WithdrawnPhase 2NCT05085574
Leidos-Enabled Adaptive Protocol for Clinical Trials (LEAP-CT) in Hospitalized Patients With COVID-19 (Addendum 1)
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
- Leidos Life Sciences
- Principal Investigator
- Tilly Lawrence, BSN, RNLeidos, Inc.
- Intervention
- Famotidine(drug)
- Eligibility
- 18 years · All sexes
- Timeline
- 2023 – 2023
Collaborators
United States Department of Defense
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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