CAT appoints R&G Pharma as CRO for nadolol in China
Released
Released
Announcement PDF
ASX ANNOUNCEMENT
INVION SPIN-OFF CHRONIC AIRWAY THERAPEUTICS SELECTS LEADING CRO
FOR THE FUTURE DEVELOPMENT OF NADOLOL
Highlights
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Chronic Airway Therapeutics (CAT) selects R&G Pharma to progress Chinese
development of nadolol
R&G is one of China’s leading Contract Research Organisations
CAT, R&G ready to commence regulatory process and will request pre-IND meeting with
China Food and Drug Administration
Melbourne, Australia and Delaware, United States, 27 September 2018: Chronic Airway
Therapeutics (CAT), a proposed spin-off from Invion Limited (ASX: IVX, “Invion” or “Company”),
has selected leading Chinese contract research organisation R&G Pharma Studies Co., Ltd
to support the development in China of nadolol as a treatment for chronic obstructive
pulmonary disease (COPD).
R&G is one of China’s leading Contract Research Organisations (CROs) working closely with
multiple Centres of Excellence located throughout China. CAT selected R&G because of the
company’s demonstrated expertise, strong relationships with the China Food and Drug
Administration (CFDA), and deep understanding of the similarities and differences with
US FDA regulations.
CAT and R&G will focus their efforts towards lodging formal requests for a pre-IND and
End of Phase II meeting with the CFDA during the 4th quarter of 2018. The pre-IND meeting is a
crucial step towards commencing Phase III clinical trials in China, with a view to gaining
regulatory approval for the Chinese market.
Nadolol, which – unlike existing treatments – can be administered in one single tablet per day,
could play an integral role in diminishing the impact of COPD.
Dr Mitchell Glass, currently Invion’s Chief Medical Officer, and to be appointed as CAT executive
director, will lead CAT’s research and development program.
“This partnership with R&G provides increased confidence that our clinical studies will support
approval in China and be widely accepted scientifically,” Dr Glass said.
COPD, which is a major health problem in China, describes various long-term lung diseases that
cause shortness of breath. It includes emphysema and chronic bronchitis.
The prevalence of COPD in China is estimated to be above 50 million patients, and rising due to
the country’s serious air pollution and high rate of cigarette smoking. Chinese authorities have
identified COPD as a critical area of medical need.
Invion Limited ABN 76 094 730 417
722 High Street, East Kew, VIC 3102 Australia
P: +61 3 9081 6005 W: www.inviongroup.com
ASX ANNOUNCEMENT
Dr Mitchell Glass said, “The risk of COPD and its complications - including chronic cough,
increased sputum production, risk of hospitalisation and death - are all compounded by air
pollution, which is a serious issue in China.”
Invion announced earlier in September 2018 that it would demerge its two respiratory assets,
nadolol (INV102) and zafirlukast (IV104), into a separate company, Chronic Airway Therapeutics,
subject to shareholder approval at the company’s General Meeting to be held on
Tuesday 13 November 2018 in Melbourne.
Invion shareholders will be entitled to one CAT share for each Invion share they hold at the
record date of Friday 16 November 2018. Investors who acquire shares Invion shares before the
record date will be eligible to participate in CAT’s future development as a stand-alone
company and its progress in the significant China market.
The Cho Group of Hong Kong, the organisation that is funding the research and development of
Invion’s PhotosoftTM technology, will fund CAT’s initial overhead and operating costs to enable
the new company to establish a pathway with the CFDA.
About Invion
Invion is a clinical-stage life-sciences company that is leading the global clinical development of
the Photosoft™ technology for the treatment of cancers. Invion has been appointed exclusive
distributor and licensee in Australia and New Zealand of Photosoft™. The appointment has been
made by technology licensor, The Cho Group, a Hong Kong based group that has funded and
successfully commercialised a number of unique and advanced technologies. Via an R&D
services agreement between the two entities, the research and clinical trials of Photosoft™ are
funded by The Cho Group. Invion has an alliance with leading Australian medical research
institute, Hudson Institute of Medical Research, for the Photosoft™ research program.
About Photodynamic Therapy (PDT)
Invion is developing PhotosoftTM technology as an improved next-generation Photodynamic
Therapy. PDT uses non-toxic photosensitisers and visible light in combination with oxygen to
produce cytotoxic-reactive oxygen that kills malignant cells, shuts down tumours and stimulates
the immune system. In contrast to surgery, or radiotherapy and chemotherapy which are mostly
immunosuppressive, PDT causes acute inflammation, expression of heat-shock proteins, and
invasion and infiltration of a tumour by leukocytes.
____________________________________________
Investor enquiries
Managing Director & CEO, Dr Greg Collier
T: +61 3 9081 6005
E: investor@inviongroup.com
Invion Limited ABN 76 094 730 417
722 High Street, East Kew, VIC 3102 Australia
P: +61 3 9081 6005 W: www.inviongroup.com
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