OliX Announces Positive Preclinical Data in NASH Non-human Primate Models | |
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Date : 2022-11-10 View : 704 | |
OliX
Pharmaceuticals Announces Positive Preclinical Data in NASH Non-human Primate
Models SUWON, South Korea, Nov. 07, 2022 -- OliX Pharmaceuticals,
Inc. (KOSDAQ: 226950), a leading developer of
RNAi therapeutics, announced today that the Company
has secured positive effects of OLX702A, an investigational GalNAc-asiRNA
therapeutics for the treatment of nonalcoholic steatohepatitis (NASH), on liver
fat content in a non-human primate NASH model. According to the Company,
the administration of OLX702A resulted in a significant reduction in liver fat
content, measured by magnetic resonance imaging proton density fat fraction
(MRI-PDFF). Dose-dependent reductions in liver fat content up to 43% relative
to baseline were observed after administration of OLX702A, with liver fat contents
returning back to normal levels. No such effects were observed in the control
group supporting further evaluation of OLX702A for this indication which
presents as a major unmet medical need with no effective treatments available
to date. Aaron Hakim, M.D. affiliated
with Beth Israel Deaconess Medical Center and Harvard Medical School, and
member of the OliX Scientific Advisory Board said, "The OLX702A program is
based on compelling human genetic evidence which suggests that knockdown of
this target may reduce liver fat, inflammation, and fibrosis and protect
against liver-related mortality. These preclinical results in NASH non-human
primates validate our human genetics-based approach to target selection at OliX
Pharmaceuticals. Once these data are confirmed in human NASH patients, they
will represent among the best MRI-PDFF reductions in the field." Dong Ki Lee, Ph.D., Founder and Chief Executive
Officer of OliX said, "Considering that
OLX702A has shown excellent efficacy not only in small animal models such as rodents
but also in non-human primate models that best resemble humans, we think we are
one step closer to the achievement of successful development of new drugs in
the future for this significantly ill patient population."
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