar ataxias) to the more
common neurodegenerative diseases such as Alzheimer’s and Parkinson’s.
The reason
why this feat is remarkable and a great de-risking event for the technology is that in some of the
indications, the target gene is expressed and needs to be suppressed more or
less throughout the brain. Assuming Ionis
didn’t take brain biopsies, but instead looked for protein expression by taking
CSF samples which would +/- give you an average of target gene expression in
the entire CNS (a safe assumption), the ability to assess a dose-dependent gene knockdown is a testament
to the robustness of the gene knockdown.
The actual numbers,
however, remain under wraps as Ionis and partner Roche (which has exercised
its option to IONS-HTTRx in the wake of the data) plan to present them more
formally through a publication and a conference presentation with key thought leaders in the
disease present. My guess is that peak knockdown
is in the 50%+ range which Frank Bennett from Ionis has recently
referred to be in the desired knockdown range.
Given that dosing
in the study only lasted 3 months in this slowly progressive disease, it is
unlikely that actual clinical benefits will be reported from this phase I/IIa
study. But given the so called 'huntingtin knockdown holiday phenomenon' and some remarkable comments from investigators in the study and KOLs, one cannot but hope that we’ll
be in for a positive surprise.
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