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AbbVie Announces New Data on VIEKIRA PAK® (ombitasvir, paritaprevir,...

NORTH CHICAGO, Ill., Nov. 14, 2015 /PRNewswire/ -- AbbVie (NYSE: ABBV), a global biopharmaceutical company, today announced new data from its ongoing Phase 3b TOPAZ-II study evaluating VIEKIRA PAK®...

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AbbVie Announces New Data on VIEKIRA PAK® (ombitasvir, paritaprevir,...

(Source: AbbVie Inc) NORTH CHICAGO, Ill., Nov. 14, 2015/PRNewswire / -- AbbVie (NYSE: ABBV), a global biopharmaceutical company, today announced new data from its ongoing Phase 3b TOPAZ-II study...

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AbbVie Announces FDA Acceptance of New Drug Application for a Once-Daily...

NORTH CHICAGO, Ill., Dec. 2, 2015 /PRNewswire/ -- AbbVie (NYSE: ABBV), a global biopharmaceutical company, today announced its New Drug Application (NDA) has been accepted by the U.S. Food and Drug...

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AbbVie Announces FDA Acceptance of New Drug Application for a Once-Daily...

(Source: AbbVie Inc) NORTH CHICAGO, Ill., Dec. 2, 2015/PRNewswire / -- AbbVie (NYSE: ABBV), a global biopharmaceutical company, today announced its New Drug Application (NDA) has been accepted by the...

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Enanta Pharmaceuticals Announces U.S. Regulatory Approval of TECHNIVIE™...

(Source: Enanta Pharmaceuticals Inc) Enanta Pharmaceuticals Announces U.S. Regulatory Approval of TECHNIVIE™ (ombitasvir, paritaprevir and ritonavir) tablets The First and Only All-Oral Interferon-Free...

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AbbVie Demonstrates Commitment to Hepatitis C Patients with New Data on...

NORTH CHICAGO, Ill., Oct. 1, 2015 /PRNewswire/ -- AbbVie (NYSE: ABBV), a global research-based biopharmaceutical company, today announced that 34 abstracts from its chronic hepatitis C clinical...

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AbbVie Demonstrates Commitment to Hepatitis C Patients with New Data on...

NORTH CHICAGO, Ill., Oct. 1, 2015 /PRNewswire/ -- AbbVie (NYSE: ABBV), a global research-based biopharmaceutical company, today announced that 34 abstracts from its chronic hepatitis C clinical...

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AbbVie Demonstrates Commitment to Hepatitis C Patients with New Data on...

(Source: AbbVie Inc) NORTH CHICAGO, Ill., Oct. 1, 2015/PRNewswire / -- AbbVie (NYSE: ABBV), a global research-based biopharmaceutical company, today announced that 34 abstracts from its chronic...

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Enanta Pharmaceuticals Announces FDA Acceptance of AbbVie’s New Drug...

(Source: Enanta Pharmaceuticals Inc) Decision from FDA on New Drug Application anticipated in second half of 2016 Regimen contains Enanta’s lead protease inhibitor, paritaprevir WATERTOWN,...

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Enanta Announces New Data on VIEKIRA PAK® (ombitasvir, paritaprevir,...

(Source: Enanta Pharmaceuticals Inc) AbbVie’s ongoing TOPAZ-II study evaluates long-term treatment outcomes in genotype 1a and genotype 1b chronic HCV patients with or without compensated cirrhosis...

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U.S. FDA Grants Priority Review to AbbVie for Supplemental New Drug...

NORTH CHICAGO, Ill., Jan. 7, 2016 /PRNewswire/ -- AbbVie (NYSE: ABBV), a global biopharmaceutical company, today announced that the U.S. Food and Drug Administration (FDA) has accepted its supplemental...

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Enanta Pharmaceuticals Announces the U.S. FDA Grants Priority Review to...

(Source: Enanta Pharmaceuticals Inc) Priority review designation shortens the regulatory review period from the standard 10 months to six months TURQUOISE-III study showed 100 percent sustained...

