Biopharmaceutical company Gilead Sciences Inc (Nasdaq:GILD) announced on Friday that it is donating more than 2,000 vials of remdesivir to the Republic of Uganda to support response efforts to the Ebola Bundibugyo virus disease (BVD) outbreak.
The intravenous antiviral therapy is being provided under compassionate use and Monitored Emergency Use of Unregistered and Investigational Interventions (MEURI) frameworks.
Gilead is also preparing additional support for requests from the Democratic Republic of the Congo, the World Health Organization, and other partners, including remdesivir and the investigational oral antiviral obeldesivir, alongside planned clinical trials. The initiative reflects Gilead's decade-long engagement in outbreak response across Sub-Saharan Africa through emergency, compassionate, and investigational use donations, the company said.
Remdesivir has shown preclinical activity against multiple filoviruses but is not approved for filovirus disease in any country, and its safety and efficacy for the Bundibugyo strain have not been established. It is approved for COVID-19 treatment in approximately 50 countries and has been administered to more than 14.5 million patients globally, including over 8.1 million in low- and middle-income countries.
Gilead noted that remdesivir's clinical efficacy for Ebola Bundibugyo virus disease remains unproven and is being evaluated through ongoing studies.
Sensei Biotherapeutics changes name to Faeth Therapeutics
Bayer receives FDA approval for AMBELVIST MRI contrast agent
AstraZeneca secures US approval for Truqap combination in PTEN‑deficient prostate cancer
Menarini reports Phase 3 data for selinexor plus ruxolitinib in myelofibrosis
Gilead Sciences mobilises remdesivir donation to support Ebola response in Uganda
Airiver Medical treats first chronic rhinosinusitis patient in Drug Coated Balloon clinical study
Precigen and the RRPF recognise International RRP Awareness Day
Roche secures IVDR approval to expand VENTANA MMR RxDx Panel indications
Guardant Health expands FDA-approved companion diagnostic use for HERNEXEOS
FDA grants priority review for Genentech's Tecentriq in stage III dMMR/MSI-H colon cancer
Harbour BioMed IND for HBM7004 accepted by China's NMPA
Organon secures FDA approval expanding TOFIDENCE indications for CRS and paediatric COVID-19