Alterity Therapeutics Limited, (ASX: ATH, NASDAQ: ATHE)
(“Alterity” or “the Company”) will present clinical data from its
lead drug candidate PBT434 at the American Academy of Neurology
Annual Meeting in Philadelphia, USA, from 5-9th May 2019.
Alterity will feature prominently at the Annual Meeting with a
Platform Presentation on Sunday 5th May featuring data from the
company’s Phase 1 clinical trial and a Poster Presentation
featuring pre-clinical data on Thursday 9th May.
The American Academy of Neurology Annual Meeting is one of the
largest gatherings of clinicians and researchers focusing on
neurology in the world. It has been running for more than 70
years.
The Platform Presentation is titled: A First in Human Study of
PBT434, a Novel Small Molecule Inhibitor of α-Synuclein Aggregation
and will present first data from the current clinical study
program. Details of this presentation, which is to be delivered by
David Stamler, MD, Chief Medical Officer & Senior VP Clinical
Development, will be disclosed to investors concurrently with the
presentation.
The Phase 1 Clinical Trial for PBT434 commenced in 2018 in
Australia, recruiting healthy adult and older adult (≥ 65)
volunteers with the primary goals of assessing the safety and
tolerability of PBT434 after single and multiple oral dose
administration. Secondary goals include evaluating pharmacokinetic
measures that will allow Alterity understand how PBT434 is absorbed
and metabolised by the body.
The Poster Presentation appearing on Thursday 9th May is titled:
PBT434 Prevents α-Synuclein Aggregation, Neuron Loss, Motor
Dysfunction and Reduces Glial Cell Inclusions in a Transgenic Mouse
Model of Multiple System Atrophy1.
This study evaluated the efficacy of PBT434 in a mouse model of
multiple system atrophy (MSA), which is a rare and rapidly
progressive neurological disorder that affects adults. MSA is
characterized by motor symptoms similar to those found in
Parkinson’s disease, loss of ability to coordinate voluntary
movements, and impaired ability to regulate involuntary body
functions such as blood pressure, bowel and bladder control and
sexual function. Symptoms typically commence between the ages of 50
and 60 years of age and it has no known cause. The Poster will be
lodged to coincide with the session later in the week.
PBT434 is the first of a new generation of small molecules
designed to block the accumulation and aggregation of α-synuclein.
α-synuclein is of great interest because aggregated forms of the
protein are considered a pathological hallmark of Parkinsonian
conditions and are a recognised therapeutic target by
neuroscientists and clinicians.
Session details:
Oral Presentation Session:
- First in Human Study of PBT434, a Novel
Small Molecule Inhibitor of α-Synuclein Aggregation
- Session S4: Clinical Trials in Movement
Disorders, Sunday May 5, 1:00 pm US ET
- Presentation number 001
Poster Presentation Sessions:
- Abstract number 837; PBT434 Prevents
α-Synuclein Aggregation, Neuron Loss, Motor Dysfunction and Reduces
Glial Cell Inclusions in a Transgenic Mouse Model of Multiple
System Atrophy2
- Poster Session P5, Thursday May 9,
11:30am to 6:30pm US ET
- Poster presentation number 8-006
Geoffrey Kempler, CEO and Chairman said: “The AAN is the most
prestigious gathering of clinicians and researching working in
neurology and we are very pleased to have such strong participation
which speaks to the novelty and promise of our PBT434 drug
candidate for the treatment of neurological diseases.”
End Note
The Company changed its name on 8 April 2019 from Prana
Biotechnology Limited to Alterity Therapeutics Limited, (ASX: ATH,
NASDAQ:ATHE).
Investor enquiries IR@altertitytherapeutics.com
About Alterity Therapeutics Limited
Alterity’s lead candidate, PBT434, is the first of a new
generation of small molecules designed to inhibit the aggregation
of pathological proteins implicated in neurodegeneration. PBT434
has been shown to reduce abnormal accumulation of α-synuclein and
tau proteins in animal models of disease by restoring normal iron
balance in the brain. In this way, it has excellent potential to
treat various forms of atypical Parkinsonism such as Multiple
System Atrophy (MSA) and Progressive Supranuclear Palsy (PSP).
For further information please visit the Company’s web site at
www.alteritytherapeutics.com.
Forward Looking Statements
This press release contains "forward-looking statements" within
the meaning of section 27A of the Securities Act of 1933 and
section 21E of the Securities Exchange Act of 1934. The Company has
tried to identify such forward-looking statements by use of such
words as "expects," "intends," "hopes," "anticipates," "believes,"
"could," "may," "evidences" and "estimates," and other similar
expressions, but these words are not the exclusive means of
identifying such statements.
Important factors that could cause actual results to differ
materially from those indicated by such forward-looking statements
are described in the sections titled “Risk Factors” in the
Company’s filings with the SEC, including its most recent Annual
Report on Form 20-F as well as reports on Form 6-K, including, but
not limited to the following: statements relating to the Company's
drug development program, including, but not limited to the
initiation, progress and outcomes of clinical trials of the
Company's drug development program, including, but not limited to,
PBT434, and any other statements that are not historical facts.
Such statements involve risks and uncertainties, including, but not
limited to, those risks and uncertainties relating to the
difficulties or delays in financing, development, testing,
regulatory approval, production and marketing of the Company’s drug
components, including, but not limited to, PBT434, the ability of
the Company to procure additional future sources of financing,
unexpected adverse side effects or inadequate therapeutic efficacy
of the Company's drug compounds, including, but not limited to,
PBT434, that could slow or prevent products coming to market, the
uncertainty of patent protection for the Company's intellectual
property or trade secrets, including, but not limited to, the
intellectual property relating to PBT434.
Any forward-looking statement made by us in this press release
is based only on information currently available to us and speaks
only as of the date on which it is made. We undertake no obligation
to publicly updated any forward-looking statement, whether written
or oral, that may be made from time to time, whether as a result of
new information, future developments or otherwise.
1 PBT434 Prevents α-synuclein Aggregation, Neuron Loss, Motor
Dysfunction and Reduces Glial Cell Inclusions in a Transgenic Mouse
Model of Multiple System Atrophy [David Finkelstein1, Nadia
Stefanova2, Paul Adlard1, Margaret Bradbury3, David Stamler3
1Florey Institute of Neuroscience, 2Medical University of
Innsbruck, 3Prana Biotechnology]
2 PBT434 Prevents α-synuclein Aggregation, Neuron Loss, Motor
Dysfunction and Reduces Glial Cell Inclusions in a Transgenic Mouse
Model of Multiple System Atrophy [David Finkelstein1, Nadia
Stefanova2, Paul Adlard1, Margaret Bradbury3, David Stamler3
1Florey Institute of Neuroscience, 2Medical University of
Innsbruck, 3Prana Biotechnology]
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Investor RelationsRebecca WilsonE:
rwilson@buchanwe.com.auTp: +61 3 9866 4722
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