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NCT04160091 · ClinicalTrials.gov registry record · Phase 2

Study to Evaluate the Efficacy and Safety of FX006 in Patients With Glenohumeral Osteoarthritis or Shoulder Adhesive Capsulitis

A Phase 2 study, sponsored by Pacira Pharmaceuticals.

Terminated
Registry status
Phase 2
Development phase
19
Enrollment target

NCT04160091: Clinical Trial Phase 2 study, sponsored by Pacira Pharmaceuticals.

NCT04160091 is a Phase 2 study that was terminated before completion, run by Pacira Pharmaceuticals. The registered enrollment target is 19 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (86% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04160091, a Phase 2 study, was terminated before completion, sponsored by Pacira Pharmaceuticals.

TERMINATED
Registry status
Phase 2
Development phase
19 participants
Enrollment target

Study Summary

This is a double-blind study to evaluate the efficacy and safety of FX006 in patients with glenohumeral osteoarthritis (OA) or shoulder adhesive capsulitis (AC).

Primary Outcome

The pain intensity score is measured using an 11-point numeric rating scale (NRS), where 0 indicates "No pain" and 10 indicates "Worst possible pain."

Interventions

  • DRUG Normal Saline
  • DRUG FX006

Trial Details

FieldValue
Enrollment Target 19 participants
Start Date 2019-11-07
Est. Completion 2020-06-15
Phase Phase 2
Pacira Pharmaceuticals

88 total trials

Why NCT04160091 stopped before completion

NCT04160091 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 19 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (86% lower).

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

NCT04160091 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04160091 about?

NCT04160091 is a clinical study titled "Study to Evaluate the Efficacy and Safety of FX006 in Patients With Glenohumeral Osteoarthritis or Shoulder Adhesive Capsulitis". This is a double-blind study to evaluate the efficacy and safety of FX006 in patients with glenohumeral osteoarthritis (OA) or shoulder adhesive capsulitis (AC).

What is the current status of trial NCT04160091?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 19 participants. The study started on 2019-11-07. Estimated completion is 2020-06-15.

What interventions are being tested in trial NCT04160091?

The interventions under investigation include: Normal Saline (DRUG), FX006 (DRUG).

Who is sponsoring clinical trial NCT04160091?

This trial is sponsored by Pacira Pharmaceuticals, which has 88 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04160091's enrollment target sits among peer trials

19 1894th of 2000 higher than 103 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT04160091, the US trial registry maintained by the National Library of Medicine. NCT04160091 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.