FDA lifts hold on smoking cessation trial
Released
Released
Announcement PDF
ASX / MEDIA ANNOUNCEMENT
29 January 2014
INVION LIMITED ANNOUNCES FDA HAS CLEARED THE PATH
FOR “SMOKING CESSATION” CLINICAL TRIAL
OF ORAL INV102 (NADOLOL)
Invion Limited (ASX: IVX) is pleased to announce that the US Food and Drug Administration (FDA) has
removed the clinical hold on Invion’s phase II ‘smoking cessation’ clinical trial of INV102 (nadolol) in
patients with pre-existing chronic obstructive pulmonary disease (COPD).
On 20 December 2013, Invion announced that the FDA had requested changes to the ‘smoking
cessation’ clinical trial protocol that resulted in a halt to enrolment (clinical hold). Subsequent to
Invion’s prompt and full response to FDA requests, the Division of Anesthesia, Analgesia and Addiction
Products (DAAAP) accepted Invion’s amendments and has lifted the clinical hold.
While the changes were sufficient to require a re-launch of this study, Invion has expanded the number
of sites to minimise the impact on timing and reporting. New sites have been selected for their expertise
in smoking cessation, COPD, and analysis capabilities of biochemical markers of inflammation and
healing.
Invion Chief Medical Officer, Dr Mitchell Glass said, “The FDA took the unusual step of changing our
reviewing division to DAAAP after study initiation, which then placed us on clinical hold. Questions
raised by the DAAAP were resolved by aligning titration criteria and dosing with our asthma study.
These changes will enable sites to recruit and treat our targeted COPD patient population which is in
dire need of successfully quitting smoking.”
About Invion Limited
Invion is a life sciences company focussed on the development of treatments for major opportunities in
respiratory disease and autoimmune disease. The Group has three drug assets in development, and
three phase II clinical trials, regulated by the Food & Drug Administration (FDA), currently underway in
the United States. INV102 (nadolol) a beta blocker (beta adrenergic inverse agonist) currently used to
treat high blood pressure and migraine, is being repurposed to treat chronic inflammatory airway
diseases, including asthma and chronic obstructive pulmonary disease (COPD). INV104 (zafirlukast) is a
leukotriene receptor antagonist (LTRA) or anti-leukotriene that reduces inflammation, constriction of the
airways, and the build-up of mucus in the lungs. INV103 (ala-Cpn10) is a modified, naturally occurring
human protein which has been proposed as a founding member of the Resolution Associated
Molecular Pattern (RAMPs) family hypothesised to maintain and restore immune homeostasis. Invion is
an ASX listed company (ASX:IVX), with operations in Brisbane, Australia and Delaware, USA.
FOR MORE INFORMATION CONTACT
Managing Director and CEO: Dr Greg Collier. P: 07 3295 0506 investor@inviongroup.com
Media/ IR: Jane Lowe, Buchan Consulting P: 02 9237 2800 jlowe@buchanwe.com.au
Invion Limited ABN 76 094 730 417
GPO Box 1557, Brisbane, QLD, 4001. P +61 7 3295 0500 F +61 7 3295 0599 www.inviongroup.com
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