Investigative studies are underway testing
Ketamir-2 as the potential first at home ketamine analog treatment
for PTSD, depression, and neuropathic pain, including cancer
pain
MIAMI, May 20, 2024
/PRNewswire/ -- MIRA Pharmaceuticals, Inc. (NASDAQ:
MIRA) ("MIRA" or the "Company"), a pre-clinical-stage
pharmaceutical company focused on the treatment of neurologic and
neuropsychiatric disorders, announced that it has advanced new
preclinical studies using Ketamir-2, its differentiated oral
ketamine analog, towards clinical development for the treatment of
severe post-traumatic stress disorder (PTSD) and other leading
mental health disorders and neuropathic pain indications.
Mira Pharmaceuticals Advances Preclinical
Trials Towards an IND Submission This Year for Ketamir-2
MIRA continues to advance studies of Ketamir-2 in animal
studies while improving manufacturing optimization as the company
prepares for human testing in 2025.
MIRA anticipates that positive results from these preclinical
studies will enable the submission of an Investigational New Drug
Application (IND) to the U.S. Food and Drug Administration (FDA) by
the end of this year, which if cleared by FDA would allow for human
clinical testing of Ketamir-2.
Development Update:
Initiation of Preclinical Trials with Pharmaseed for
PTSD
MIRA has initiated a preclinical trial in collaboration with
Pharmaseed Ltd ("Pharmaseed") to evaluate the efficacy of
Ketamir-2 as compared with Ketamine in a rat model of severe PTSD.
This study, designed to assess the alleviation of symptoms of
chronic stress and behavioral consequences of dysfunctional
processing of fear and fear memory, leverages established models
demonstrating the effectiveness of ketamine in treating PTSD
symptoms. While ketamine has demonstrated rapid and sustained
reduction in PTSD symptoms in several clinical studies, it has to
be given through intravenous, intramuscular or intranasal
administration. The current study is designed to provide
robust data on the potential for the orally administered Ketamir-2
through behavioral tests, biomarker analysis, and
immunohistochemistry to support future clinical applications.
Ongoing studies at Pharmaseed are already exploring the potential
of Ketamir-2 in treating depression and several forms of pain,
including neuropathic pain.
Head-to-Head Preclinical Study to be Conducted by Biotrial,
Inc. for Locomotor Activity Evaluation of Ketamir-2 Compared to
Ketamine
In parallel, MIRA has initiated a study with Biotrial,
Inc. (Biotrial) to evaluate the acute effects of Ketamir-2 on
spontaneous locomotor activity in mice. This study will assess
Ketamir-2's impact compared to ketamine and a control vehicle,
providing crucial data on the pharmacodynamics of Ketamir-2.
Ketamine is known to produce a biphasic effect on locomotion
(meaning high and low doses of ketamine have very different
effects). The initial hypolocomotion (reduced movement) phase
observed in rodents after ketamine administration is consistent
with the sedative and dissociative effects reported with ketamine
in humans, which can lead to impaired coordination and motor
function. The subsequent hyperlocomotion (increased movement) phase
in rodents mirrors the agitation, confusion and psychotic effects
seen in humans, particularly at higher doses of ketamine.
Since Ketamir-2 has a different chemical profile that
ketamine, MIRA anticipates that these head-to-head studies can be
predictive of Ketamir-2's side-effect profile in humans.
Initiation of 7-Day Animal Studies with
Frontage
MIRA is also advancing towards regulatory IND-enabling study and
has also initiated 7-day rat and dog toxicology studies with
Frontage Laboratories. These studies are critical steps towards
ensuring the safety and efficacy of Ketamir-2 in preparation for
human clinical trials.
Advancements in Ketamir-2 Manufacturing
In recent weeks, MIRA has also made significant advancements in
the manufacturing process of Ketamir-2, markedly simplifying and
optimizing the synthetic process while reducing production costs
and overall cost of goods. These improvements are critical as
MIRA scales up production under Good Manufacturing Practices (GMP)
to enable the required regulatory toxicology studies and to prepare
for an IND for Ketamir-2 submission later this year.
Potential of Ketamir for PTSD Treatment
According to the National Institutes of Health, PTSD affects
approximately 8 million adults annually in the United States, with current treatments
often providing limited relief and significant side effects.
Ketamir-2, as an oral ketamine analog, offers a promising
alternative due to its potential for ultra-rapid antidepressant
effects and improved safety profile. Unlike traditional SSRIs and
benzodiazepines, Ketamir-2 targets NMDA receptors in the brain,
which play a crucial role in synaptic plasticity and cognitive
function, potentially offering more effective and faster relief
from PTSD symptoms.
Exploring Collaborations for Cancer Pain Studies
In addition to its current initiatives, MIRA is also in
discussions with several research centers to potentially
collaborate on studying Ketamir-2's efficacy in treating cancer
pain. These collaborations could expedite the IND submission for
Ketamir-2 and the commencement of human clinical trials, while
increasing the potential therapeutic applications of Ketamir-2.
