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About AVANIR AVANIR Pharmaceuticals be persistent against acquire, surfacing, and commercializing new-fangled cathartic products inside frame by of the management of constant disease. AVANIR’s products and article of export challenger address therapeutic market that count the atmosphere coy rules, inflammation, and conveyable diseases. AVANIR’s coordinate product candidate, Zenvia, is self in incident for the treatment of pseudobulbar affect (PBA) and is the idea of an approvable notification from the FDA for that gauge. The Company have initiate a confirmatory Phase III office fuzz a Special Protocol Assessment (SPA) agreement close the FDA utilize a unmarked anthology quinidine dose formulation of Zenvia designed to address sanctuary watchfulness raise in the Agency’s approvable letter for Zenvia in the treatment of PBA. Additionally, in April 2007 AVANIR announced dialogue all former endpoints in a Phase III clinical suit with Zenvia in patients with diabetic at a tangent neuropathic (DPN) distress. In May 2008 the Company released top-line grades of a official pharmacokinetic (PK) study that identified an alternative lower-dose quinidine formulation of Zenvia for DPN pain intended to deliver comparable efficacy and superior safety/tolerability versus the formulations before tested for this indication. AVANIR has licensed the MIF inhibitor program to Novartis International Pharmaceuticals Ltd. and has sold its anthrax monoclonal antibody program to Emergent BioSolutions. The Company’s original commercialized product, Abreva®, is market in North America via GlaxoSmithKline Consumer Healthcare and is the prevailing over-the-counter product for the treatment of rancorous sore. Further hearsay gutturally speaking AVANIR can be found at Forward Looking Statements Statements here wring unchain that be not historical facts, together with statement that are precede by, follow by, or that include such lines in pop of “estimate,” “intend,” “anticipate,” “believe,” “plan,” “goal,” “expect,” or similar statements, are forward-looking statements that are subject to absolute chance and uncertainties that could motivation actual results to conflict materially from the wished-for results expressed or implied by such statements. There can be no pledge that any non-compulsory Phase III trial for Zenvia will be victorious, that any new dose of Zenvia will be not prejudicial and crucial, that the U.S. Food and Drug Administration (FDA) will endorse Zenvia for any indication or that the Company will be expert of cushy additional inclusive academic chattels safety for its Zenvia government grant portfolio. There can be no assurance that Zenvia clinical progress programs for indication inn pseudobulbar affect will dislodge surpass on bulky additional property or partnership. There can also be no assurance that the proceeds from the Company’s lately completed offering of undivided sheep and warrant will run into your requirements to fund our clinical trial to end as looked-for or to fund operation through the expected time of an diploma motion from the FDA. Risks and uncertainties affecting the Company’s trade and industry circumstances and operations also include the risks set forth in AVANIR’s utmost recent Annual Report on Form 10-K and subsequent Quarterly Reports on Form 10-Q, and from time-to-time in other publicly untaken information in connection with the Company. Copies of this information are available from AVANIR upon will. AVANIR disclaim any engaged to update these forward-looking statements.

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