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NCT00973024 · ClinicalTrials.gov registry record · Phase 2

A Dose-ranging Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Low Back Pain

A Phase 2 study, sponsored by Johnson & Johnson Pharmaceutical Research & Development, L.L.C..

Terminated
Registry status
Phase 2
Development phase
389
Enrollment target

NCT00973024: Clinical Trial Phase 2 study, sponsored by Johnson & Johnson Pharmaceutical Research & Development, L.L.C..

NCT00973024 is a Phase 2 study that was terminated before completion, run by Johnson & Johnson Pharmaceutical Research & Development, L.L.C.. The registered enrollment target is 389 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (192% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00973024, a Phase 2 study, was terminated before completion, sponsored by Johnson & Johnson Pharmaceutical Research & Development, L.L.C..

TERMINATED
Registry status
Phase 2
Development phase
389 participants
Enrollment target

Study Summary

The purpose of this study is to compare the safety and effectiveness of different doses of JNJ-42160443 with placebo in the treatment of chronic, moderate to severe low back pain patients with a diagnosis of chronic low back pain.

Interventions

  • DRUG Matching Placebo
  • DRUG JNJ-42160443 3 mg
  • DRUG JNJ-42160443 1 mg
  • DRUG JNJ-42160443 6 mg/3mg
  • DRUG JNJ-42160443 10 mg

Trial Details

FieldValue
Enrollment Target 389 participants
Start Date 2009-09
Est. Completion 2011-05
Phase Phase 2

Why NCT00973024 stopped before completion

NCT00973024 is an interventional study that assigns participants to a tested intervention. The registered 389 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (192% higher).

The record links to 0 conditions, and to 5 interventions - of which Matching Placebo is the first listed.

NCT00973024 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00973024 about?

NCT00973024 is a clinical study titled "A Dose-ranging Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Low Back Pain". The purpose of this study is to compare the safety and effectiveness of different doses of JNJ-42160443 with placebo in the treatment of chronic, moderate to severe low back pain patients with a diagnosis of chronic low back pain.

What is the current status of trial NCT00973024?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 389 participants. The study started on 2009-09. Estimated completion is 2011-05.

What interventions are being tested in trial NCT00973024?

The interventions under investigation include: Matching Placebo (DRUG), JNJ-42160443 3 mg (DRUG), JNJ-42160443 1 mg (DRUG), JNJ-42160443 6 mg/3mg (DRUG), JNJ-42160443 10 mg (DRUG).

Who is sponsoring clinical trial NCT00973024?

This trial is sponsored by Johnson & Johnson Pharmaceutical Research & Development, L.L.C., which has 102 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00973024's enrollment target sits among peer trials

389 108th of 2000 higher than 1,892 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 NCT00973024, the US trial registry maintained by the National Library of Medicine. NCT00973024 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.