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

ϊεφΰεϊ ξηχψ ΰψεκ-θεεη αχετχρεο® ξρτχεϊ ηιζεχ περσ μπϊεπι διςιμεϊ εδαθιηεϊ
ωμ δϊλωιψ αθιτεμ αηεμι θψωϊ πτεφδ

25/02/2010
- μξςμδ ξ- 80% ξο δξθετμιν ξρεβμιν μμλϊ μμΰ ριες μΰηψ 15 ωπεϊ θιτεμ αχετχρεο® εξξεφς ωμ 22 ωπεϊ ξημδ.
- ψεα δηεμιν ξψΰιν ιφιαεϊ ΰε ωιτεψ αωιςεψ δξεβαμεϊ δτιζιϊ, λξε βν ιψιγδ ωμ 78% αωιςεψ δδϊχτιν δωπϊι (ARR)
  αδωεεΰδ μπϊεπι δαριρ.
- ξξφΰι δξηχψ ΰσ ξρτχιν ηιζεχ περσ μτψετιμ δαθιηεϊ ΰψεκ δθεεη δξιεηρ μχετχρεο®.

θας δεγιςδ διεν ςμ τψρεν ξξφΰιν ξξηχψ χμιπι ωπξωκ 15 ωπιν. ξηχψ τψερτχθιαι ζδ διπε δξηχψ δξξεωκ αιεϊψ ΰωψ αεφς ςγ λδ αχψα ηεμιν αθψωϊ πτεφδ αωμα δδϊχτι (Relapsing-remitting multiple sclerosis). δπϊεπιν τεψρξε αβιμιεο ηεγω ταψεΰψ ωμ διψηεο Multiple Sclerosis.

ξξφΰι δξηχψ ξφαιςιν ςμ λκ ωιεϊψ ξ-80% ξδηεμιν ξρεβμιν μμλϊ μμΰ ριες ςμ ΰσ ξωκ ζξο ξημδ ωμ 22 ωπιν. λωπι ωμιω ξδηεμιν ΰσ μΰ ςαψε μωμα δωπι δξϊχγν ωμ δξημδ. ξπιϊεη ϊεφΰεϊ δξηχψ ςεμδ λι ηεμιν ΰωψ πωΰψε αξηχψ ξςμ 15 ωπιν αξξεφς, δψΰε ιψιγδ αωιςεψ δδϊχτιν δωπϊι (ARR) αδωεεΰδ μπϊεπι δαριρ. λξε λο διϊδ ςμιδ ξιπιξμιϊ αγιψεβ δξεβαμεϊ δτιριϊ (Expanded Disability Status Scale). αξξεφς, ωιςεψ δδϊχτιν δωπϊι (ARR) ωμ δχαεφδ ιψγ ξψξδ ωμ 1.12 ± 0.82 μ- 0.25 ± 0.34 .

ξξφΰι δξηχψ ΰσ ξρτχιν ηιζεχ περσ μτψετιμ δαθιηεϊ ΰψεκ δθεεη δξιεηρ μχετχρεο®. ϊετςεϊ δμεεΰι δπτεφεϊ αιεϊψ ωπιφτε διε ϊβεαεϊ ξχεξιεϊ εξιιγιεϊ αΰζεψ δδζψχδ. μΰ πφτε δτψςεϊ ατςιμεϊ ξςψλϊ δηιρεο (immune-mediated disorders), ΰε ζιδεξιν εβιγεμιν.

"ξγεαψ αξιγς αςμ ηωιαεϊ βαεδδ μχδιμϊ δξθτμιν εδξθετμιν αθψωϊ πτεφδ, ωλο δεΰ ωα εξΰωω ΰϊ δϊεςμϊ δξεωβϊ αθιτεμ ΰψεκ-θεεη αχετχρεο® εΰϊ ιςιμεϊ δθιτεμ αδΰθϊ δϊχγξεϊδ δθαςιϊ ωμ δξημδ," ΰξψ τψετ' χεψι τεψγ, ηεχψ ψΰωι αξηχψ εξπδμ δξψτΰδ μθψωϊ πτεφδ ξΰεπιαψριθϊ πιε ξχριχε ωαΰψδ"α. "ζδ ξςεγγ μψΰεϊ ϊεφΰεϊ ΰψελεϊ-θεεη λΰμε ΰωψ ϊεξλεϊ αΰετο πηψυ αιηρ δϊεςμϊ-ριλεο ωμ θιτεμ ζδ δπιϊο μξημδ λψεπιϊ."

