Urtė Fultinavičiūtė

Urtė Fultinavičiūtė

Reporter

London, UK

Urtė has previously worked as a Healthcare Reporter at GlobalData Media, primarily writing for Clinical Trials Arena. She mostly focused on clinical trial data management, strategy, and regulatory updates as well as clinical trial data readouts and exclusive interviews with C-level pharma and biotech executives. Urtė holds an MA in International Journalism from City, University of London.

Latest from Urtė Fultinavičiūtė

TEST: Samsung Bioepis Hit With Denosumab Lawsuit

Amgen has asserted 34 patents for alleged infringement against Samsung Bioepis, which is the highest number out of the three lawsuits filed by the originator against a denosumab biosimilar maker.

TEST: Generics And Biosimilars Saved $445bn In 2023

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Regulatory Recap: FTC And Others Support Biosimilar Interchangeability Draft Guidance

Generics Bulletin reviews the latest regulatory events across the world.

Off-Patent Industry Criticizes CMS’ Negotiated Price Drug List

Off-patent industry groups in the US have raised questions about why Stelara is included on the list and if CMS’ projection can match up with estimated savings that could be generated traditionally by generics and biosimilars.

Lucentis And Stelara Biosimilars Drive Formycon’s 2024 Financials

Despite reporting lower revenues in the first half of the year, Formycon continues to see value in its biosimilar projects, with a new candidate to be launched in the second half of 2024.

Samsung Bioepis Hit By Amgen Denosumab Lawsuit

Amgen has asserted 34 patents for alleged infringement against Samsung Bioepis, which is the highest number out of the three lawsuits filed by the originator against a denosumab biosimilar maker.