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Expanded Access Treatment Protocol: Remdesivir (RDV; GS-5734) for the Treatment of SARS-CoV2 (CoV) Infection (COVID-19)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. Identifier: NCT04323761
Expanded Access Status : Available
First Posted : March 27, 2020
Last Update Posted : July 23, 2020
Information provided by (Responsible Party):
Gilead Sciences

Tracking Information
First Submitted Date March 24, 2020
First Posted Date March 27, 2020
Last Update Posted Date July 23, 2020
Descriptive Information
Brief Title Expanded Access Treatment Protocol: Remdesivir (RDV; GS-5734) for the Treatment of SARS-CoV2 (CoV) Infection (COVID-19)
Brief Summary The primary objective of this study is to provide expanded access of remdesivir (RDV) for the treatment of severe acute respiratory syndrome coronavirus (SARS-CoV2) infection.
Detailed Description Not Provided
Study Type Expanded Access
Expanded Access Type Treatment IND/Protocol
Intervention Drug: Remdesivir
Intravenous infusion administered over a 30 to 120 minute period
Other Names:
  • GS-5734™
  • Veklury®
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by Identifier (NCT Number) in Medline.
Recruitment Information
Expanded Access Status Available
Contact: Gilead Clinical Study Information Center 1-833-445-3230 (GILEAD-0)
Listed Location Countries Australia,   Austria,   Belgium,   Canada,   Cyprus,   Czechia,   Denmark,   Estonia,   France,   Germany,   Greece,   Hungary,   Iceland,   Ireland,   Israel,   Italy,   Netherlands,   Poland,   Portugal,   Romania,   Slovakia,   Slovenia,   Spain,   Switzerland,   United Kingdom,   United States
Removed Location Countries  
Administrative Information
NCT Number NCT04323761
Responsible Party Gilead Sciences
Study Sponsor Gilead Sciences
Collaborators Not Provided
Study Director: Gilead Study Director Gilead Sciences
PRS Account Gilead Sciences
Verification Date July 2020