Certain information contained within
this announcement is deemed by the Company to constitute inside
information. Upon the publication of this announcement via a
Regulatory Information Service, this inside information is now
considered to be in the public domain.
ANANDA DEVELOPMENTS
PLC
("Ananda"
or the "Company")
Phase 1 Pharmacokinetics
Study to be conducted on MRX1
Ananda Developments plc (AQSE: ANA),
a life sciences company focused on the research and clinical
development of therapies for a range of complex inflammatory pain
conditions, is pleased to announce that it has signed a contract
with Southern Star Research Pty
Ltd ('SSR'), a leading
Australian Contract Research Organisation, to carry out a Phase 1
clinical trial investigating the pharmacokinetic ("PK") profile,
tolerability and safety of the Company's lead investigative asset,
MRX1.
Highlights:
·
Contract signed for Phase 1 PK study
·
The clinical trial will investigate the PK
profile, tolerability and safety of MRX1 in healthy
volunteers
·
The data generated will inform future clinical
trials in patients and form an integral part of any future
regulatory applications, including with the MHRA in the United
Kingdom or FDA in the United States
·
Collected data will form part of Ananda's MRX1
patent estate and wider intellectual property portfolio
·
Significant financial advantages of running the
study in Australia, including an R&D Tax Incentive of up to
43.5% of eligible research and development costs
Ananda recently posted a blog about
the reasons for running a PK study which is available to
read here,
the slides from a recent event regarding the reasons behind running
a Phase 1 study in Australia are available
here and a summary video of this
announcement is also available on the Hub alongside the
RNS.
Ananda has elected to conduct this
Phase 1 study to provide in-human data on its MRX1 drug candidate,
specifically related to PK, tolerability,
and safety. This data will provide useful background information
when discussing MRX1 and the wider Ananda drug development pipeline
with potential investors, in partnering discussions with
pharmaceutical companies, and with clinician investigators for
clinical trials in other indications. Crucially, the study will
form a foundational piece of the data package for regulatory
filings.
Further to this, the findings from
the PK study can be used as a key data source for submission of an
Investigational New Drug ('IND') application to the Federal Drug
Administration ('FDA') in the United States - a key first step to
having a drug approved for use in the USA.
The next steps for the study are to
complete the trial protocol and finalise agreements with a
Phase 1 unit that will run the trial site, before progressing
to Human Research Ethics Committee ("HREC"), and a Clinical Trial
Notification will be filed with the Therapeutic Goods
Administration (Australian regulatory body) as well as securing a
Good Manufacturing Practice certification of the MRX1 drug
batch.
About the MRX1 Phase 1 PK study
The study will dose 20 healthy
volunteers with MRX1. It will measure PK levels following an acute
(single) dose, as well as chronic dosing (where the PK levels will
be measured over a period of six days) to investigate the
accumulation of MRX1 in the body over the course of the study. The
volunteers will be hospitalised for the duration of the study and
include equal numbers of males and females.
Conducting the study in Australia
The study will be conducted in
Australia because it has a vibrant Phase 1 offering and financial
advantages. The Australia Tax Office offers a 43.5% cash rebate on
all Research & Development work undertaken in
Australia. The study will be conducted via Ananda's
wholly owned Australian subsidiary, Tiamat Australia Pty
Ltd.
About MRX1
MRX1 is an oil based, orally
administered drug candidate which is to be used in two Phase 2
clinical trials, the first evaluating MRX1's efficacy in treating
Chemotherapy Induced Peripheral Neuropathy ("CIPN") and the second
study is evaluating efficacy and retention in endometriosis
patients. You can read more about the CIPN clinical trial
here
and more about the endometriosis clinical
trial here.
Melissa Sturgess, CEO of the Company, commented:
"This study represents a
significant milestone in MRX1's journey to market, providing us
with key data for MRX1's licensed drug development. Working with an
excellent company such as Southern Star Research is a reflection of
the high quality of work produced by the Ananda team.
Southern Star
Research's deep expertise in clinical research, particularly
in the field of cannabinoids, will complement our own capabilities
and accelerate the development of MRX1. We all look forward to
updating shareholders as we progress through the deliverables on
this project."
Dr.
David Lloyd, Managing Director of Southern Star Research Pty Ltd,
commented: "We are thrilled to be
collaborating with Ananda Developments on their Phase I
Pharmacokinetics study of their lead asset, MRX1, to be assessed in
Healthy Volunteers. Southern Star Research have extensive
experience in managing and executing Phase I clinical trials and
also clinical studies involving Cannabinoids such as Cannabidiol
(CBD). The therapeutic potential of CBD is still yet to be fully
discovered, and we hope that our collaboration with Ananda will
further support the advancement of MRX1 and the wider
acceptance of CBD as a therapeutic solution within mainstream
health. We have enjoyed our working collaboration with the Ananda
team to date and look forward to bringing their Phase I PK
study to life here in Australia."
Further updates will be provided to
shareholders as the study progresses.
To stay up to date with the latest
developments at Ananda, we encourage you to follow and join our
social media channels which are:
· Register at our Investor Hub: https://investors.anandadevelopments.com/s/a66906
· Instagram: https://instagram.com/anandadevelopments?igshid=YmMyMTA2M2Y=
· LinkedIn: https://www.linkedin.com/company/anadevelopments/
· Twitter: https://twitter.com/AnandaPlc
· Investor Meet Company: https://www.investormeetcompany.com/ananda-developments-plc/register-investor
-Ends-
The Directors of the Company accept
responsibility for the contents of this announcement.
For
more information please contact:
InvestorHub
Engage with us directly at Ananda
Developments Investor Hub
|
Sign up at https://investors.anandadevelopments.com/s/a66906
|
ANANDA DEVELOPMENTS PLC
Chief Executive Officer
Melissa Sturgess
Finance Director
Jeremy Sturgess-Smith
|
+44 (0)7463 686 497
ir@anandadevelopments.com
|
SP
ANGEL CORPORATE FINANCE LLP
Corporate Finance
Richard Morrison
Caroline Rowe
|
+44 (0)20 3470 0470
|
Corporate Broking
Abigail Wayne
Rob Rees
|
|
Yellow Jersey PR
Charles Goodwin
Zara McKinlay
|
+44 (0)20 3004 9512
|
About Ananda Developments
Ananda is an AQSE-listed life
sciences company focused on the research and clinical development
of therapies for a range of complex inflammatory pain
conditions.
For further information on the
Company visit https://anandadevelopments.com/
or sign up at https://investors.anandadevelopments.com/s/a66906.
https://investors.anandadevelopments.com/link/5Pm3Me