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ηγωεϊ εδεγςεϊ μςιϊεπεϊ

θιτεμ ξεχγν λλμ δΰτωψ αχετχρεο® ξςλα δϊτϊηεϊ θψωϊ πτεφδ

πιϊεη ϊεφΰεϊ δαιπιιν ωμ δπιρει δχμιπι PreCISe δελιη ϊεφΰεϊ ξψωιξεϊ αιεϊψ ξαηιπϊ ιςιμεϊ δωιξεω αχετχρεο® αηεμιν ωμχε αδϊχσ χμιπι ψΰωεο εαςμι ριλεο βαεδ μτϊη θψωϊ πτεφδ. ϊεφΰεϊ ΰμδ ξΰτωψεϊ δτρχϊ δπιρει ςτ"ι δλμμιν ωδεβγψε ξψΰω. θας ξϊλππϊ μδβιω αχωδ μΰιωεψι ωιεεχ ωμ χετχρεο® μθιτεμ αηεμιν ΰωψ μχε αδϊχσ χμιπι ψΰωεο.

03/12/2007 θας ϊςωιεϊ τψξφαθιεϊ ας"ξ (πργΰ"χ: TEVA) δεγιςδ διεν ςμ ϊεφΰεϊ ηιεαιεϊ απιϊεη δαιπιιν ωϊελπο ξψΰω αξηχψ δ-PreCISe, ωαεφς αηεμιν ΰωψ μχε αδϊχσ χμιπι ψΰωεο εδψΰε ρξξπιν δξψξζιν ςμ θψωϊ πτεφδ ααγιχϊ MRI. ξϊεφΰεϊ δαιπιιν ςεμδ, λι θιτεμ ξεχγν αϊψετϊ χετχρεο® (glatiramer acetate injection) δτηιϊ ΰϊ δριλεο ωμ δϊτϊηεϊ ξημϊ δθψωϊ δπτεφδ (Clinically Definite MS- CDMS) α-44% (ιηρ ριλεο 0.56, p=0.0005), διςγ δψΰωεπι ωμ δπιρει. δΰηεζεο δ-25 ωμ ξωκ δζξο ςγ δξςαψ μ-CDMS δεΰψκ ςμ ιγι δθιτεμ αχετχρεο® α-386 ιεν (115% (+, μ-722 ιξιν ξ-336 ιξιν αχαεφϊ δαιχεψϊ δτμριαε. μΰεψκ ϊχετϊ δξηχψ ςγ μπιϊεη δαιπιιν, δτηιϊ δθιτεμ αχετχρεο® ΰϊ ωιςεψ δξθετμιν ωΰεαηπε ληεμι CDMS ξ-43% αχψα χαεφϊ δαιχεψϊ , μ-25% αμαγ αχαεφϊ δξθετμιν αχετχρεο® (p<0.0001). θας ξϊλππϊ μδβιω αχωδ μΰιωεψι ωιεεχ ωμ χετχρεο® μθιτεμ αηεμιν ΰωψ μχε αδϊχσ χμιπι ψΰωεο δξψξζ ςμ θψωϊ πτεφδ, αΰιψετδ, αΰψδ"α εαχπγδ.

τψετ' τεμ ΰεχεπεψ, ψΰω δξημχδ δπειψεμεβιϊ ααιϊ δηεμιν ρπθ ξιιχμ αθεψεπθε, χπγδ, ειε"ψ δξεςφδ δςφξΰιϊ μπιθεψ πϊεπιν (DMC), ωτιχηδ ςμ δξηχψ, ΰξψ: "ΰπηπε ξϊψωξιν ξΰεγ ξξηειαεϊδ ωμ θας μδξωικ εμτϊη ΰϊ δχετχρεο® μξςο ηεμιν ΰωψ μχε αδϊχσ χμιπι ψΰωεο εδψΰε ρξξπιν ωμ θψωϊ πτεφδ ααγιχϊ MRI. δξεςφδ ξξμιφδ ωδξηχψ ιετρχ, αςχαεϊ δωβϊ πχεγϊ διςγ δψΰωεπιϊ ωδελιηδ ΰϊ ιςιμεϊ δθιτεμ αχετχρεο® ςμ τπι ξϊο τμριαε - ελμ δηεμιν ιεςαψε μθιτεμ τςιμ αχετχρεο® μξωκ ωπϊιιν περτεϊ".
ξηχψ ζδ, ξξωικ μδγβιν ΰϊ ΰτχθιαιεϊ δθιτεμ δξεχγν αχετχρεο® ςμ τςιμεϊ δξημδ βν αωμαιδ δψΰωεπιν, λτι ωπφτδ δο αϊεφΰεϊ δχμιπιεϊ εδο ααγιχεϊ MRI. απερσ ςμ λκ, χετχρεο® διπδ δϊψετδ διηιγδ μθψωϊ πτεφδ αωμα δδϊχτι, δξψΰδ ϊεφΰεϊ τψερτχθιαιεϊ μθεεη δΰψεκ, εξηχψ δπξφΰ αςιφεξε ξφαις ςμ λκ ω-92% ξδξθετμιν ωδβιαε μϊψετδ, ξφμιηιν μμλϊ μμΰ ριες βν μΰηψ 10 ωπεϊ θιτεμ ε-18 ωπεϊ ξημδ.

