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COMPLETED Phase 2

A Multicenter Assessment of LBR-101 in High Frequency Episodic Migraine

NCT02025556 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to determine whether monthly subcutaneous administration of LBR-101 (fremanezumab) is safe and provides migraine prevention in subjects with high frequency episodic migraine.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG LBR-101 High Dose
  • DRUG LBR-101 Low Dose

Study Locations (20)

California

  • Teva Investigational Site 161 — Anaheim
  • Teva Investigational Site 116 — Fullerton
  • Teva Investigational Site 119 — Long Beach
  • Teva Investigational Site 146 — Oceanside
  • Teva Investigational Site 113 — San Francisco
  • Teva Investigational Site 108 — Stanford
  • Teva Investigational Site 112 — Walnut Creek

Florida

  • Teva Investigational Site 143 — DeLand
  • Teva Investigational Site 137 — Hialeah
  • Teva Investigational Site 159 — Hollywood
  • Teva Investigational Site 101 — Jacksonville
  • Teva Investigational Site 166 — Jacksonville
  • Teva Investigational Site 129 — Maitland
  • Teva Investigational Site 167 — Orlando

Arizona

  • Teva Investigational Site 145 — Gilbert
  • Teva Investigational Site 130 — Phoenix
  • Teva Investigational Site 117 — Scottsdale

Arkansas

  • Teva Investigational Site 158 — Little Rock

Colorado

  • Teva Investigational Site 132 — Boulder

Connecticut

  • Teva Investigational Site 162 — Stamford

Trial Details

FieldValue
Enrollment Target 297 participants
Start Date 2014-01-31
Est. Completion 2015-03-31
Phase Phase 2

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02025556

The ClinicalTrials.gov registry entry for NCT02025556 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 297 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Teva Branded Pharmaceutical Products R&D, which has 103 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 Episodic Migraine Headache appearing as the primary indexed condition, and to 3 interventions — of which Placebo 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: NCT02025556 reports 20 study locations spanning 6 distinct geographic areas — top geographies include California, Florida, Arizona. 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 NCT02025556 about?

NCT02025556 is a clinical study titled "A Multicenter Assessment of LBR-101 in High Frequency Episodic Migraine". The purpose of this study is to determine whether monthly subcutaneous administration of LBR-101 (fremanezumab) is safe and provides migraine prevention in subjects with high frequency episodic migraine.

What is the current status of trial NCT02025556?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 297 participants. The study started on 2014-01-31. Estimated completion is 2015-03-31.

What conditions does trial NCT02025556 study?

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

What interventions are being tested in trial NCT02025556?

The interventions under investigation include: Placebo (DRUG), LBR-101 High Dose (DRUG), LBR-101 Low Dose (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02025556?

This trial is sponsored by Teva Branded Pharmaceutical Products R&D, which has 103 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02025556 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