GSK accelerates delivery timeline for US quadrivalent flu vaccine.
GlaxoSmithKline (GSK) announced July 16, 2015 that it has begun shipping its Fluarix Quadrivalent (influenza vaccine) doses to US healthcare providers, following licensing and lot-release approval from FDA's Center for Biologics Evaluation and Research. The company announced that it had shifted its supply to four-strain (quadrivalent) flu vaccine rather than trivalent vaccine.
"With flu a priority focus of our portfolio, we have made a significant investment in customer service upgrades, designed to accelerate delivery timelines to customers,” said said Patrick Desbiens, senior vice-president, US Vaccines, in a press release. GSK also has received 2015–2016 US license approval for its other quadrivalent flu vaccine, Flulaval Quadrivalent (influenza vaccine). Pending additional FDA lot releases, GSK expects to begin shipping Flulaval Quadrivalent in August 2015. Fluarix Quadrivalent comes in a 0.5-mL, single-dose, prefilled syringe while Flulaval Quadrivalent comes in a 5-mL, multidose vial containing 10 doses (0.5 mL each). Fluarix Quadrivalent is manufactured in Dresden, Germany. Flulaval Quadrivalent is manufactured in Ste-Foy, Quebec, Canada.
GSK expects to supply an estimated 32–38 million doses across both vaccines for the US market for the 2015–2016 season. The company shipped approximately 27 million doses for the 2014–2015 season (19 million quadrivalent and eight million trivalent). This year’s anticipated volume of quadrivalent doses is nearly double the amount shipped in 2014. GSK made the decision to switch to 100% quadrivalent following customer demand from the 2014–2015 flu season and early prebooking for the 2015–2016 season.
Source: GSK
Drug Solutions Podcast: A Closer Look at mRNA in Oncology and Vaccines
April 30th 2024In this episode fo the Drug Solutions Podcast, etherna’s vice-president of Technology and Innovation, Stefaan De Koker, discusses the merits and challenges of using mRNA as the foundation for therapeutics in oncology as well as for vaccines.
Drug Solutions Podcast: Applying Appropriate Analytics to Drug Development
March 26th 2024In this episode of the Drug Solutions Podcast, Jan Bekker, Vice President of Business Development, Commercial and Technical Operations at BioCina, discusses the latest analytical tools and their applications in the drug development market.
Entering New Domains for 3D Printing of Drug Products
April 6th 20253D printing of personalized medications is currently possible under existing compounding regulations, offering enhanced process control through automation. But new legislation coming in 2025 will allow 3D printing as part of a distributed manufacturing framework.