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ηγωεϊ εδεγςεϊ μςιϊεπεϊ

δημ βιερ δξθετμιν μπιρει ωμα 3 αϊψετϊ δ-Laquinimod μθιτεμ ΰεψΰμι αθψωϊ πτεφδ αωμα δδϊχτι

07/11/2007 θας ε- Active Biotech AB δωαγιϊ (OMX NORDIC: ACTI) δεγιςε διεν ςμ ϊηιμϊ ωμα βιερ ξθετμιν μπιρει δχμιπι Allegro - πιρει μδςψλϊ διςιμεϊ, δαθιηεϊ εδραιμεϊ αξϊο δϊλωιψ δΰεψΰμι Laquinimod αξπιςϊ δδϊχγξεϊ ωμ θψωϊ πτεφδ, αδωεεΰδ μξϊο τμριαε. Allegro, ξηχψ αωμα III ωμ δτιϊεη δχμιπι, διπε βμεαΰμι, λτεμ- ρξιεϊ ΰωψ ιΰψκ 24-30 ηεγωιν αχψα αηεμι θψωϊ πτεφδ αωμα δδϊχτι (RRMS). δξηχψ ωεΰσ μβιιρ λ-1,000 ηεμι RRMS. "λιεν ιωπν ξρτψ θιτεμιν μ-RRMS, ΰκ λεμν πιϊπιν ςμ ιγι ζψιχδ ΰε ςιψει. θιτεμ αξϊο ΰεψΰμι ξχγν ΰεϊπε φςγ περσ μχψΰϊ δΰτωψεϊ ωμ ψετΰιν εηεμιν μαηεψ αθιτεμ τηεϊ τεμωπι εΰτχθιαι ιεϊψ, ηγωπι επεη", ΰεξψ γΰβ β'τψι, τψετρεψ ηαψ αξψλζ δψτεΰι δατθιρθι ωμ ΰεπιαψριθϊ Wake Forest, εξερισ: "πιρειιν χεγξιν αωμα 2 ωμ δτιϊεη δχμιπι δγβιξε ϊεφΰεϊ ηιεαιεϊ μ-Laquinimod εΰπε ξχεειν ωϊεφΰεϊ δπιρει δξεψηα αωμα 3 ιηζχε ΰϊ δξξφΰιν δμμε".

μΰηψεπδ, ριιξδ θας δΰψλδ ωμ 36 ωαεςεϊ μωμα δψΰωεο ωμ πιρει ωμα llb, ωΰψκ 36 ωαεςεϊ εδψΰδ λι Laquinimod αξιπεο ωμ 0.6 βψν δωιβ ΰϊ διςγ δθιτεμι δψΰωεπι ωδεβγψ μπιρει. δπϊεπιν ωδϊχαμε αξδμκ ωμα δΰψλϊ δπιρει ξΰωψιν εξηζχιν ΰϊ δϊεφΰεϊ ωδϊχαμε α-36 δωαεςεϊ δψΰωεπιν ωμ πιρει ζδ. ξψαιϊ δηεμιν ωδωϊϊτε απιρει ξξωιλιν διεν μχαμ θιτεμ α-Laquinimod ξηχψ ΰχψΰι τϊεη.

"ϊηιμϊ ωμα 3 αξηχψ δχμιπι, ξρξμ ΰαο γψκ χψιθιϊ ςαεψ θας εξγβιω ΰϊ δξηειαεϊ ωμπε μχδιμϊ ηεμι δθψωϊ δπτεφδ", ΰεξψ ξωδ ξπεψ, ρξπλ"μ ξωΰαιν ιιηεγιιν αθας ϊςωιεϊ τψξφαθιεϊ ας"ξ. "ΰπηπε πψβωιν μχψΰϊ δξωκ δτιϊεη ωμ δ-Laquinimod, ΰωψ αιηγ ςν δχετχρεο ιψηια ΰϊ τμθτεψξϊ δϊλωιψιν ωμπε μθιτεμ αθψωϊ δπτεφδ ωμπε, ειξφα ΰϊ θας ληαψδ ξεαιμδ αϊηεν δθψωϊ δπτεφδ".

αχεπβψρ δ-23 ωμ ECTRIMS (δεεςιγδ δΰιψετιϊ μθιτεμ εξηχψ αθψωϊ πτεφδ) ωπςψκ α- 13 μΰεχθεαψ ατψΰβ, δεφβε ϊεφΰεϊ πιρει α- Laquinimod αξεγμ θψωϊ πτεφδ ααςμι ηιιν (ΰπφτμεξιμιθιρ ΰεθεΰιξεπιϊ, EAE) δξψΰεϊ λι δϊλωιψ δτηιϊ ΰϊ δγμχϊ, δτηιϊ ΰϊ ψξϊ δτβιςδ αξιΰμιο (γξιΰμιπφιδ) εΰϊ δπζχ μΰχρεο - γαψ δξψξζ λι μϊλωιψ ϊλεπεϊ ΰπθι- γμχϊιεϊ ειλεμεϊ δβπδ ςφαιϊ.

αδϊαρρ ςμ δϊεφΰεϊ δξςεγγεϊ ξδπιρει ααςμι ηιιν, πηχψ λιεν δωιξεω α-Laquinimod αξημεϊ ΰεθεΰιξεπιεϊ περτεϊ.