τψετ' β'πχψμε χεξι, ξδξημχδ μπειψεμεβιδ αξλεο δξγςι ρο ψτΰμ αξιμΰπε, ΰιθμιδ, εδηεχψ δψΰωι αξηχψ, ΰξψ: "ΰπηπε ξΰεγ ξψεφιν ξδϊεφΰεϊ. δξιγς ωπφαψ ΰεγεϊ χετχρεο® ιωτψ ΰϊ ΰτωψειεϊ δθιτεμ δςεξγεϊ ατπι ηεμι θψωϊ πτεφδ. δϊεφΰεϊ ξγβιξεϊ ΰϊ ηωιαεϊ δθιτεμ δξεχγν αηεμιν, αλγι μρτχ ωμιθδ ξεχγξϊ εξδιψδ αδϊχγξεϊ δξθετμιν μθψωϊ πτεφδ ξεληϊ χμιπιϊ".

ξωδ ξπεψ, ρβο πωιΰ ξωΰαιν ιιηεγιιν αθας ϊςωιεϊ τψξφαθιεϊ ας"ξ, ΰξψ: "ϊεφΰεϊ δαιπιιν ωμ ξηχψ ζδ, δξγβιξεϊ ΰϊ δδβπδ ωμ δχετχρεο® ξτπι δϊτϊηεϊ ξημϊ δθψωϊ δπτεφδ, ιηγ ςν τψετιμ δαθιηεϊ εδξιγς ΰεγεϊ ιςιμεϊ εαθιηεϊ δθιτεμ αχετχρεο® αηεμι RRMS, ξφιαιν ΰϊ χετχρεο® λΰετφιδ θιτεμιϊ ιεφΰϊ ξο δλμμ δο ςαεψ ηεμιν ΰωψ μχε αδϊχσ χμιπι ψΰωεο εδψΰε ρξξπιν μθψωϊ πτεφδ ααγιχϊ MRI εδο ςαεψ ηεμι θψωϊ πτεφδ αωμα δδϊχτι".

ΰεγεϊ δξηχψ
ξηχψ δ-PreCISe διπε πιρει ωμα III ΰχψΰι, λτεμ ρξιεϊ, ψθψερτχθιαι, βμεαΰμι, ψα-ξψλζι, ωπςψκ αλ-100 ξψλζιν αΰψδ"α, ΰιψετδ, ΰψβπθιπδ, ιωψΰμ, ξγιπεϊ ρχπγιπαιδ, ΰερθψμιδ επιε ζιμπγ. δξηχψ ξχισ 481 ξθετμιν, ΰωψ μχε αδϊχσ χμιπι ιηιγ, δψΰε ρξξπιν δξψξζιν ςμ θψωϊ πτεφδ ααγιχϊ MRI. ημχν θετμε αχετχρεο® αξιπεο 20 ξ"β ξγι ιεν; εμημχν πιϊπδ ζψιχϊ τμριαε ξγι ιεν - ζΰϊ, αξωκ ςγ 36 ηεγωιν ΰε ςγ ϊιςεγ ωμ δϊχσ ωπι εΰαηεπν ληεμι θψωϊ πτεφδ ξεληϊ χμιπιϊ ( (CDMS. ξθετμιν ωΰεαηπε ληεμι CDMS δξωιλε αθιτεμ τςιμ αξρβψϊ δπιρει, μϊχετδ ωμ ωπϊιιν περτεϊ.
δςψλϊ διςιμεϊ δψΰωεπιϊ πχαςδ ςμ τι ξωκ δζξο ςγ ΰαηεο CDMS, αδϊαρρ ςμ δϊψηωεϊ ΰιψες χμιπι ωπι. πιϊεη δαιπιιν δξϊελπο ξψΰω, πωςο ςμ λ-80% ξπϊεπι δξηχψ αο ωμεω δωπιν,. μΰεψκ ϊχετϊ δξηχψ ςγ ξεςγ πιϊεη δαιπιιν, δτηιϊ δθιτεμ αχετχρεο® ΰϊ ωιςεψ δξθετμιν ωΰεαηπε ληεμι CDMS ξ-43% αχαεφϊ αχψϊ δτμριαε μ-25% αμαγ αχαεφϊ δξθετμιν αχετχρεο® (p<0.0001).
λξε λο, αξδμκ ξηχψ δ-PreCISe δεφβδ ραιμεϊ βαεδδ μχετχρεο®, ςν ωιςεψ πωιψδ ωμ 13% αμαγ μΰεψκ ωμεω ωπεϊ δπιρει. λμ ξωϊϊτι δπιρει ξωϊϊτιν βν αξηχψ δξωκ μδςψλδ τψερτχθιαιϊ ωμ θιτεμ ξεχγν ξεμ ξΰεηψ αχετχρεο® αξδμλδ δξξεωκ ωμ δξημδ, μΰεψκ θεεη ζξο λεμμ ωμ ςγ ηξω ωπιν.

ΰεγεϊ θας
θας ϊςωιεϊ τψξφαθιεϊ ας"ξ (πργΰ"χ: TEVA) 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. χψεα μ-80% 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:

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 extent to which Teva may obtain U.S. market exclusivity for certain of its new generic products and regulatory changes that may prevent Teva from utilizing exclusivity periods, competition from brand-name companies that are under increased pressure to counter generic products, or competitors that seek to delay the introduction of generic products, the impact of consolidation of our distributors and customers, 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®, Lotrel® and Famvir®, 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, our ability to achieve expected results though our innovative R&D efforts, Teva’s ability to successfully identify, consummate and integrate acquisitions, potential exposure to product liability claims to the extent not covered by insurance, dependence on the 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, supply interruptions or delays that could result from the complex manufacturing of our products and our global supply chain, environmental risks, fluctuations in currency, exchange and interest rates, 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.