Safety Study of Single Administration Post-Exposure Prophylaxis Treatment for Ebola Virus

Completed · Phase 1 · Has a placebo group

Conditions studied: Ebola Hemorrhagic Fever

In brief

The purpose of this study is to characterize the safety and pharmacology of single administrations of AVI-6002, a post-exposure prophylaxis candidate treatment for Ebolavirus.

Key facts

Study ID

NCT01353027

Run by

Sarepta Therapeutics, Inc.

People needed

30

Starts

2010-05-01

Expected to finish

2011-11-01

Last updated by the study team

2012-03-28

Who can join

Age: 18 and older, up to 50. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Male or female and between the ages of 18 and 50 years in good general health
• Volunteers must be willing to use barrier methods of contraception or be of non-childbearing potential
• Volunteers must be willing to undergo a urine screen for drugs of abuse

You may not qualify if…

• Pregnancy or breastfeeding.
• Any clinically relevant abnormalities in physical examinations, vital signs, ECG, clinical chemistry, hematology or urinalysis
• Positive test for human immunodeficiency virus, hepatitis B or hepatitis C or known history of HIV infection

Where it is running

• New Orleans Center for Clinical Research - Knoxville — Knoxville, Tennessee, United States

Full record on ClinicalTrials.gov

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