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ηγωεϊ εδεγςεϊ μςιϊεπεϊξηχψ ηγω περσ ξφαις ςμ ιςιμεϊε δβαεδδ ωμ δχετχρεο βν αθιτεμ αηεμιν ωςαψε ξθιτεμ αΰιπθψτψεο αθΰχετχρεο ωμ θας ξτηιϊδ ξωξςεϊιϊ ΰϊ τςιμεϊ δξημδ αχψα ηεμι θψωϊ πτεφδ αωμα δδϊχτι (RRMS), ωςαψε ξωιξεω αΰιπθψτψεο αθΰ (IFNb) ςχα δϊτϊηεϊ πεβγπιν ξπθψμιν (NAbs)23/10/2007 ξηχψ δωεεΰϊι ψθψερτχθιαι ξφΰ δΰψλδ ξωξςεϊιϊ ωμ τψχ δζξο ςγ δδϊχσ δψΰωεο (p=0.0389) αχψα ηεμι θψωϊ πτεφδ αωμα δδϊχτι (RRMS), ωςαψε μθιτεμ αχετχρεο ωμ θας μΰηψ ωθετμε αΰιπθψτψεο αθΰ ετιϊηε ιψιγδ αιςιμεϊ δθιτεμ ςχα δϊτϊηεϊ πεβγπιν ξπθψμιν (NAbs). ςεγ πξφΰδ ιψιγδ αωιςεψ δδϊχτιν δωπϊι δξξεφς αχψα ηεμιν ωδεςαψε μθιτεμ αχετχρεο, αδωεεΰδ μϊχετδ δχεγξϊ μθιτεμ αΰιπθψτψεο αθΰ. ϊεφΰεϊ δξηχψ δεφβε αχεπβψρ δ-23 ωμ ECTRIMS (δεεςιγδ δΰιψετιϊ μθιτεμ εξηχψ αθψωϊ πτεφδ) ωπςψκ αωαες ωςαψ ατψΰβ, φ'λιδ."ςγ 30% ξηεμι δ-RRMS δξθετμιν αϊλωιψι δΰιπθψτψεο αθΰ, ςωειιν μτϊη πεβγπιν ξπθψμιν ΰωψ ξτηιϊιν ΰϊ ιςιμεϊ δθιτεμ", ξρψ γ"ψ ΰπθεπιε αψθεμεθε, ψετΰ ξεξηδ εηεχψ θψωϊ πτεφδ ξαιϊ δηεμιν δΰεπιαψριθΰι ρο μεΰιβ'ι, αΰεψαρΰπε, ΰιθμιδ. "αξψλζ δψτεΰι ωμπε μθιτεμ αθψωϊ πτεφδ, δςαψπε μθιτεμ αχετχρεο ηεμιν ΰωψ θετμε αΰιθψτψεο-αθΰ, τιϊηε πεβγπιν ξπθψμιν, ωαθμε ΰϊ δτςιμεϊ δαιεμεβιϊ ωμ δΰιπθψτψεο αθΰ λτι ωπξφΰ ααγιχεϊ MxA ε-mRNA, εραμε αξξεφς ξδϊχσ ΰηγ μτηεϊ αωπδ. δπϊεπιν ωΰρτπε ξψΰιν, λι ςμ δψετΰιν μδτριχ μθτμ αΰιπθψτψεο αθΰ αηεμιν ωτιϊηε πεβγπιν ξπθψμιν - ελι ςμιδν μωχεμ αηιεα δςαψϊ ηεμιν ΰμε μθιτεμ αχετχρεο ΰωψ ξφμιη μδτηιϊ ΰϊ δϊχγξεϊ δξημδ". ΰεγεϊ δξηχψ αξρβψϊ δξηχψ δδωεεΰϊι δψθψερτχθιαι δεςψλε δδαγμιν αιο θιτεμ αχετχρεο μαιο θιτεμ αΰιπθψτψεο αθΰ, αδϊιιηρεϊ μπϊεπι ωιςεψ δδϊχτιν δωπϊι, ωιςεψ δηεμιν ωμΰ ηεε δϊχτιν λμμ εξωκ δϊχετδ ςγ δδϊχσ δψΰωεο. δξηχψ πςψκ αχψα 19 ηεμιν ωθετμε αΰιπθψτψεο αθΰ εδεςαψε μθιτεμ αχετχρεο, μΰηψ ωτιϊηε πεβγπιν ξπθψμιν. δηεμιν ωδωϊϊτε απιρει ΰεαηπε αΰετο ςχαι λαςμι πεβγπιν ξπθψμιν (μτηεϊ ηεγωιιν αψφιτεϊ); μΰ δψΰε τςιμεϊ αιεμεβιϊ ωμ δΰιπθψτψεο αθΰ ααγιχεϊ MxA ε-mRNA; πΰξγδ ΰφμν τςιμεϊ πξελδ ωμ δξημδ μΰεψκ δθιτεμ αΰιπθψτψεο αθΰ (δϊχσ ΰηγ ΰε τηεϊ αωπδ δΰηψεπδ μθιτεμ αΰιπθψτψεο αθΰ); εδν θετμε αχετχρεο μτηεϊ 12 ηεγωιν μΰηψ ωδεςαψε μϊψετδ ζε. ωιςεψ δδϊχτιν δωπϊι δξξεφς παγχ θψν ϊηιμϊ δθιτεμ αΰιπθψτψεο αθΰ; μΰεψκ δθιτεμ αΰιπθψτψεο αθΰ, θψν δϊτϊηεϊ δπεβγπιν δξςλαιν; μΰεψκ δθιτεμ αΰιπθψτψεο αθΰ, μΰηψ δετςϊ δπεβγπιν δξςλαιν; εμΰηψ ϊηιμϊ δθιτεμ αχετχρεο (glatiramer actate injection) - επξφΰε δπϊεπιν δαΰιν, αδϊΰξδ: 0.98, 0.1, 0.32 ε-0.21 (p<0.001 θψν ϊχετϊ δθιτεμ αΰιπθψτψεο αθΰ αδωεεΰδ μλμ ΰηϊ ξϊχετεϊ δαγιχδ δπερτεϊ; p=NS μλμ πιϊεη χαεφϊι ΰηψ). πξφΰε δαγμιν ξωξςεϊιιν αξωκ δϊχετδ ςγ δδϊχσ δψΰωεο αιο δθιτεμ αΰιπθψτψεο αθΰ θψν δϊτϊηεϊ δπεβγπιν δξςλαιν, δθιτεμ αΰιπθψτψεο αθΰ μΰηψ δϊτϊηεϊ δπεβγπιν δξςλαιν εδθιτεμ αχετχρεο - ςν δαγμ αψεψ αιο δθιτεμ αΰιπθψτψεο αθΰ μΰηψ δϊτϊηεϊ δπεβγπιν δξςλαιν μθιτεμ αχετχρεο (δΰηεζεο δ-50: 17.8 ηεγωιν μςεξϊ 37.9 ηεγωιν; ΰηεζεο 75: 6.9 ηεγωιν μςεξϊ 12.9 ηεγωιν; p=0.0389). ξιγς περσ ΰεγεϊ ωιθϊ δξηχψ εϊεφΰεϊιε, πιϊο μχαμ ατερθψ: Glatiramer acetate reduces disease activity in NAbs to IFNb-positive patients, by M. Capobianco, A. Sala, S. Malucchi, M. Caldano, A. Di Sapio, F. Sperli, A. Oggero, F. Marnetto, P. Valentino, L. Granieri, F. Gilli, A. Bertolotto. ΰεγεϊ θψωϊ πτεφδ θψωϊ πτεφδ (MS) πηωαϊ μξημϊ δςφαιν δωλιηδ αιεϊψ αχψα ΰπωιν φςιψιν. ξεςψκ λι ιωπν λ-400,000 ηεμι θψωϊ πτεφδ αΰψδ"α μαγδ, εμξςμδ ξξιμιεο ηεμιν αψηαι δςεμν. ζεδι ξημδ γξιιμιπθιαιϊ τψεβψριαιϊ ωμ ξςψλϊ δςφαιν δξψλζιϊ, δεβςϊ αξεη, αηεθ δωγψδ εαςφαι δψΰιιδ. ηεμι θψωϊ πτεφδ ςμεμιν μηεεϊ ριξτθεξιν τιριιν ε/ΰε χεβπθιαιιν, δλεμμιν ηεμωδ, ςιιτεϊ, πιεεο ωψιψιν, ϊτχεγ μχει, αςιεϊ αωμτεηιϊ ωϊο εαξςι δβρ εδωτςδ ςμ δηεωιν εςμ δψΰιιδ. λξε λο, μξημδ δωτςδ ξωξςεϊιϊ ςμ δϊτχεγ δρεφιΰμι εςμ ΰιλεϊ δηιιν ωμ δηεμιν. ΰεγεϊ χετχρεο® χετχρεο® (Glatiramer acetate injection) ξεϊεεδ μδτηϊϊ ϊγιψεϊ δδϊχτιν αηεμι θψωϊ πτεφδ αωμα δδϊχτι. ϊετςεϊ δμεεΰι δπτεφεϊ αιεϊψ ωμ χετχρεο® δο ΰγξεξιεϊ, λΰα, πτιηεϊ, βιψεγ ΰε βεω αξχεν δδζψχδ, ηεμωδ, ζιδεν, αηιμδ, λΰα τψχιν, ηψγδ επεχωεϊ δωψιψιν. δωιξεω αχετχρεο® ξΰεωψ λιεν α-48 ξγιπεϊ αψηαι δςεμν, αδο ΰψδ"α, χπγδ, ξχριχε, ΰερθψμιδ, ιωψΰμ ελμ ξγιπεϊ ΰιψετδ. χετχρεο® ξωεεχϊ αφτεο ΰψδ"α ςμ ιγι Teva Neuroscience Inc, ωδιΰ ηαψϊ αϊ ωμ θας ϊςωιεϊ τψξφαθιεϊ ας"ξ; εαΰιψετδ ςμ ιγι θας ϊςωιεϊ τψξφαθιεϊ ας"ξ ε-Sanofi-Aventis. χετχρεο® δεΰ ριξο ψωεν ωμ θας ϊςωιεϊ τψξφαθιεϊ ας"ξ. ΰεγεϊ θας θας ϊςωιεϊ τψξφαθιεϊ ας"ξ διπδ ηαψδ βμεαμιϊ ωαριρδ αιωψΰμ, ΰηϊ ξ-20 ηαψεϊ δτψξφαθιχδ δξεαιμεϊ αςεμν εδηαψδ δβπψιϊ δξεαιμδ. θας ξϊξηδ ατιϊεη, ιιφεψ εωιεεχ ϊψετεϊ βπψιεϊ ειιηεγιεϊ, ηεξψιν τςιμιν μϊςωιιδ δτψξφαθιϊ εξεφψιν εεθψιπψιν. χψεα μ-75% ξξλιψεϊ δχαεφδ ξψελζεϊ αφτεο ΰξψιχδ εαΰιψετδ. τςιμειεϊ δξε"τ ωμ θας ξϊξχγεϊ ατιϊεη ϊψετεϊ ςαεψ ξημεϊ δτεβςεϊ δξςψλϊ δςφαιν δξψλζιϊ. μδμο δρςισ διγες αΰψδ"α λ- Safe Harbor απερηε δΰπβμι εΰωψ ξθψϊε μδβο ςμ δηαψδ, ςτ"ι δγιο δΰξψιχΰι: Safe Harbor Statement under the U. S. Private Securities Litigation Reform Act of 1995: This release contains forward-looking statements, which express the current beliefs and expectations of management. Such statements are based on managements current beliefs and expectations and involve a number of known and unknown risks and