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COMPLETED Phase 2

Eight-Weeks Of Treatment With Talnetant In Subjects With Irritable Bowel Syndrome (IBS)

NCT00101985 · View on ClinicalTrials.gov ↗

Study Summary

This study will evaluate the effectiveness and safety of the investigational drug talnetant in treating subjects with irritable bowel syndrome (IBS).

Conditions Studied

Interventions

  • DRUG talnetant

Study Locations (20)

California

  • GSK Investigational Site — Carmichael
  • GSK Investigational Site — Concord
  • GSK Investigational Site — Garden Grove
  • GSK Investigational Site — Orange
  • GSK Investigational Site — Roseville
  • GSK Investigational Site — Spring Valley
  • GSK Investigational Site — Torrance

Colorado

  • GSK Investigational Site — Boulder
  • GSK Investigational Site — Centennial
  • GSK Investigational Site — Wheat Ridge

Connecticut

  • GSK Investigational Site — Bristol
  • GSK Investigational Site — Stamford
  • GSK Investigational Site — Torrington

Florida

  • GSK Investigational Site — DeLand
  • GSK Investigational Site — Miami
  • GSK Investigational Site — St. Petersburg

Arizona

  • GSK Investigational Site — Chandler
  • GSK Investigational Site — Phoenix

Arkansas

  • GSK Investigational Site — North Little Rock

Delaware

  • GSK Investigational Site — Newark

Trial Details

FieldValue
Enrollment Target 741 participants
Start Date 2004-10
Est. Completion 2005-07
Phase Phase 2

Sponsor

GlaxoSmithKline

558 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00101985

The ClinicalTrials.gov registry entry for NCT00101985 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 741 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is GlaxoSmithKline, which has 558 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Irritable Colon appearing as the primary indexed condition, and to 1 intervention — of which talnetant is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00101985 reports 20 study locations spanning 7 distinct geographic areas — top geographies include California, Colorado, Connecticut. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00101985 about?

NCT00101985 is a clinical study titled "Eight-Weeks Of Treatment With Talnetant In Subjects With Irritable Bowel Syndrome (IBS)". This study will evaluate the effectiveness and safety of the investigational drug talnetant in treating subjects with irritable bowel syndrome (IBS).

What is the current status of trial NCT00101985?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 741 participants. The study started on 2004-10. Estimated completion is 2005-07.

What conditions does trial NCT00101985 study?

This clinical trial studies the following conditions: Irritable Colon. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00101985?

The interventions under investigation include: talnetant (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00101985?

This trial is sponsored by GlaxoSmithKline, which has 558 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00101985 being conducted?

This trial has 20 study locations across Arizona, Arkansas, California, Colorado, Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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