Expanded Access Treatment Protocol: Remdesivir (RDV; GS-5734) for the Treatment of SARS-CoV2 (CoV) Infection (COVID-19)
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ClinicalTrials.gov Identifier: NCT04323761 |
Expanded Access Status :
Approved for marketing
First Posted : March 27, 2020
Last Update Posted : November 13, 2020
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Sponsor:
Gilead Sciences
Information provided by (Responsible Party):
Gilead Sciences
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Tracking Information | ||||
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First Submitted Date | March 24, 2020 | |||
First Posted Date | March 27, 2020 | |||
Last Update Posted Date | November 13, 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:
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Publications * | Not Provided | |||
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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Recruitment Information | ||||
Expanded Access Status | Approved for marketing | |||
Contacts | Contact information is only displayed when the study is recruiting subjects | |||
Listed Location Countries | Australia, Austria, Belgium, Canada, Cyprus, Czechia, Denmark, Estonia, France, Germany, Greece, Hungary, Iceland, Ireland, Israel, Italy, Lithuania, Netherlands, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Switzerland, United Kingdom, United States | |||
Removed Location Countries | ||||
Administrative Information | ||||
NCT Number | NCT04323761 | |||
Current Responsible Party | Gilead Sciences | |||
Original Responsible Party | Same as current | |||
Current Study Sponsor | Gilead Sciences | |||
Original Study Sponsor | Same as current | |||
Collaborators | Not Provided | |||
Investigators |
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PRS Account | Gilead Sciences | |||
Verification Date | November 2020 |