WithdrawnPhase 1NCT01593072
A Study to Assess the Safety, Tolerability and Pharmacokinetics of AVI-7537 in Healthy Adult Volunteers
Studying Ebola hemorrhagic fever
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
- Sarepta Therapeutics, Inc.
- Principal Investigator
- Alison Heald, MDSarepta Therapeutics, Inc.
- Intervention
- AVI-7537(drug)
- Eligibility
- 18-50 years · All sexes
- Timeline
- 2012 – 2013
Study locations (1)
- Quintiles Phase I Services, Overland Park, Kansas, United States
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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