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FDA Grants Priority Review to AbbVie for Supplemental New Drug Application...

(Source: AbbVie Inc) NORTH CHICAGO, Ill., Jan. 7, 2016/PRNewswire / -- AbbVie (NYSE: ABBV), a global biopharmaceutical company, today announced that the U.S. Food and Drug Administration (FDA) has...

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AbbVie Receives CHMP Positive Opinion for VIEKIRAX®...

NORTH CHICAGO, Ill., Feb. 26, 2016 /PRNewswire/ -- AbbVie (NYSE: ABBV), a global biopharmaceutical company, announced today that the European Committee for Medicinal Products for Human Use (CHMP) of...

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AbbVie Receives CHMP Positive Opinion for VIEKIRAX®...

NORTH CHICAGO, Ill., Feb. 26, 2016 /PRNewswire/ -- AbbVie (NYSE: ABBV), a global biopharmaceutical company, announced today that the European Committee for Medicinal Products for Human Use (CHMP) of...

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Enanta Announces the U.S. Food and Drug Administration has approved AbbVie’s...

(Source: Enanta Pharmaceuticals Inc) New once-daily, extended-release co-formulation contains the three direct-acting antiviral components of VIEKIRA PAK® for adult patients with genotype 1 (GT1)...

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Enanta Announces U.S. FDA has Approved AbbVie’s Supplemental New Drug...

(Source: Enanta Pharmaceuticals Inc) Approval supported by TURQUOISE-III study showing 100 percent SVR (N=60/60) in chronic hepatitis C virus (HCV) infected genotype 1b patients with compensated...

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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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TECHNIVIE(TM) (ombitasvir, paritaprevir, and ritonavir tablets) Receives FDA...

- TECHNIVIE provides an opportunity to treat adults in the U.S. who have genotype 4 (GT4) chronic hepatitis C virus (HCV) infection without cirrhosis, a population historically considered...

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AbbVie's VIEKIRAX® (ombitasvir/paritaprevir/ritonavir tablets) Receives...

NORTH CHICAGO, Ill., Sept. 28, 2015 /PRNewswire/ -- AbbVie (NYSE: ABBV), a global biopharmaceutical company, today announced that the Japanese Ministry of Health, Labour and Welfare (MHLW) approved...

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AbbVie's VIEKIRAX® (ombitasvir/paritaprevir/ritonavir tablets) Receives...

(Source: AbbVie Inc) NORTH CHICAGO, Ill., Sept. 28, 2015/PRNewswire / -- AbbVie (NYSE: ABBV), a global biopharmaceutical company, today announced that the Japanese Ministry of Health, Labour and...

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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 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 Announces CHMP Grants Positive Opinion for an Eight-Week Treatment...

CHMP opinion is a step closer to the approval of an eight-week regimen of VIEKIRAX + EXVIERA for previously untreated genotype 1b (GT1b) chronic hepatitis C virus (HCV) patients with minimal to...

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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 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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TECHNIVIE™ (ombitasvir, paritaprevir, and ritonavir tablets) Receives FDA...

(Source: AbbVie Inc) - TECHNIVIE provides an opportunity to treat adults in the U.S. who have genotype 4 (GT4) chronic hepatitis C virus (HCV) infection without cirrhosis, a population historically...

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TECHNIVIE™ (ombitasvir, paritaprevir, and ritonavir tablets) Receives FDA...

NORTH CHICAGO, Ill., July 24, 2015 /PRNewswire/ -- AbbVie (NYSE: ABBV), a global, research-based biopharmaceutical company, today announced that the U.S. Food and Drug Administration (FDA) approved...

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Lupin Bolsters US Brands Portfolio with Methergine® Oral Tablets

MUMBAI, India and BALTIMORE, April 28, 2016 /PRNewswire/ -- The only FDA-approved oral uterotonic for the management of PPH, comes to market with a significant investment in professional medical...

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Merck Applauds the U.S. Department of Veterans Affairs (VA) for Broadening...

