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Michael Hayden - Articles and news items

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Teva completes acquisition of Labrys

Industry news / 21 July 2014 / Teva

…opens door to a strong and novel migraine prevention and treatment franchise within its CNS portfolio.

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Teva reports positive results from pivotal Phase III study to evaluate hydrocodone bitartrate extended-release tablets (CEP-33237) for moderate to severe chronic low back pain

Industry news / 30 April 2014 / Teva

Data provides promise for a twice-daily, acetaminophen-free hydrocodone designed with potential abuse-deterrent properties…

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Teva and OncoGenex announce top-line survival results of Phase III SYNERGY trial evaluating custirsen in combination with first-line docetaxel and prednisone for metastatic castrate-resistant prostate cancer

Industry news / 28 April 2014 / Teva

Teva Pharmaceutical Industries Ltd. and OncoGenex Pharmaceuticals, Inc. announced results from the Phase III SYNERGY trial…

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New data presented at 29th ECTRIMS Congress reinforce the clinical profile of investigational laquinimod on disease progression and inflammation in relapsing-remitting multiple sclerosis

Industry news / 4 October 2013 / Teva Pharmaceutical Industries Ltd

Pooled data analysis of Phase III ALLEGRO and BRAVO studies add to our understanding of investigational laquinimod for relapsing-remitting Multiple Sclerosis…

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Teva to present further results of twenty-year open-label extension study of glatiramer acetate 20 mg daily for relapsing-remitting Multiple Sclerosis

Industry news / 3 October 2013 / Teva Pharmaceutical Industries Ltd

“To our knowledge, glatiramer acetate is the only treatment for multiple sclerosis that has been prospectively studied for nearly two decades…”

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Newly published phase III exploratory analysis suggests investigational oral laquinimod for multiple sclerosis may reduce brain damage caused by neurodegeneration

Industry news / 1 October 2013 / Teva Pharmaceutical Industries Ltd

“This Phase III sub-study was pre-planned to explore the ability of laquinimod to act on mechanisms leading to irreversible brain tissue damage…”

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Teva reports top-line results from final Phase III study of armodafinil (NUVIGIL®) in patients with major depression associated with bipolar I disorder

Industry news, News / 30 August 2013 / Teva Pharmaceutical Industries Ltd

TEVA announced top-line results of its final Phase III clinical study for armodafinil (NUVIGIL®)…

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Teva receives European Marketing Authorization for Lonquex® (XM22 lipegfilgrastim)

Industry news, News / 8 August 2013 / Teva Pharmaceutical Industries Ltd

TEVA announced that the European Commission has granted marketing authorization for Lonquex® (lipegfilgrastim)…

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Teva’s Lonquex® (XM22 lipegfilgrastim) recommended for approval in the EU

Industry news, News / 3 June 2013 / Teva Pharmaceutical Industries Ltd

Teva’s Lonquex® (XM22 lipegfilgrastim) recommended for approval in the EU for the reduction of CIN…

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Teva announces FDA acceptance of sNDA for a higher concentration dose of COPAXONE® given three times a week

Industry news, News / 30 May 2013 / Teva Pharmaceutical Industries Ltd.

“We are pleased that the FDA has accepted for review our sNDA…”

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Teva and Xenon announce FDA orphan drug designation for pain drug XEN402

Industry news, News / 23 April 2013 / TEVA

“We are very pleased to receive orphan drug designation for XEN402…”

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Teva Pharmaceutical’s new investigational treatment for MS

Industry news, News / 21 March 2013 / PARADIGM COMMUNICATIONS

TEVA and Active Biotech announced top-line results from the open-label extension of the Phase III ALLEGRO study…

 

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