"ΰπηπε ωαςι ψφεο ξξξφΰι δξηχψ δξρτχιν ξωπδ ϊεχσ μπϊεπι διςιμεϊ εδαθιηεϊ δξεληιν ωμ χετχρεο® αθιτεμ ΰψεκ θεεη", ΰξψ ξωδ ξπεψ , ρξπλ"μ αλιψ μτιϊεη ξεφψιν ιιηεγιιν αθας. "ξηχψ ζδ ΰσ ωα εξγβιν ΰϊ δωχςϊδ ωμ θας αχετχρεο® εΰϊ ξηειιαεϊιπε δξϊξωλϊ μωιτεψ ΰιλεϊ ηιιδν ωμ δηεμιν αθψωϊ πτεφδ."

ξηχψ τψερτχθιαι ζδ ϊελπο μων ξςχα ΰψεκ θεεη εδςψλδ ωμ δθιτεμ δΰιξεπε-ξεγεμθεψι αηεμιν αθψωϊ πτεφδ αωμα δδϊχτι (RRMS). δξηχψ πξωκ λαψ 19 ωπιν εδεΰψκ λςϊ μ-20 ωπιν αδρϊξκ ςμ δϊεφΰεϊ δηιεαιεϊ ωδεωβε ςγ λδ εαδϊηωα αφεψκ δχιιν ωμ χδιμϊ δξθτμιν εδξθετμιν αξξφΰιν ΰψελι θεεη ωμ θιτεμ αξημδ λψεπιϊ ζε.

ΰεγεϊ δξηχψ
δξηχψ "θιτεμ ΰιξεπε-ξεγεμθεψι ξϊξωκ εΰψεκ-θεεη αθψωϊ πτεφδ: ϊεφΰεϊ ξπιϊεη 15 ωπεϊ ξηχψ τψερτχθιαι, βμει ϊεειεϊ ,ωπςψκ αΰψδ"α μθιτεμ α-glatiramer acetate", πςψκ αδξωκ μπιρει ωμα III ςιχψι . αξηχψ δωϊϊτε 100 ηεμιν ωθετμε αχετχρεο® δημ ξωπϊ 1991. ξφαν δεςψκ αΰξφςεϊ ρεμν δ- EDSS λμ ωιωδ ηεγωιν. ςμιιδ ωμ 1.0≤ αφιεο δ- EDSS μΰεψκ ωιωδ ηεγωιν πηωαδ λδψςδ αψξϊ δξεβαμεϊ δτιζιϊ, αςεγ ωωιπει ωμ 0.5≥ πηωα λ"ιφια/ξωϊτψ". αξηχψ πΰρτε πϊεπιν ΰεγεϊ ωιςεψ δξθετμιν ΰωψ δβιςε μφιεπι ρσ ωμ 4, 6 ΰε 8 αρεμν δ-EDSS μΰεψκ δθιτεμ αχετχρεο®, λξε βν δςψλϊ ξωκ δζξο δηφιεπι μδβςδ μρτιν ΰμε, ωηεωαδ ςμ τι ωιθϊ χτμο-ξΰιψ (KM).

ξφαν ωμ 57% ξδηεμιν δεβγψ λ"ιφια/ξωϊτψ" αφιεο δ- EDSS, αςεγ 65% ςγιιο μΰ ςαψ μδβγψδ ωμ ηεμιν αωμα δωπι ωμ θψωϊ πτεφδ (Secondary-Progressive Multiple Sclerosis (SPMS. αχψα δξθετμιν ξχαεφϊ mITT, πξφΰ λι αξωκ δθιτεμ αχετχρεο® πψωξδ ιψιγδ ξ- 1.18+/-0.82 μ-0.43+/-0.58 δϊχτιν αωπδ.