(Source: Merck & Co Inc) KENILWORTH, N.J.--(BUSINESS WIRE)--Merck (NYSE:MRK), known as MSD outside the United States and Canada, applauds the U.S. Department of Veterans Affairs (VA) for broadening...

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Merck to Present New Findings from Chronic Hepatitis C Clinical Development...

(Source: Merck & Co Inc) KENILWORTH, N.J.--(BUSINESS WIRE)--Merck (NYSE:MRK), known as MSD outside of the United States and Canada, today announced the planned presentations of data from the...

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Merck Announces Results From Phase 3 Studies of ZEPATIER(TM) (Elbasvir and...

Merck (NYSE:MRK), known as MSD outside of the United States and Canada, today announced the presentation of results from two Phase 3 clinical trials evaluating ZEPATIER™ (elbasvir and grazoprevir)...

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Merck Announces Results From Phase 3 Studies of ZEPATIER™ (Elbasvir and...

(Source: Merck & Co Inc) KENILWORTH, N.J.--(BUSINESS WIRE)--Merck (NYSE:MRK), known as MSD outside of the United States and Canada, today announced the presentation of results from two Phase 3...

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AbbVie Receives CHMP Positive Opinion for Eight-Week Treatment Option with...

- CHMP opinion brings AbbVie one step closer to approval of an eight-week regimen of VIEKIRAX + EXVIERA for previously untreated genotype 1b (GT1b) chronic hepatitis C virus (HCV) patients with minimal...

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Merck’s ZEPATIER™ (Elbasvir and Grazoprevir) Showed Superiority on Efficacy...

(Source: Merck & Co Inc) KENILWORTH, N.J.--(BUSINESS WIRE)--Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today announced the presentation of results from C-EDGE...

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Merck Receives FDA Approval of ZEPATIER™ (elbasvir and grazoprevir) for the...

(Source: Merck & Co Inc) KENILWORTH, N.J.--(BUSINESS WIRE)--Merck (NYSE:MRK), known as MSD outside the United States and Canada, today announced that the U.S. Food and Drug Administration (FDA) has...

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Bristol-Myers Squibb Receives U.S. FDA Breakthrough Therapy Designation for...

(Source: Bristol-Myers Squibb Company) BMS-663068 is the first investigational antiretroviral designed to prevent HIV attachment to and entry into CD4+ T cells FDA Breakthrough Designation recognizes...

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Janssen Submits Supplemental New Drug Application to U.S. FDA for All-Oral,...

(Source: Johnson & Johnson) July 23, 2015 Janssen Submits Supplemental New Drug Application to U.S. FDA for All-Oral, Once-Daily OLYSIO® (Simeprevir) in Combination with Sofosbuvir Filing Supported...

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Janssen Submits Supplemental New Drug Application to U.S. FDA for All-Oral,...

TITUSVILLE, N.J., July 23, 2015 /PRNewswire/ -- Janssen Therapeutics, Division of Janssen Products, LP (Janssen), today announced the submission of a supplemental New Drug Application (sNDA) to the...

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Your Story, Your HIV Wisdom™ Brings Together HIV Voices and Supports HIV...

(Source: Johnson & Johnson) Notable HIV Advocates Highlight Perspectives of People Living with or Affected by HIV to Leverage Shared Support and Self-Expression TITUSVILLE, N.J., September 8, 2015...

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Your Story, Your HIV Wisdom™ Brings Together HIV Voices and Supports HIV...

TITUSVILLE, N.J., Sept. 8, 2015 /PRNewswire/ -- Seeking and sharing information are important parts of the HIV journey – in fact, 80 percent of people living with HIV said they give advice or tell...

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U.S. FDA Approves PREZISTA® (darunavir) for Use in Pregnant Women with HIV...

(Source: Johnson & Johnson) Data shows PREZISTA is a safe and effective treatment option in pregnant women, with no reports of mother-to-child HIV transmission among women who continued therapy...

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