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NCT01566877 · ClinicalTrials.gov registry record · Phase 1

A Study to Assess the Safety, Tolerability and Pharmacokinetics of AVI-7288 in Healthy Adult Volunteers

A Phase 1 study of Marburg Hemorrhagic Fever, sponsored by Sarepta Therapeutics.

Completed
Registry status
Phase 1
Development phase
40
Enrollment target
1
Study location

NCT01566877: Completed Phase 1 study of Marburg Hemorrhagic Fever, sponsored by Sarepta Therapeutics.

NCT01566877 is a Phase 1 study of Marburg Hemorrhagic Fever that has completed, run by Sarepta Therapeutics. The registered enrollment target is 40 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (33% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01566877, a Phase 1 study of Marburg Hemorrhagic Fever, has completed, sponsored by Sarepta Therapeutics.

COMPLETED
Registry status
Phase 1
Development phase
40 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to evaluate the safety and tolerability of healthy male and female subjects with intravenous (IV) infusions of AVI 7288 compared to matched placebo in and to evaluate the pharmacokinetics (PK).

Conditions Studied

Interventions

  • OTHER Placebo
  • DRUG AVI-7288

Study Locations (1)

Maryland

  • SNBL Clinical Pharmacology Center, Inc. - Baltimore

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2013-05
Est. Completion 2014-01
Phase Phase 1
Sarepta Therapeutics

33 total trials

What the finished NCT01566877 record still lists

NCT01566877 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (33% lower).

The record links to 1 condition, with Marburg Hemorrhagic Fever appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT01566877 reports a single indexed study location in Maryland.

Frequently Asked Questions

What is clinical trial NCT01566877 about?

NCT01566877 is a clinical study titled "A Study to Assess the Safety, Tolerability and Pharmacokinetics of AVI-7288 in Healthy Adult Volunteers". The purpose of this study is to evaluate the safety and tolerability of healthy male and female subjects with intravenous (IV) infusions of AVI 7288 compared to matched placebo in and to evaluate the pharmacokinetics (PK).

What is the current status of trial NCT01566877?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 40 participants. The study started on 2013-05. Estimated completion is 2014-01.

What conditions does trial NCT01566877 study?

This clinical trial studies the following conditions: Marburg Hemorrhagic Fever.

What interventions are being tested in trial NCT01566877?

The interventions under investigation include: Placebo (OTHER), AVI-7288 (DRUG).

Who is sponsoring clinical trial NCT01566877?

This trial is sponsored by Sarepta Therapeutics, which has 33 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01566877 being conducted?

This trial has 1 study location across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

How this trial's enrollment target compares

Where NCT01566877's enrollment target sits among peer trials

40 1130th of 2000 higher than 810 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01566877, the US trial registry maintained by the National Library of Medicine. NCT01566877 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.