UPDATE 2-U.S. FDA approves Gilead triple HIV drug, rival files lawsuit [Reuters]
GSK plc American Depositary Shares (Each representing two Ordinary Shares) (GSK)
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Source: Reuters
UPDATE 2-U.S. FDA approves Gilead triple HIV drug, rival files lawsuit | Reuters Reuters Staff 2 Min Read (Adds details on Glaxo lawsuit, updates share price) By Deena Beasley Feb 7 (Reuters) - The U.S. Food and Drug Administration on Wednesday approved Biktarvy, Gilead Sciences Inc’s once-daily triple-combination tablet for treatment of HIV infection, paving the way for the biotech company to capture more of the multibillion-dollar HIV drug market. Rival ViiV Healthcare, a joint venture majority-owned by GlaxoSmithKline Plc with Pfizer Inc and Shionogi Ltd, quickly filed a lawsuit alleging that Gilead is infringing patents on ViiV’s dolutegravir, a component of the venture’s triple-drug HIV treatment Triumeq. Officials at Gilead did not immediately respond to a request for comment on the lawsuit. Biktarvy combines new integrase inhibitor bictegravir with Descovy, an older medication that combines nucleoside reverse transcriptase inhibitors emtricitabine and tenofovir alafenamide. The
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- 4/19/24 - Form 6-K
- 4/17/24 - Form 6-K
- 4/17/24 - Form 6-K
- GSK's page on the SEC website