Company is seeking monetary damages from the alleged violation.
Believing the multinational company violated four patents relating to the use of Antigens in Arexvy, GSK has announced the filing of a lawsuit against Pfizer. According to the documents filed in court, Pfizer’s respiratory syncytial virus (RSV) vaccine, Abrysvo, was created with GSK’s “claimed inventions”. With GSK seeking monetary damages such as lost profits, Pfizer has denied any infringement, planning to defend its work.
As both Arexvy and Abrysvo have already received FDA approval, doses are now available to the public for use in adults over 60. As a part of legal proceedings, GSK has requested authorities to prevent Pfizer from selling its product.
Reference: GSK Sues Pfizer for Alleged RSV Vaccine Patent Infringement. BioSpace. August 2, 2023. Accessed August 3, 2023. https://www.biospace.com/article/gsk-sues-pfizer-for-alleged-rsv-vaccine-patent-infringement/?s=89
Addressing Disparities in Psoriasis Trials: Takeda's Strategies for Inclusivity in Clinical Research
April 14th 2025LaShell Robinson, Head of Global Feasibility and Trial Equity at Takeda, speaks about the company's strategies to engage patients in underrepresented populations in its phase III psoriasis trials.
Beyond the Prescription: Pharma's Role in Digital Health Conversations
April 1st 2025Join us for an insightful conversation with Jennifer Harakal, Head of Regulatory Affairs at Canopy Life Sciences, as we unpack the evolving intersection of social media and healthcare decisions. Discover how pharmaceutical companies can navigate regulatory challenges while meaningfully engaging with consumers in digital spaces. Jennifer shares expert strategies for responsible marketing, working with influencers, and creating educational content that bridges the gap between patients and healthcare providers. A must-listen for pharma marketers looking to build trust and compliance in today's social media landscape.
FDA Approves Nipocalimab for the Treatment of Generalized Myasthenia Gravis
April 30th 2025Approval is based on results from the pivotal Vivacity-MG3 trial in which IMAAVY (nipocalimab-aahu) demonstrated superior disease control throughout 24 weeks when compared to placebo plus standard of care.