An open letter from our Chairman & CEO Daniel O’Day about our investigational antiviral for the treatment of COVID-19. Senators on Trial Diversity, Gilead Sciences Statement on NEJM Publication of Remdesivir Data From NIAID Study, Gilead Sciences Statement on Expanding Global Supply of Investigational Antiviral Remdesivir, Gilead Statement on Complaint Against Federal Government in The Court of Federal Claims, Gilead Sciences Statement on Data From Remdesivir Study in Patients With Severe COVID-19 in China, Gilead Sciences Response to Médecins Sans Frontières, Gilead Sciences Statement on Request to Rescind Remdesivir Orphan Drug Designation, Gilead Sciences Statement on Ensuring Continued Supply of HIV Medicine Amid Coronavirus Outbreak, Gilead Sciences Statement on Access to Remdesivir Outside of Clinical Trials, Gilead Statement on U.S. Patent and Trademark Office Decision to Deny Request for Inter Partes Review of HIV PrEP Patents, Gilead Sciences Statement on the Company’s Ongoing Response to the 2019 Novel Coronavirus (2019-nCoV), Gilead Statement on Commitment to Advancing Descovy for PrEP™ Study in Cisgender Women & Adolescent Females, Gilead Statement on U.S. Government Complaint Regarding HIV PrEP and PEP Patents, Petitions to US Patent and Trademark Office on HIV PrEP Patents, Gilead Sciences Statement on U.S. Preventive Services Task Force 'A' Recommendation for PrEP as an HIV Prevention Strategy, Gilead Sciences to Release Third Quarter 2020 Financial Results on Wednesday, October 28, 2020, Gilead Sciences Announces Expiration of Hart-Scott-Rodino Waiting Period for Immunomedics Tender Offer. ", First published on April 30, 2020 / 5:58 PM. Gilead is awaiting results of a trial of remdesivir, which previously failed as an Ebola treatment, in 400 patients hospitalized with severe COVID-19, with data expected later this month. "Although a 31% improvement [in a lengthy recovery time] doesn't seem like a knockout 100%, it is a very important proof of concept," Fauci said, noting that "what it is proving is that a drug can block this virus.". And that's raising a host of questions about the medication, ranging from its clinical benefits to its potential cost. Researchers at Boston’s Beth Israel Deaconess Medical Center have also heard that the two Gilead studies would stop enrolling patients by the end of the month. © 2020 Gilead Sciences, Inc. All rights reserved. Powered and implemented by FactSet. The FDA could decide to authorize emergency use of drug, Pitts said. Gilead Medical Resource Center. Still, experts say remdesivir is likely to play only one part in the broader public health response to the coronavirus, while its commercial importance to Gilead remains to be determined, even as enthusiastic investors drove up its stock price nearly 10% in recent days. Remdesivir is causing "rapid recoveries in fever and …

"The initial indication is that Gilead is doing the right thing from a public health perspective.". United, American and Delta drop change fees. "That's important because it's lives saved, but it doesn't save 50%," said Peter Pitts, president of the Center for Medicine in the Public Interest and a former associate commissioner with the U.S. Food and Drug Administration. "There are antibody cocktails that are being evaluated, and then obviously we have the vaccine trials that will start to generate data over next few months. “We would like to see equitable and transparent distribution of this very precious resource,” Dr. Helen Boucher, chief of infectious diseases at Tufts Medical Center in Boston, told Reuters. Together, we’re creating what’s possible. Remdesivir, sold under the brand name Veklury, is a broad-spectrum antiviral medication developed by the biopharmaceutical company Gilead Sciences. Interest in Gilead’s drug has been high given some promising early data and the lack of approved treatments or preventive vaccines for COVID-19, the disease caused by the novel coronavirus that has infected over 4 million people and killed more than 305,000 worldwide. "As part of the FDA's commitment to expediting the development and availability of potential COVID-19 treatments, the agency has been engaged in sustained and ongoing discussions with Gilead Sciences regarding making remdesivir available to patients as quickly as possible, as appropriate," the FDA spokesman said in a statement to CBS News. / MoneyWatch. Senators on Trial Diversity, Gilead Sciences Statement on NEJM Publication of Remdesivir Data From NIAID Study, Gilead Sciences Statement on Expanding Global Supply of Investigational Antiviral Remdesivir, Gilead Statement on Complaint Against Federal Government in The Court of Federal Claims, Gilead Sciences Statement on Data From Remdesivir Study in Patients With Severe COVID-19 in China, Gilead Sciences Response to Médecins Sans Frontières, Gilead Sciences Statement on Request to Rescind Remdesivir Orphan Drug Designation, Gilead Sciences Statement on Ensuring Continued Supply of HIV Medicine Amid Coronavirus Outbreak, Gilead Sciences Statement on Access to Remdesivir Outside of Clinical Trials, Gilead Statement on U.S. Patent and Trademark Office Decision to Deny Request for Inter Partes Review of HIV PrEP Patents, Gilead Sciences Statement on the Company’s Ongoing Response to the 2019 Novel Coronavirus (2019-nCoV), Gilead Statement on Commitment to Advancing Descovy for PrEP™ Study in Cisgender Women & Adolescent Females, Gilead Statement on U.S. Government Complaint Regarding HIV PrEP and PEP Patents, Petitions to US Patent and Trademark Office on HIV PrEP Patents, Gilead Sciences Statement on U.S. Preventive Services Task Force 'A' Recommendation for PrEP as an HIV Prevention Strategy, Download Full U.S. Prescribing Information, including BOXED WARNING, Download Full U.S. Prescribing Information.



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