Management Comments
Erez Aminov, Chairman and CEO of
Mira Pharmaceuticals, commented, "The initiation of these
preclinical trials represents a significant milestone in our
mission to develop next-generation treatments for severe mental
health disorders as well as neuropathic pain. Our
collaboration with Pharmaseed and Biotrial underscores our
commitment to advancing Ketamir-2 towards clinical development in
humans and addressing the urgent needs of those suffering from PTSD
and other debilitating conditions. The financial impact of
medication-treated major depressive disorder in the U.S. stands at
an overwhelming $92.7 billion
annually, with $43.8 billion (47.2%)
of this amount due to treatment-resistant depression1.
Additionally, the U.S. market for post-traumatic stress
disorder treatments is on a significant rise, projected to reach
$26 billion by
20312. We are hopeful that Ketamir-2 can help
address these critical public health issues."
Dr. Itzchak Angel, Chief
Scientific Advisor of Mira Pharmaceuticals, added, "The data
generated from these studies will be invaluable in demonstrating
Ketamir-2's potential benefits. What sets Ketamir-2 apart from
ketamine is its high oral bioavailability and lack of mu opioid
interaction. As a result, Ketamir-2 potentially offers a safer and
more effective option for oral administration, providing rapid
relief for depression in a home setting. We are excited about
the progress we have made in simplifying the drug's manufacturing
process and are hopeful that Ketamir-2 can offer new hope for
patients with PTSD and other mental health and pain
conditions."
About MIRA Pharmaceuticals, Inc.
MIRA Pharmaceuticals, Inc. (Nasdaq: MIRA) is a
pre-clinical-stage pharmaceutical development company with two
neuroscience programs targeting a broad range of neurologic and
neuropsychiatric disorders. MIRA holds the exclusive U.S.,
Canadian and Mexican rights for Ketamir-2, a novel, patent
pending oral ketamine analog under investigation to potentially
deliver ultra-rapid antidepressant effects, providing hope for
individuals battling treatment-resistant depression, major
depressive disorder with suicidal ideation and post-traumatic
stress disorder. The U.S. Drug Enforcement Administration's
scientific review of Ketamir-2 concluded that it would not be
considered a controlled substance or listed chemical under the
Controlled Substances Act and its governing regulations.
In addition, MIRA's novel oral pharmaceutical
marijuana, MIRA-55, is currently under investigation for
treating adult patients suffering from anxiety and cognitive
decline, often associated with early-stage dementia. MIRA-55,
if approved by the FDA, could mark a significant advancement in
addressing various neuropsychiatric, inflammatory, and neurologic
diseases and disorders.
Additional information about the Company is available
at: www.mirapharmaceuticals.com.
Ketamir-2 and MIRA-55 are in early stage
pre-clinical development. There is no assurance that the products
will proceed through development or will receive FDA approval for
marketing.
___________________________
|
1 The
Journal of Clinical Psychiatry, PMID: 33989464
|
2 Allied
Market Research: Post-Traumatic Stress Disorder Treatment Market
Research, 2031
|
Cautionary Note Regarding Forward-Looking Statements
This press release and the statements of the Company's
management related thereto contains "forward-looking statements,"
which are statements other than historical facts made pursuant to
the safe harbor provisions of Section 27A of the Securities Act of
1933, as amended, and Section 21E of the Securities Exchange Act of
1934, as amended. These statements may be identified by words such
as "Aims," "anticipates," "believes," "could," "estimates,"
"expects," "forecasts," "goal," "intends," "may," "plans,"
"possible," "potential," "seeks," "will," and variations of these
words or similar expressions that are intended to identify
forward-looking statements. Any statements in this press
release that are not historical facts may be deemed
forward-looking. These forward-looking statements include, without
limitation, statements regarding Ketamir-2's potential in treating
certain mental health conditions or neuropathic pain and statements
regarding the timing for the Company's preclinical studies and the
filing of an IND for Ketamir-2. Any forward-looking
statements in this press release are based on the Company's current
expectations, estimates and projections only as of the date of this
release and are subject to a number of risks and uncertainties
(many of which are beyond the Company's control) that could cause
actual results (including the anticipated benefits of the Company's
pre-clinical testing and pre-clinical data discussed herein) to
differ materially and adversely from those set forth in or implied
by such forward-looking statements. These and other risks
concerning the Company's programs and operations are described in
additional detail in Annual Report on Form 10-K for the year ended
December 31, 2023 and other SEC
filings, which are on file with the SEC
at www.sec.gov and the Company's website
at https://www.mirapharmaceuticals.com/investors/sec-filings.
The Company explicitly disclaims any obligation to update any
forward-looking statements except to the extent required by
law.
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SOURCE MIRA Pharmaceuticals, Inc.