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AbbVie and Eisai Subsidiary EA Pharma Commence Co-promotion of Fully Human Anti-TNF-a Monoclonal Antibody HUMIRAยฎ in the Field of Gastrointestinal Disease

AbbVie GK announced that EA Pharma and AbbVie will commence the co-promotion of fully human anti-TNF-ฮฑ monoclonal antibody HUMIRAยฎ for indications in the field of gastrointestinal disease. Established in April 2016 through the integration of Eisai's...

GlaxoSmithKline plans to file NDA in U.S. for FF/UMEC/VI in patients with COPD

GlaxoSmithKline plc and Innoviva, Inc announced that, following discussions with the US FDA ,GSK has brought forward the plan to file a NDA in the US for the once-daily closed triple combination therapy, fluticasone furoate/umeclidinium/vilanterol (FF/UMEC/VI; a combination inhaled...

AbbVies Research Commitment to Helping People Living with Rheumatologic Diseases Highlighted Annual EULAR 2016

AbbVie a global biopharmaceutical company announced that data on HUMIRAยฎ (adalimumab), investigational medicines and research, including real-world evidence, aiming to improve clinical outcomes for patients with rheumatologic diseases, will be presented at the Annual European Congress of Rheumatology (EULAR...

PAREXEL Named Company of the Year for the Pharmaceuticals Industry with a Gold Stevie from The American Business Awards

PAREXEL International Corporation ,a leading global biopharmaceutical services provider, has been named Company of the Year โ€“ Pharmaceuticals in the 14th Annual American Business AwardsSM. The judges awarded PAREXEL a Gold Stevieยฎ Award and recognized the...

Biogens Investigational Alzheimers Disease Treatment Aducanumab Accepted into European Medicines Agencys PRIME Program

Biogen announced that aducanumab, its investigational treatment for early Alzheimerโ€™s disease (AD), was accepted into the European Medicines Agencyโ€™s (EMA) Priority Medicines (PRIME) program. PRIME aims to bring treatments to patients faster by enhancing the EMAโ€™s support for the...

Otsuka Holdings Announces New, Additional Certification Under โ€œISO 22301โ€ (International Standard for Business Continuity Management)

Expands scope of certification to include additional Otsuka Group products, reflecting the companyโ€™s improved resiliency and continuous operational capability during unexpected events. Otsuka Holdings Co Ltd is pleased to announce that its subsidiary Taiho Pharmaceutical Co.,...

Amgen Receives Positive CHMP Opinion To Extend Indication Of Kyprolisยฎ (Carfilzomib) For The Treatment Of Relapsed Multiple Myeloma

Amgen announced that theCommittee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency has adopted a positive opinion to extend the current indication for Kyprolisยฎ (carfilzomib) to include treatment in combination with dexamethasone alone for adult...

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