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NCT02239172 · ClinicalTrials.gov registry record · Phase 1

PA83-FhCMB Plant-Derived Recombinant Protective Antigen (rPA) Anthrax Vaccine

A Phase 1 study of Anthrax, sponsored by Fraunhofer, Center for Molecular Biotechnology.

Completed
Registry status
Phase 1
Development phase
30
Enrollment target
1
Study location

NCT02239172: Completed Phase 1 study of Anthrax, sponsored by Fraunhofer, Center for Molecular Biotechnology.

NCT02239172 is a Phase 1 study of Anthrax that has completed, run by Fraunhofer, Center for Molecular Biotechnology. The registered enrollment target is 30 participants, below the 773-participant average among 6 other Anthrax trials with a reported enrollment target (96% 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

NCT02239172, a Phase 1 study of Anthrax, has completed, sponsored by Fraunhofer, Center for Molecular Biotechnology.

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

Study Summary

The purposes of this study is to evaluate and compare the safety, reactogenicity, and tolerability of the PA83-FhCMB vaccine candidate delivered at 4 dose levels with Alhydrogel

Conditions Studied

Interventions

  • BIOLOGICAL PA83-FhCMB

Study Locations (1)

Maryland

  • Walter Reed Army Institute of Research, Clinical Trials Center - Silver Spring

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2014-08
Est. Completion 2015-05
Phase Phase 1

What the finished NCT02239172 record still lists

NCT02239172 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 773-participant average among 6 other Anthrax trials with a reported enrollment target (96% lower).

The record links to 1 condition, with Anthrax appearing as the primary indexed condition, and to 1 intervention - of which PA83-FhCMB is the first listed.

NCT02239172 reports a single indexed study location in Maryland.

Frequently Asked Questions

What is clinical trial NCT02239172 about?

NCT02239172 is a clinical study titled "PA83-FhCMB Plant-Derived Recombinant Protective Antigen (rPA) Anthrax Vaccine". The purposes of this study is to evaluate and compare the safety, reactogenicity, and tolerability of the PA83-FhCMB vaccine candidate delivered at 4 dose levels with Alhydrogel

What is the current status of trial NCT02239172?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 2014-08. Estimated completion is 2015-05.

What conditions does trial NCT02239172 study?

This clinical trial studies the following conditions: Anthrax.

What interventions are being tested in trial NCT02239172?

The interventions under investigation include: PA83-FhCMB (BIOLOGICAL).

Who is sponsoring clinical trial NCT02239172?

This trial is sponsored by Fraunhofer, Center for Molecular Biotechnology, which has 4 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02239172 being conducted?

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

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Source: ClinicalTrials.gov NCT02239172, the US trial registry maintained by the National Library of Medicine. NCT02239172 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.