End of Phase 2 Meeting for INV102 (nadolol)
Released
Released
Announcement PDF
ASX / MEDIA ANNOUNCEMENT
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INVION ANNOUNCES SUCCESSFUL MEETING WITH FDA TO PROGRESS DEVELOPMENT OF
INV102
Brisbane, Australia and Delaware, United States, 4 April 2016: Australian drug development company
Invion Limited (ASX:IVX) is pleased to advise that it has met with the Division of Anesthesia, Analgesia,
and Addiction Products (DAAAP) of the US Food and Drug Administration (FDA) to discuss Phase 3 plans
for development of oral nadolol as a treatment for patients with COPD who cannot quit cigarette
smoking.
Written and oral communication fully supports Invion’s proposals for further manufacturing in
conjunction with Phase 3 development. In addition, the FDA confirmed that the animal toxicology
package is complete. The Company and the FDA engaged in a highly productive dialogue on the
design and regulatory target of the Phase 3 plan for oral INV102. In meeting directly with senior FDA
officials, Invion team members were able to explain the role that airway healing can play in enabling
these patients to quit, by reducing cough and phlegm. Invion was able to place the smoking cessation
program into the context of treating COPD.
Executive Vice President R&D and Chief Medical Officer, Dr Mitchell Glass said, “We are pleased that
the FDA has confirmed our plans for INV102 as a treatment for patients with established chronic
bronchitis who cannot quit smoking due to increased cough and sputum production.
“Our discussion, based on their in-depth review, reflected their deep interest in our program and their
shared desire to see us succeed in enabling these patients to quit by ameliorating symptoms that have
precluded previous quit attempts.
“We welcome their recommendations, which will focus and strengthen our registration program without
causing delay.”
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FOR MORE INFORMATION CONTACT Dr Greg Collier. P: 07 3295 0500 greg.collier@inviongroup.com
About Invion Limited
Invion is a life sciences company focussed on the development of treatments for major opportunities in
respiratory and autoimmune disease. Invion has three drug assets in development across four
development programs. Invion is an ASX listed company (ASX:IVX), with operations in Brisbane, Australia
and Delaware, USA.
INV102 (nadolol) is a beta adrenergic biased ligand targeted to reverse mucous metaplasia in
the airway epithelium treat chronic inflammatory airway diseases. In Q4 2015, Invion reported
that data from a 155 patient phase 2 study of oral INV102 in smoking cessation demonstrated
good safety and that treated patients were more likely to stop smoking completely or
dramatically reduce the number of cigarettes smoked. An End of Phase 2 Meeting with the
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
ASX / MEDIA ANNOUNCEMENT
FDA was held in 1Q 2016. Feasibility for an inhaled version of the drug to potentially treat COPD
and cystic fibrosis is well-progressed with 3M Drug Delivery Systems, and toxicological studies
have commenced. In addition, a phase 2 study of oral INV102 in mild asthma patients funded
by the US NIH is fully recruited and will complete dosing in 1H 2016.
INV104 (zafirlukast) is a leukotriene receptor antagonist (LTRA) that reduces inflammation,
constriction of the airways, and the build-up of mucus in the lungs. An FDA-approved oral
therapy, Invion is, through a joint development and licensing agreement with Hovione Scientia
Limited, developing a proprietary dry powder formulation of the drug for the development of
INV104 (zafirlukast) as a potential inhaled therapy for asthma.
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 reported final data from its
phase 2 clinical trial in lupus patients in Q3 2015. 30mg and 100mg iv twice weekly showed
reduced response to stimulation by LPS after 1 month of dosing. These data, which reflect
relevant activity at the target cell type in patients with a target (autoimmune) disease, has
formed the foundation of partnering discussions for this program.
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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