CompletedPhase 4NCT05911906
An Open-label, Clinical Feasibility Study of the Efficacy of Remdesivir for Long-COVID.
Studying Severe acute respiratory syndrome
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- University of Derby
- Principal Investigator
- Victoria Allgar, PhDPen CTU
- Intervention
- Remdesivir(drug)
- Enrollment
- 73 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2024 – 2025
Study locations (4)
- University of Derby, Derby, Derby, United Kingdom
- Derbyshire Community Health Services NHS Foundation Trust, Chesterfield, United Kingdom
- Royal Derby Hospital (UHDB), Derby, United Kingdom
- University of Exeter / Royal Devon University Healthcare NHS FT, Exeter, United Kingdom
Collaborators
University of Exeter · University of Plymouth · University Hospitals of Derby and Burton NHS Foundation Trust · Aston University · Royal Devon and Exeter NHS Foundation Trust
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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