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NCT02018250 · ClinicalTrials.gov registry record · Phase 1

Study to Evaluate the Safety of a New Oxime, MMB4 DIMETHANESULFONATE (DMS)

A Phase 1 study, sponsored by U.S. Army Medical Research and Development Command.

Completed
Registry status
Phase 1
Development phase
32
Enrollment target

NCT02018250: Completed Phase 1 study, sponsored by U.S. Army Medical Research and Development Command.

NCT02018250 is a Phase 1 study that has completed, run by U.S. Army Medical Research and Development Command. The registered enrollment target is 32 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (47% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02018250, a Phase 1 study, has completed, sponsored by U.S. Army Medical Research and Development Command.

COMPLETED
Registry status
Phase 1
Development phase
32 participants
Enrollment target

Study Summary

This clinical study will evaluate escalating dosages of MMB4 DMS to determine its safety when delivered intramuscularly (i.m.) to the anterior thigh.

Interventions

  • DRUG Placebo
  • DRUG MMB4 DMS

Trial Details

FieldValue
Enrollment Target 32 participants
Start Date 2012-03-17
Est. Completion 2012-12
Phase Phase 1

What the finished NCT02018250 record still lists

NCT02018250 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 32 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (47% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT02018250 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02018250 about?

NCT02018250 is a clinical study titled "Study to Evaluate the Safety of a New Oxime, MMB4 DIMETHANESULFONATE (DMS)". This clinical study will evaluate escalating dosages of MMB4 DMS to determine its safety when delivered intramuscularly (i.m.) to the anterior thigh.

What is the current status of trial NCT02018250?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 32 participants. The study started on 2012-03-17. Estimated completion is 2012-12.

What interventions are being tested in trial NCT02018250?

The interventions under investigation include: Placebo (DRUG), MMB4 DMS (DRUG).

Who is sponsoring clinical trial NCT02018250?

This trial is sponsored by U.S. Army Medical Research and Development Command, which has 77 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02018250's enrollment target sits among peer trials

32 1296th of 2000 higher than 679 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 NCT02018250, the US trial registry maintained by the National Library of Medicine. NCT02018250 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.