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who is behind gilead sciences

Through the COMPASS (COMmitment to Partnership in Addressing HIV/AIDS in Southern States) program, Gilead has pledged $100 million over 10 years to support efforts to reduce HIV-related stigma and inequalities that disproportionately impact people living in the South. Here's what could happen next. Who bought or sold Gilead Sciences this quarter? The U.S. Food and Drug Administration approves Letairis® for the treatment of pulmonary arterial hypertension. Gilead Sciences, Inc. is a biotechnology company specializing in developing and marketing drugs to treat antiviral diseases. 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, as a pharmaceutical developer, would require substantial amounts of capital to finance its research, capital that could not be recouped for years, perhaps even decades. However, the biotech stock opened for trading at a little over $22 per share -- a gain of nearly 47% right off the bat for early investors. Remdesivir is $1000-under 50% effective. Between 1998 and 2001, the company's sales increased 501 percent, pushed upward by the growing popularity of Gilead's portfolio of pharmaceuticals. © 2020 Gilead Sciences, Inc. All rights reserved. Some people had never even heard of Gilead before its COVID-19 program garnered widespread publicity. In May 2001, the company applied for FDA market approval of Tenofovir DF, an oral tablet that blocked reverse transcriptase, an enzyme crucial to the replication of HIV. The company expects to soon announce results from late-stage testing of remdesivir in treating COVID-19. Truvada is added to Gilead's Access Program and U.S. Aside from its work related to HIV and AIDS, Gilead also markets a drug to treat the flu, a pharmaceutical marketed by the company as Tamiflu, and a drug to treat fungal infections, which is marketed under the name AmBisome. The company has researched the drug since 2009, originally as a potential treatment for hepatitis C and respiratory syncytial virus and then later for the Ebola virus and now COVID-19. The program later became part of the U.S. His long wait nearly over, Riordan hoped to obtain FDA approval within six months, setting the stage for Vistide's debut in the U.S. market for late 1996. Sweetening the pot for Gilead was NeXstar's European and Australian sales force, which would prove useful as the company exerted itself as an international drug developer and marketer. Gilead-developed HIV medicines reach more than 10 million people in the developing world. The program facilitates access to Vistide, a medicine for the eye infection cytomegalovirus retinitis that was once common among people living with HIV. The U.S. Food and Drug Administration approves Vemlidy®, a once-daily treatment for adults with chronic hepatitis B virus (HBV) infection with compensated liver disease. Gilead's IPO would not be the last time Riordan turned to Wall Street for cash. The U.S. Food and Drug Administration approves Epclusa®, the first all-oral, pan-genotypic, single tablet regimen for the treatment of adults with genotype 1-6 chronic hepatitis C virus (HCV) infection.

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