ΰεγεϊ χετχρεο®
χετχρεο (Glatiramer acetate injection) ® ξεϊεεδ μδτηϊϊ ϊγιψεϊ δδϊχτιν αηεμι θψωϊ πτεφδ αωμα δδϊχτι (RRMS). 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-51 ξγιπεϊ αψηαι δςεμν, αδο ΰψδ"α, χπγδ, ξχριχε, ΰερθψμιδ, ιωψΰμ ελμ ξγιπεϊ ΰιψετδ. χετχρεο® ξωεεχ 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 θψωϊ πτεφδ
θψωϊ πτεφδ (MS) πηωαϊ μξημϊ δςφαιν δωλιηδ αιεϊψ αχψα ΰπωιν φςιψιν. ξεςψκ λι ιωπν μτηεϊ 400,000 ηεμι θψωϊ πτεφδ αΰψδ"α μαγδ εμξςμδ ξ-2 ξιμιεο ηεμιν αψηαι δςεμν. ζεδι ξημδ τψεβψριαιϊ ωμ ξςψλϊ δςφαιν δξψλζιϊ δτεβςϊ αξεη, αηεθ δωγψδ εαςφαι δψΰιιδ. δϊδμικ δςιχψι αθψωϊ πτεφδ δεΰ ΰιαεγ εδψρ δξιΰμιο, ωδεΰ δψχξδ δωεξπιϊ δξβπδ ςμ χφεϊ δςφαιν.

ΰεγεϊ θας
θας ϊςωιεϊ τψξφαθιεϊ ας"ξ διπδ ηαψδ βμεαμιϊ ωαριρδ αιωψΰμ εΰηϊ ξ-20 δηαψεϊ δτψξφαθιεϊ δξεαιμεϊ αςεμν. θας, δξϊξηδ αιιφεψ ϊψετεϊ βπψιεϊ ειιηεγιεϊ ειιφεψ ηεξψιν τςιμιν μϊςωιιδ δτψξφαθιϊ, διπδ δηαψδ δξεαιμδ αςεμν αϊηεν δβπψιχδ. μθας ΰϊψι ιιφεψ, ξηχψ, ωιεεχ εδτφδ αιωψΰμ, αφτεο εαξψλζ ΰξψιχδ εαΰιψετδ. ιεϊψ ξ-80% ξξλιψεϊιδ ωμ δχαεφδ δο μφτεο ΰξψιχδ εΰιψετδ.

Teva’s 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 our 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: our ability to successfully develop and commercialize additional pharmaceutical products, the introduction of competing generic equivalents, the extent to which we may obtain U.S. market exclusivity for certain of our new generic products and regulatory changes that may prevent us 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 Neurontin®, Lotrel®, Protonix® and Eloxatin®, the current economic conditions, 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 effects of competition on our innovative products, especially Copaxone® sales, dependence on the effectiveness of our patents and other protections for innovative products, the impact of consolidation of our distributors and customers, the impact of pharmaceutical industry regulation and pending legislation that could affect the pharmaceutical industry, our ability to achieve expected results through our innovative R&D efforts, the difficulty of predicting U.S. Food and Drug Administration, European Medicines Agency and other regulatory authority approvals, the uncertainty surrounding the legislative and regulatory pathway for the registration and approval of biotechnology-based products, the regulatory environment and changes in the health policies and structures of various countries, supply interruptions or delays that could result from the complex manufacturing of our products and our global supply chain, our ability to successfully identify, consummate and integrate acquisitions, the potential exposure to product liability claims to the extent not covered by insurance, our exposure to fluctuations in currency, exchange and interest rates, significant operations worldwide that may be adversely affected by terrorism, political or economical instability or major hostilities, our ability to enter into patent litigation settlements and the intensified scrutiny by the U.S. government, the termination or expiration of governmental programs and tax benefits, impairment of intangible assets and goodwill, environmental risks, and other factors that are discussed in this report and in our other filings with the U.S. Securities and Exchange Commission ("SEC").
=