Teva Homepage Print this page Site Map
אודוΧͺ Χ˜Χ‘Χ’Χ§Χ©Χ¨Χ™ ΧžΧ©Χ§Χ™Χ’Χ™ΧΧžΧ’Χ•Χ¨Χ‘Χ•Χͺ Χ—Χ‘Χ¨ΧͺΧ™Χͺ

ηγωεϊ εδεγςεϊ μςιϊεπεϊ

ξθετμιν ιελμε μΰηρο αθξτψθεψϊ δηγψ ξζψχι χετχρεο ξελπιν μωιξεω ςγ ηεγω ιξιν δΰψλϊ ϊχετϊ δΰηρεο ξ-7 μςγ ηεγω ιξιν ϊΰτωψ πεηεϊ ψαδ ιεϊψ μηεμι θψωϊ πτεφδ αωμα δδϊχτι (RRMS) - αςιχψ μΰμε ωςαεγϊν ξηιιαϊ πιιγεϊ ψαδ

06/06/2007 θας ϊςωιεϊ τψξφαθιεϊ ας"ξ (πΰργ"χ: TEVA) ερπετι-ΰεεπθιρ ξεγιςεϊ διεν, λι ΰεωψδ δαχωδ μδΰψλϊ ϊχετϊ δΰηρεο αθξτψθεψϊ δηγψ ωμ ξζψχι χετχρεο (Glatiramer acetate μδζψχδ) ξελπιν μωιξεω, ξϊχετδ ωμ 7 ιξιν μϊχετδ ωμ ςγ ηεγω ιξιν. δΰιωεψ πιϊο δο ςμ ιγι ψωεϊ δξζεο εδϊψετεϊ δΰξψιχΰιϊ (δ-FDA) εδο αξγιπεϊ ΰιψετδ, αϊδμικ ΰιωεψ ψιωεν ξωεϊσ (MRP). δΰψλϊ δϊχετδ δξεϊψϊ μΰηρεο αθξτψθεψϊ δηγψ, ϊΰτωψ πεηεϊ ψαδ ιεϊψ μηεμι θψωϊ πτεφδ αωμα δδϊχτι (RRMS) - αςιχψ μΰμε δπςγψιν μϊχετεϊ ΰψελεϊ ξαιϊν.

β. ξφτεο δΰψυ, ξθετμϊ αχετχρεο ξςμ 8 ωπιν:"δςεαγδ ωΰελμ μδψωεϊ μςφξι μπρες' γαψ ωΰπι ςεωδ μςιϊιν χψεαεϊ, αΰψυ εμηε"μ αμι φιγπιϊ μωξιψϊ δϊψετδ αχιψεψ ϊχμ ςμι ξΰγ εϊωπδ μι ΰϊ δηιιν."

λψιρθιπδ ΰ., ζξψϊ ΰετψδ βψξπιδ δξθετμϊ αχετχρεο ξζδ 6 ωπιν, ξςιγδ: "λΰξπιϊ, ΰπι ξαμδ ζξο ψα αγψλιν, αξδμκ ριαεαι δετςεϊ. λςϊ, ιδιδ χμ επεη ιεϊψ μωΰϊ εμΰηρο ΰϊ ξζψχι δχετχρεο δξωξωιν ΰεϊι".

μεψδ χ., ξξωϊϊτεϊ δπιρει δψΰωεο αχετχρεο, ξεριτδ: "αξδμκ 15 δωπδ δΰηψεπεϊ, ΰπι ιλεμδ μωμεθ αξημδ εμχιιν ΰεψη ηιιν τςιμ εξμΰ, αζλεϊ δχετχρεο. λψελαϊ αϊηψειεϊ ρεριν, ΰπι πςγψϊ ξαιϊι μϊχετεϊ ξξεωλεϊ. δςεαγδ λι πιϊο μΰηρο ΰϊ δχετχρεο μξωκ ζξο ξξεωκ ιεϊψ αθξτψθεψϊ δηγψ, ϊδεεδ ςαεψι δχμδ ξωξςεϊιϊ".

ΰεγεϊ χετχρεο χετχρεο ξεϊεεδ μδτηϊϊ ϊγιψεϊ δδϊχτιν αηεμι θψωϊ πτεφδ αωμα δδϊχτι (RRMS), ωηεε ωπι δϊχτιν ΰε ιεϊψ ωμ ΰι-ργιψεϊ πειψεμεβιϊ, αξδμκ δωπϊιιν δΰηψεπεϊ. ξθετμι χετχρεο 20 ξ"β πγψωιν μδζψχδ ϊεκ εψιγιϊ ΰηϊ μιεν. δξιγς δξτεψθ μςιμ ΰιπε ξςγλο ΰϊ διγς δχιιν ΰεγεϊ ιςιμεϊ εραιμεϊ δχετχρεο, λτι ωπρχψ αςμεο μψετΰ.

χετχρεο® ξΰεωψ α-47 ξγιπεϊ αψηαι δςεμν, λεμμ ΰψδ"α, χπγδ, ξλριχε, ΰερθψμιδ, ιωψΰμ ελμ δξγιπεϊ δΰιψετΰιεϊ. χετχρεο ξωεεχ αΰιψετδ ςμ ιγι δηαψεϊ θας ϊςωιεϊ τψξφαθιεϊ ας"ξ ε-Sanofi-Aventis; εαφτεο ΰξψιχδ ςμ ιγι ηαψϊ Teva Neuroscience Inc., ηαψδ-αϊ ωμ θας ϊςωιεϊ τψξφαθιεϊ ας"ξ. χετχρεο διπε ριξο ξρηψι ψωεν ωμ θας ϊςωιεϊ τψξφαθιεϊ ας"ξ. θας ϊςωιεϊ τψξφαθιεϊ ας"ξ διπδ ηαψδ βμεαμιϊ ωαριρδ αιωψΰμ εΰηϊ ξ- 20 δηαψεϊ δτψξφαθιεϊ δξεαιμεϊ αςεμν. θας, δξϊξηδ αιιφεψ ϊψετεϊ βπψιεϊ ειιηεγιεϊ, ιιφεψ ηεξψιν τςιμιν μϊςωιδ δτψξφαθιϊ εξεφψιν εεθψιπψιν, διπδ δηαψδ δξεαιμδ αςεμν αϊηεν δβπψιχδ. μθας ΰϊψι ιιφεψ, ξηχψ, ωιεεχ εδτφδ αιωψΰμ, αφτεο εαξψλζ ΰξψιχδ εαΰιψετδ. ιεϊψ ξ- 76% ξξλιψεϊιδ ωμ δχαεφδ δο μφτεο ΰξψιχδ εΰιψετδ.



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 management’s current beliefs and expectations and involve a number of known and unknown risks and uncertainties that could cause Teva’s 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, Teva’s 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 Teva’s 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.