"ΰπηπε ξΰγ ωαςι ψφεο ξδφμηϊδ ωμ θας μχγν ΰϊ ϊλπιϊ δτιϊεη δχμιπι α-Laquinimod, αξθψδ μδαιΰ μωεχ ξεφψ ηγω, ξδγψβδ δβαεδδ αιεϊψ, μθιτεμ αθψωϊ πτεφδ", ΰεξψ ρεεο ΰπγψρεο, πωιΰ εξπλ"μ Active Biotech AB. διςιμεϊ, δαθιηεϊ εδραιμεϊ ωμ Laquinimod ιιηχψε αξρβψϊ πιρει περσ αωμα 3 (BRAVO), ωιιςψκ αχψα ηεμι RRMS, ΰωψ δψιωεν με φτει μδϊηιμ αψαςεο δψΰωεο ωμ 2008. ζδε ξηχψ βμεαΰμι, ψα-ξψλζι, εΰχψΰι, ΰωψ ιωεεδ ΰϊ δωτςϊ δθιτεμ α-Laquinimod μδωτςϊ ξϊο τμριαε οαπερσ ιρτχ δπιρει πϊεπι ριλεο-ϊεςμϊ αδωεεΰδ αιο Laquinimod αξϊο ΰεψΰμι τςν αιεν μαιο ξεφψ χιιν δξωξω διεν μθιτεμ α-RRMS (δωεεΰδ ΰχθιαιϊ). ξηχψ ζδ ξϊλπο μβιιρ λ-1,200 ξωϊϊτιν ωιθετμε μΰεψκ 24 ηεγωιν.

ΰεγεϊ ΰμβψε
ΰμβψε δεΰ ξηχψ βμεαΰμι, ψα-ξψλζι, ΰχψΰι, λτεμ ρξιεϊ, ααχψϊ τμριαε, δξϊηιμ λςϊ αβιεν ξθετμιν εξιεςγ μλμεμ λ-1,000 ηεμι RRMS. αξηχψ ιωϊϊτε ξψλζιν αΰψδ"α, χπγδ, ΰιψετδ ειωψΰμ. μτψθιν περτιν ΰεγεϊ ΰμβψε, αχψε αΰϊψ: www.tevaclinicaltrials.com.

ΰεγεϊ Liquinimod
Laquinimod διπδ ϊλωιψ ηγω, ΰιξεπεξεγεμθεψ, μωιξεω ιεξι αξϊο γψκ δτδ, ΰωψ τεϊη μθιτεμ αξημϊ δθψωϊ δπτεφδ. ηαψϊ Active Biotech τιϊηδ ΰϊ Laquinimod εψωξδ ΰεϊδ ϊηϊ ωξδ ωμ ηαψϊ θας ϊςωιεϊ τψξφαθιεϊ ας"ξ, αηεγω ιεπι 2004. πιρει ωμα llb, ωπςψκ α-306 ηεμιν, δεφβ αωπϊ 2007 αλπρ δωπϊι ωμ δΰχγξιδ δΰξψιχπιϊ μπειψεμεβιδ (AAN). δπϊεπιν δψΰε λι ωιξεω ΰεψΰμι ιεξι α-Laquinimid αξιπεο ωμ 0.6 ξ"β, δτηιϊ αΰετο ξωξςεϊι ΰϊ τςιμεϊ δξημδ λτι ωδεγβξδ ααγιχεϊ MRI - ιψιγδ ωμ 40% αδωεεΰδ μτμριαε (p=0.0048) αχψα ηεμι RRMS - ελι πψωξδ ραιμεϊ ψαδ μϊψετδ.

ξο δπϊεπιν ωδϊχαμε ςεμδ λι, ξιπεο ωμ 0.6 ξ"β ξτηιϊ ΰϊ τςιμεϊ δξημδ (μτι MRI) α-55% αδωεεΰδ μτμριαε. Laquinimod δψΰδ ΰτχθ ηζχ εψφισ αςμ ξωξςεϊ ρθθιρθιϊ ατψξθψιν περτιν ωμ MRI. απερσ, δψΰδ δξηχψ πθιιδ μδτηϊδ αωιςεψ δδϊχτιν δωπϊι αχψα δηεμιν εβιγεμ αξρτψ δηεμιν ωμΰ ηεε δϊχτιν λμμ, αδωεεΰδ μξϊο τμριαε. θιτεμιν α-0.3 εα-0.6 ξ"β διε ραιμιν ςν ξςθ ωιπειιν εςμιεϊ ϊμειεϊ-ξιπεο αΰπζιξι δλαγ. ςγ διεν, πιϊο δ-Laquinimod μ-460 ηεμιν, αξρβψϊ ξηχψιν χμιπιιν ωεπιν.

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 μϊςωιδ 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.

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® and Lotrel®, 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. In this press release, we present certain as adjusted numbers, which are non-GAAP financial measures. These numbers exclude items such as the effects of step-up of inventory upon acquisition, acquisition of R&D in process, product rights impairment, restructuring expenses, settlements and related tax effect. A reconciliation between the as adjusted numbers and the comparable GAAP measures is included later in this release. We provide such non-GAAP data because we believe that such supplemental data provide useful information to investors to better understand underlying trends in our business. However, adjusted financial measures are not, and should not be, viewed as a substitute for GAAP results. Our definition of these adjusted financial measures may differ from similarly named measures used by others.