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AbbVie to Present Data on VIEKIRAX® (ombitasvir/paritaprevir/ritonavir...

(Source: AbbVie Inc) Mar 30, 2016 NORTH CHICAGO, Ill., March 30, 2016 /PRNewswire / -- AbbVie (NYSE: ABBV), a global biopharmaceutical company, today announced that 25 abstracts have been accepted for...

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AbbVie Announces New Phase 3b Results in Genotype 1b Chronic Hepatitis C...

NORTH CHICAGO, Ill., June 24, 2015 /PRNewswire/ -- AbbVie (NYSE: ABBV), a global biopharmaceutical company, today announced TURQUOISE-III study results demonstrating 100 percent (n=60/60) sustained...

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AbbVie Announces Real-World Data with VIEKIRAX®...

BARCELONA, Spain, April 15, 2016 /PRNewswire/ -- AbbVie (NYSE: ABBV), a global biopharmaceutical company, today announced new real-world data showing 96 percent of genotype 1 (GT1) patients (n=486/505...

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Enanta Pharmaceuticals Announces Data on Eight-Week Treatment of AbbVie’s...

(Source: Enanta Pharmaceuticals Inc) AbbVie reports 98 percent of previously untreatedgenotype 1b (GT1b) chronic hepatitis C virus (HCV) infected patients without cirrhosis achieved SVRin Phase 3b...

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Enanta Pharmaceuticals Announces Preliminary Data from AbbVie’s Phase 3b...

(Source: Enanta Pharmaceuticals Inc) Enanta Pharmaceuticals Announces Preliminary Data from AbbVie's Phase 3b RUBY-I Study in Chronic Hepatitis C Patients with Renal Impairment Presented at The...

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AbbVie Announces New Phase 3b Results in Genotype 1b Chronic Hepatitis C...

- 100 percent SVR(12) rate achieved with VIEKIRAX® (ombitasvir/paritaprevir/ritonavir tablets) + EXVIERA® (dasabuvir tablets) without ribavirin(1) NORTH CHICAGO, Ill., June 24, 2015 /PRNewswire/ --...

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AbbVie Announces New Phase 3b Results in Genotype 1b Chronic Hepatitis C...

(Source: AbbVie Inc) - 100 percent SVR(12) rate achieved with VIEKIRAX® (ombitasvir/paritaprevir/ritonavir tablets) + EXVIERA® (dasabuvir tablets) without ribavirin(1) NORTH CHICAGO, Ill. , June 24,...

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AbbVie to Present New Data from Hepatitis C Clinical Development Program at...

NORTH CHICAGO, Ill., April 8, 2015 /PRNewswire/ -- AbbVie (NYSE: ABBV) today announced that 29 abstracts from its ongoing hepatitis C clinical development program have been accepted for presentation...

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AbbVie to Present New Data from Hepatitis C Clinical Development Program at...

- 29 abstracts, including sub-analyses of AbbVie's approved treatment of VIEKIRAX® + EXVIERA®, as well as new data from Phase 3b development program and AbbVie's HCV pipeline compounds NORTH CHICAGO,...

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AbbVie to Present New Data from Hepatitis C Clinical Development Program at...

(Source: AbbVie Inc) - 29 abstracts, including sub-analyses of AbbVie's approved treatment of VIEKIRAX® + EXVIERA®, as well as new data from Phase 3b development program and AbbVie's HCV pipeline...

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Enanta Announces High SVR Rates with AbbVie’s VIEKIRAX® + EXVIERA® Regardless...

(Source: Enanta Pharmaceuticals Inc) 100 percent of genotype 1b (GT1b) patients who received VIEKIRAX + EXVIERA without ribavirin for 12 weeks, achieved SVRin a post-hoc analysis,regardless of whether...

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AbbVie Presents Late-Breaking, Preliminary Phase 3b Data with VIEKIRAX® +...

VIENNA, April 25, 2015 /PRNewswire/ -- AbbVie (NYSE: ABBV) today announced new, preliminary safety and efficacy data from the first cohort of its ongoing, Phase 3b RUBY-I study. RUBY-I is evaluating...

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AbbVie Presents Late-Breaking, Preliminary Phase 3b Data with VIEKIRAX® +...

- RUBY-I evaluates treatment-naïve, non-cirrhotic, genotype 1 chronic hepatitis C patients with severe renal impairment - In preliminary data from RUBY-I, patients receiving VIEKIRAX + EXVIERA with or...

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AbbVie Presents Late-Breaking, Preliminary Phase 3b Data with VIEKIRAX® +...

(Source: AbbVie Inc) - RUBY-I evaluates treatment-naïve, non-cirrhotic, genotype 1 chronic hepatitis C patients with severe renal impairment - In preliminary data from RUBY-I, patients receiving...

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AbbVie Announces High SVR Rates with VIEKIRAX®...

BARCELONA, Spain, April 14, 2016 /PRNewswire/ -- AbbVie (NYSE: ABBV), a global biopharmaceutical company, today announced data showing that patients with genotype 1 (GT1) chronic hepatitis C virus...

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ViiV Healthcare announces phase II study results for first two drug,...

(Source: GSK - GlaxoSmithKline plc) 32 week maintenance data presented at CROI showed comparable viral suppression rates between injectable regimen and three drug oral regimen Issued: London London,...

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First Regimen Combining Long Acting Injectable Antiretrovirals; 32-Week LATTE...

(Source: Johnson & Johnson) Intramuscular 2-drug maintenance therapy demonstrates comparable antiviral activity to daily oral 3-drug combination CORK, Ireland, - February 24, 2016 - Janssen...

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ViiV Healthcare begins phase III programme with dolutegravir/rilpivirine...

(Source: GSK - GlaxoSmithKline plc) 06 May 2015 First programme to evaluate dual HIV maintenance therapy with dolutegravir and rilpivirine London, United Kingdom, 6 May 2015: ViiV Healthcare today...

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ViiV Healthcare Begins Phase III Programme with dolutegravir/rilpivirine...

First programme to evaluate dual HIV maintenance therapy with dolutegravir and rilpivirine LONDON, May 6, 2015 /CNW/ - ViiV Healthcare today announced the start of a Phase III clinical trial programme...

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Janssen to Progress Collaboration with ViiV Healthcare to Develop the First...

(Source: Johnson & Johnson) 5bdf0770-87c8-4b68-992a-859cfe2ae0b0.pdf January 7, 2016 Janssen to Progress Collaboration with ViiV Healthcare to Develop the First Long Acting Two Drug Injectable...

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