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NCT01259050 · ClinicalTrials.gov registry record · Phase 1

Safety Study of High Doses of Zinc in ALS Patients

A Phase 1 study, sponsored by Phoenix Neurological Associates.

Completed
Registry status
Phase 1
Development phase
10
Enrollment target

NCT01259050: Completed Phase 1 study, sponsored by Phoenix Neurological Associates.

NCT01259050 is a Phase 1 study that has completed, run by Phoenix Neurological Associates. The registered enrollment target is 10 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (83% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01259050, a Phase 1 study, has completed, sponsored by Phoenix Neurological Associates.

COMPLETED
Registry status
Phase 1
Development phase
10 participants
Enrollment target

Study Summary

The purpose of this study is to determine the safety of Zinc given at 90mg/d in conjunction with 2mg/d of copper in ALS patients.

Interventions

  • DRUG Zinc and Copper

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2010-10
Est. Completion 2012-03
Phase Phase 1
Phoenix Neurological Associates

4 total trials

What the finished NCT01259050 record still lists

NCT01259050 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (83% lower).

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

NCT01259050 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01259050 about?

NCT01259050 is a clinical study titled "Safety Study of High Doses of Zinc in ALS Patients". The purpose of this study is to determine the safety of Zinc given at 90mg/d in conjunction with 2mg/d of copper in ALS patients.

What is the current status of trial NCT01259050?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 10 participants. The study started on 2010-10. Estimated completion is 2012-03.

What interventions are being tested in trial NCT01259050?

The interventions under investigation include: Zinc and Copper (DRUG).

Who is sponsoring clinical trial NCT01259050?

This trial is sponsored by Phoenix Neurological Associates, which has 4 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01259050's enrollment target sits among peer trials

10 1913th of 2000 higher than 46 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 NCT01259050, the US trial registry maintained by the National Library of Medicine. NCT01259050 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.