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NCT01060254 · ClinicalTrials.gov registry record · Phase 2

A Study to Evaluate the Pain Relieving Effects, Safety, and Tolerability of JNJ-42160443 for the Relief of Bladder Pain

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

Terminated
Registry status
Phase 2
Development phase
31
Enrollment target

NCT01060254: Clinical Trial Phase 2 study, sponsored by Johnson & Johnson Pharmaceutical Research & Development, L.L.C..

NCT01060254 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 31 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (77% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01060254, 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
31 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the analgesic efficacy, safety, and tolerability of JNJ-42160443 compared to placebo in patients with moderate to severe, chronic bladder pain from interstitial cystitis and/or painful bladder syndrome.

Interventions

  • DRUG Placebo
  • DRUG JNJ-42160443

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2010-04-06
Est. Completion 2011-06-24
Phase Phase 2

Why NCT01060254 stopped before completion

NCT01060254 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 31 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (77% lower).

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

NCT01060254 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01060254 about?

NCT01060254 is a clinical study titled "A Study to Evaluate the Pain Relieving Effects, Safety, and Tolerability of JNJ-42160443 for the Relief of Bladder Pain". The purpose of this study is to evaluate the analgesic efficacy, safety, and tolerability of JNJ-42160443 compared to placebo in patients with moderate to severe, chronic bladder pain from interstitial cystitis and/or painful bladder syndrome.

What is the current status of trial NCT01060254?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 31 participants. The study started on 2010-04-06. Estimated completion is 2011-06-24.

What interventions are being tested in trial NCT01060254?

The interventions under investigation include: Placebo (DRUG), JNJ-42160443 (DRUG).

Who is sponsoring clinical trial NCT01060254?

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 NCT01060254's enrollment target sits among peer trials

31 1578th of 2000 higher than 419 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 NCT01060254, the US trial registry maintained by the National Library of Medicine. NCT01060254 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.