BetterLife Obtains Excellent Animal Cardiopulmonary Safety Data for Oral BETR-001
May 14 2024 - 7:00AM
BetterLife Pharma Inc. (“BetterLife” or the “Company”) (CSE: BETR
/ OTCQB: BETRF / FRA: NPAU), an emerging biotech company
focused on the development of BETR-001, a non-hallucinogenic
derivative of lysergic acid diethylamide (“LSD”), announced it has
completed its animal GLP cardiopulmonary safety study of BETR-001.
The study demonstrated that oral BETR-001 at doses over 100-fold
the projected starting dose in upcoming human trials did not show
any significant cardiopulmonary pharmacological safety issues in
animals.
Cardiopulmonary safety (also known as telemetry)
studies investigate the effect of a drug in animals using
surgically implanted transmitters to assess blood pressure,
electrocardiography (ECG), lung respiration, body temperature, and
general activity level. The BETR-001 cardiopulmonary study found no
BETR-001 related effects on ECG intervals, respiratory parameters,
core body temperature, or activity levels.
Dr. Ahmad Doroudian, CEO of BetterLife,
commented, “We are very excited about these findings. BETR-001 is a
unique non-hallucinogenic derivative of LSD with robust activity in
animal depression and anxiety models without the burden of being
hallucinogenic. Our previous in vitro neuroreceptor pharmacology
studies (Cell Report 2023) had shown that BETR-001 is not an
agonist at the 5-HT2B receptor. This is in marked contrast to LSD,
psilocybin, and many other serotonergic psychedelics which are
known to be agonists at the 5-HT2B receptor. Agonism at the 5-HT2B
receptor is a known cause of cardiac toxicity (Pharmacol. Ther.
2011). The clean safety profile of BETR-001 in our completed
cardiopulmonary study in animals further supports the claim that
BETR-001 demonstrates much better cardiac safety profile compared
to LSD, psilocybin and other serotonergic psychedelics with 5-HT2B
activity.”
Dr. Doroudian added, “We are currently
completing the remaining BETR-001 IND-enabling studies and project
to file the BETR-001 IND by end of 2024.”
The Company also announces that it has issued
1,035,342 common shares and 1,035,342 share purchase warrants
pursuant to the conversion of principal and accrued interest on
convertible debentures totalling $103,534.20. Share purchase
warrants are exercisable into common shares, on a one-for-one
basis, at an exercise price of $0.10 per warrant and expires on
December 31, 2025.
About BetterLife Pharma
BetterLife Pharma Inc. is an emerging
biotechnology company primarily focused on developing and
commercializing two compounds, BETR-001 and BETR-002, to treat
neuro-psychiatric and neurological disorders.
BETR-001, which is in preclinical and
IND-enabling studies, is a non-hallucinogenic and non- controlled
LSD derivative in development and it is unique in that it is
unregulated and therefore can be self-administered. BetterLife’s
synthesis patent for BETR-001 eliminates regulatory hurdles and its
pending patent, for composition and method of use, covers treatment
of major depressive disorder, anxiety disorder and neuropathic pain
and other neuro-psychiatric and neurological disorders.
BETR-002, which is in preclinical and
IND-enabling studies, is based on honokiol, the active anxiolytic
ingredient of magnolia bark. BetterLife’s pending method of use and
formulations patent covers treatment of anxiety related disorders
including benzodiazepine dependency.
BetterLife also owns a drug candidate for the
treatment of viral infections and is in the process of seeking
strategic alternatives for further development.
For further information, please
visit BetterLife Pharma.
Contact
David Melles, Investor Relations Manager Email:
David.Melles@blifepharma.comPhone: 1-778-887-1928
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news release. This news release contains forward-looking statements
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historical facts. Forward-looking statements are often identified
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reader is cautioned that assumptions used in the preparation of any
forward-looking information may prove to be incorrect. Events or
circumstances may cause actual results to differ materially from
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reliance on any forward-looking information. Such information,
although considered reasonable by management at the time of
preparation, may prove to be incorrect and actual results may
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