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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 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.

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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

What the Registry Record Tells You About NCT01060254

The ClinicalTrials.gov registry entry for NCT01060254 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 31 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Johnson & Johnson Pharmaceutical Research & Development, L.L.C., which has 102 total studies on file at ClinicalTrials.gov.

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

NCT01060254 reports 0 study locations.

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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.