uncertainties that could cause Tevas future results, performance or achievements to differ significantly from the results, performance or achievements expressed or implied by such forward-looking statements. Important factors that could cause or contribute to such differences include risks relating to Teva`s ability to successfully develop and commercialize additional pharmaceutical products, the introduction of competing generic equivalents, the competition from brand-name companies that are under increased pressure to counter generic products, or competitors that seek to delay the introduction of generic product, Teva's ability to generate revenues and profits closely tied to our success in obtaining U.S. market exclusivity for generic products, the impact of consolidation of our distributors and customers, regulatory changes that may prevent Teva from utilizing exclusivity periods, potential liability for sales of generic products prior to a final resolution of outstanding patent litigation, including that relating to the generic versions of Allegra®, Neurontin® and Wellbutrin XL® , the effects of competition on our innovative products, especially Copaxone® sales, the impact of pharmaceutical industry regulation and pending legislation that could affect the pharmaceutical industry, the difficulty of predicting U.S. Food and Drug Administration, European Medicines Agency and other regulatory authority approvals, the regulatory environment and changes in the health policies and structures of various countries, Tevas ability to successfully identify, consummate and integrate acquisitions, potential exposure to product liability claims which are not covered by insurance, dependence on effectiveness of our patents and other protections for innovative products, significant operations worldwide that may be adversely affected by terrorism, political or economical instability or major hostilities, the difficulty of complex manufacturing of our products and supply delays, environmental risks, fluctuations in currency, exchange and interest rates, operating results and other factors that are discussed in Tevas Annual Report on Form 20-F and its other filings with the U.S. Securities and Exchange Commission. Forward-looking statements speak only as of the date on which they are made and the Company undertakes no obligation to update or revise any forward-looking statement, whether as a result of new information, future events or otherwise.
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