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NCT02039401 · ClinicalTrials.gov registry record · Phase 1

Safety Study of VM202 to Treat Amyotrophic Lateral Sclerosis

A Phase 1 study, sponsored by Helixmith Co..

Completed
Registry status
Phase 1
Development phase
18
Enrollment target

NCT02039401: Completed Phase 1 study, sponsored by Helixmith Co..

NCT02039401 is a Phase 1 study that has completed, run by Helixmith Co.. The registered enrollment target is 18 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (70% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02039401, a Phase 1 study, has completed, sponsored by Helixmith Co..

COMPLETED
Registry status
Phase 1
Development phase
18 participants
Enrollment target

Study Summary

The purpose of this study is to determine the safety and tolerability of intramuscular injections of VM202 at different injection sites in people with amyotrophic lateral sclerosis.

Primary Outcome

Adverse events (including serious adverse events, and adverse events leading to treatment discontinuation) throughout the 9 months follow-up. Descriptive statistics will be used to characterize safety parameters.

Interventions

  • BIOLOGICAL VM202

Trial Details

FieldValue
Enrollment Target 18 participants
Start Date 2014-03-11
Est. Completion 2024-03-06
Phase Phase 1
Helixmith Co.

12 total trials

What the finished NCT02039401 record still lists

NCT02039401 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 18 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (70% lower).

The record links to 0 conditions, and to 1 intervention - of which VM202 is the first listed.

NCT02039401 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02039401 about?

NCT02039401 is a clinical study titled "Safety Study of VM202 to Treat Amyotrophic Lateral Sclerosis". The purpose of this study is to determine the safety and tolerability of intramuscular injections of VM202 at different injection sites in people with amyotrophic lateral sclerosis.

What is the current status of trial NCT02039401?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 18 participants. The study started on 2014-03-11. Estimated completion is 2024-03-06.

What interventions are being tested in trial NCT02039401?

The interventions under investigation include: VM202 (BIOLOGICAL).

Who is sponsoring clinical trial NCT02039401?

This trial is sponsored by Helixmith Co., which has 12 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02039401's enrollment target sits among peer trials

18 1720th of 2000 higher than 216 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 NCT02039401, the US trial registry maintained by the National Library of Medicine. NCT02039401 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.