
The World Health Organization’s Chief Scientist Soumya Swaminathan has warned that experts and regulators assessing the use of Gilead’s remdesivir …

The FDA has approved Gilead’s antiviral therapy Veklury (remdesivir) for the treatment of hospitalised COVID-19 patients, making it the first …

Gilead has revealed promising new Phase 3 data reinforcing the non-inferiority of Biktarvy (bictegravir 50mg/emtricitabine 200mg/tenofovir alafenamide 25mg) compared to …

As Europe continues to face down a rising second wave of COVID-19, the European Commission quickly moved to secure a …

The European Commission (EC) has signed a new joint procurement agreement (JPA) with pharma firm Gilead to improve access to …

Gilead and Eisai have secured approval for their oral JAK1 preferential inhibitor Jyseleca (filgotinib) from the Japanese Ministry of Health, …

Gilead has agreed to pay $97 million to resolve claims from the US Government that it used an independent charity …

The Board of Directors from both companies have unanimously agreed for Gilead to acquire Immunomedics for $88 per share in …

Gilead and Jounce Therapeutics have come together in a new immuno-oncology partnership potentially worth over $700 million. The primary drive …

The FDA could expand its Emergency Use Authorization (EUA) for Gilead’s remdesivir for treating coronavirus patients, according to Gilead.

Gilead’s JAK inhibitor filgotinib has been unexpectedly knocked back by the FDA as a therapy to treat moderately to severely …

New research has warned that minority groups and people of colour are underrepresented in current trials for COVID-19 therapies, despite …

Gilead Sciences has asked the FDA to approve its drug remdesivir to treat COVID-19 patients. The drug would go under …

Kite Pharma has chalked up another regulatory success for its parent company Gilead with the news that the FDA has …

Mylan has launched its own generic version of Gilead’s remdesivir on the Indian market for the treatment of patients with …