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About AVANIR AVANIR Pharmaceuticals be penalizing next to acquire, budding, and commercializing fresh counteractive products in support of the exposure of persistent illness. AVANIR’s products and article of trade candidate address therapeutic market that involve the interior agitated arrangement, inflammation, and communicable diseases. AVANIR’s plan product candidate, Zenvia, is all and sundry power-driven for the treatment of pseudobulbar affect (PBA) and is the subject matter of an approvable notification from the FDA for that verification. The Company have initiate a confirmatory Phase III amend below a Special Protocol Assessment (SPA) agreement beside the FDA utilize a pour scorn on new discomfit quinidine dose formulation of Zenvia authentic to address refuge concern raise contained with the Agency’s approvable letter for Zenvia in the treatment of PBA. Additionally, in April 2007 AVANIR announced symposium all original endpoints in a Phase III clinical audible range with Zenvia in patients with diabetic divergent neuropathic (DPN) anguish. In May 2008 the Company released top-line grades of a formalized pharmacokinetic (PK) study that identified an alternative lower-dose quinidine formulation of Zenvia for DPN pain intended to deliver similar to efficacy and enhanced safety/tolerability versus the formulations past 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 first showing commercialized product, Abreva®, is souk in North America by GlaxoSmithKline Consumer Healthcare and is the chief over-the-counter product for the treatment of icy aching. Further data gratingly AVANIR can be found at Forward Looking Statements Statements here yank unfetter that be not historical facts, as capably as authentication that are precede by, follow by, or that include such lines in place of “estimate,” “intend,” “anticipate,” “believe,” “plan,” “goal,” “expect,” or similar statements, are forward-looking statements that are subject to certain risk and uncertainties that could produce actual results to be dissimilar materially from the impending results expressed or implied by such statements. There can be no warranty that any lower Phase III trial for Zenvia will be dominant, that any new dose of Zenvia will be risk-free and high-ranking, that the U.S. Food and Drug Administration (FDA) will be behind something Zenvia for any indication or that the Company will be competent to drop out of action additional collective analytical richness haven for its Zenvia rights portfolio. There can be no assurance that Zenvia clinical change for the better programs for indication excluding pseudobulbar affect will roam frontal minus additional profits or partnership. There can also be no assurance that the proceeds from the Company’s lately completed offering of established cattle and warrant will do to fund our clinical trial to end as appointed or to fund operation through the expected time of an glory judgment from the FDA. Risks and uncertainties affecting the Company’s trade and industry must and operations also include the risks coagulate forth in AVANIR’s peak recent Annual Report on Form 10-K and subsequent Quarterly Reports on Form 10-Q, and from time-to-time in other publicly going spare information concerning 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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