Silo Pharma Announces Positive Results for Intranasal PTSD Treatment
23 Aprile 2024 - 2:15PM
Silo Pharma, Inc. (Nasdaq: SILO) (“Silo” or the “Company”), a
developmental stage biopharmaceutical company focused on developing
novel formulations and drug delivery systems for traditional
therapeutics and psychedelic treatments, today announced positive
data in the final validation report from the recent pharmacokinetic
(PK) study
of SPC-15, an intranasal prophylactic treatment for anxiety
and post-traumatic stress disorder (PTSD). The PK study was
conducted as part of non-GLP small animal dose-ranging study of
SPC-15 completed in February 2024.
The activity of SPC-15 in the subjects or the PK study was
evaluated over a 7-day repeat intranasal dose, including the
processes of absorption, distribution, and excretion. Time to peak
drug concentration (Tmax) occurred between 0.5 and 2 hours
following intranasal administration compared to 2 hours following
oral gavage administration. In previous findings from the non-GLP
study, SPC-15 demonstrated rapid absorption with good exposure over
a full 24-hour period, and based on these studies we determined an
optimal once-per-day human intranasal dosing.
Silo CEO Eric Weisblum commented, “Our evaluation of the PK
profile for SPC-15 indicates effective and consistent exposure from
intranasal administration of the drug. We believe these study
results will be substantially replicated in humans.”
Now completed, the non-GLP study will be followed by a
progressive intellectual and neurological deterioration (PIND)
study and then a GLP study, both slated to commence in 2024, and
both of which are additional required steps before submission of an
Investigational New Drug (IND) application for SPC-15 to the
FDA.
About SPC-15
SPC-15 is a novel serotonin 4 (5-HT4) receptor agonist that
utilizes biomarkers for the treatment of PTSD, anxiety, and other
stress-induced affective disorders. SPC-15 is being developed
as an intranasal medication. If clinically successful, SPC-15 could
qualify for the FDA’s streamlined 505(b)(2) regulatory pathway for
drug approval. Silo Pharma is conducting preclinical studies of
SPC-15 in collaboration with Columbia University under a sponsored
research agreement and option.
About Silo Pharma
Silo Pharma Inc. (Nasdaq: SILO) is a developmental stage
biopharmaceutical company developing novel therapeutics that
address underserved conditions including stress-induced psychiatric
disorders, chronic pain conditions, and central nervous system
(CNS) diseases. Silo focuses on developing traditional therapies
and psychedelic treatments in novel formulations and drug delivery
systems. The Company’s lead program, SPC-15, is an intranasal
treatment targeting PTSD and stress-induced anxiety disorders.
SP-26 is a time-release ketamine-loaded implant for fibromyalgia
and chronic pain relief. Silo’s two preclinical programs are
SPC-14, an intranasal compound for the treatment of Alzheimer’s
disease, and SPU-16, a CNS-homing peptide targeting multiple
sclerosis (MS). Silo’s research and development programs are
conducted through collaborations with Columbia University and the
University of Maryland, Baltimore. For more information, visit
www.silopharma.com and connect on social media at LinkedIn, X, and
Facebook.
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the actual results of Silo Pharma, Inc. (“Silo” or “the Company”)
to differ materially from the results expressed or implied by such
statements, including changes to anticipated sources of revenues,
future economic and competitive conditions, difficulties in
developing the Company’s technology platforms, retaining and
expanding the Company’s customer base, fluctuations in consumer
spending on the Company’s products and other factors. Accordingly,
although the Company believes that the expectations reflected in
such forward-looking statements are reasonable, there can be no
assurance that such expectations will prove to be correct. The
Company disclaims any obligations to publicly update or release any
revisions to the forward-looking information contained in this
presentation, whether as a result of new information, future
events, or otherwise, after the date of this presentation or to
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