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Completed Phase 2 Interventional Results available

Assessment of LBR-101 In Chronic Migraine

ClinicalTrials.gov ID: NCT02021773

Public ClinicalTrials.gov record NCT02021773. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jun 26, 2026, 6:50 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Double-Blind, Double-Dummy, Placebo-Controlled, Parallel Group, Multi-dose Study Comparing the Efficacy and Safety of Subcutaneous LBR-101 With Placebo for the Preventive Treatment of Chronic Migraine

Study identification

NCT ID
NCT02021773
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Teva Branded Pharmaceutical Products R&D, Inc.
Industry
Enrollment
264 participants

Conditions and interventions

Interventions

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

Drug

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 30, 2014
Primary completion
Feb 27, 2015
Completion
Mar 30, 2015
Last update posted
Dec 8, 2021

2014 – 2015

United States locations

U.S. sites
57
U.S. states
22
U.S. cities
54
Facility City State ZIP Site status
Teva Investigational Site 145 Gilbert Arizona 85234
Teva Investigational Site 130 Phoenix Arizona 85032
Teva Investigational Site 117 Scottsdale Arizona 85259
Teva Investigational Site 161 Anaheim California 92801
Teva Investigational Site 116 Fullerton California 92835
Teva Investigational Site 119 Long Beach California 90806
Teva Investigational Site 146 Oceanside California 92056
Teva Investigational Site 113 San Francisco California 94109
Teva Investigational Site 108 Stanford California 94305
Teva Investigational Site 112 Walnut Creek California 94598
Teva Investigational Site 132 Boulder Colorado 80304
Teva Investigational Site 162 Stamford Connecticut 06905
Teva Investigational Site 143 DeLand Florida 32720
Teva Investigational Site 137 Hialeah Florida 33012
Teva Investigational Site 101 Jacksonville Florida 32216
Teva Investigational Site 166 Jacksonville Florida 32256
Teva Investigational Site 129 Maitland Florida 32751
Teva Investigational Site 167 Orlando Florida 32801
Teva Investigational Site 139 Ormond Beach Florida 32174
Teva Investigational Site 140 Port Orange Florida 32127
Teva Investigational Site 149 Atlanta Georgia 30342
Teva Investigational Site 164 Decatur Georgia 30030
Teva Investigational Site 134 Douglasville Georgia 30134
Teva Investigational Site 125 Evansville Indiana 47714
Teva Investigational Site 133 Lenexa Kansas 66214
Teva Investigational Site 135 Brockton Massachusetts 02301
Teva Investigational Site 124 New Bedford Massachusetts 02740
Teva Investigational Site 151 Springfield Massachusetts 01104
Teva Investigational Site 109 Watertown Massachusetts 02472
Teva Investigational Site 115 Worcester Massachusetts 01605
Teva Investigational Site 110 Ann Arbor Michigan 48104
Teva Investigational Site 114 Kalamazoo Michigan 49009
Teva Investigational Site 150 Golden Valley Minnesota 55422
Teva Investigational Site 152 Kansas City Missouri 64114
Teva Investigational Site 107 Springfield Missouri 65807
Teva Investigational Site 104 St Louis Missouri 63141
Teva Investigational Site 148 Reno Nevada 89502
Teva Investigational Site 105 The Bronx New York 10461
Teva Investigational Site 131 Greensboro North Carolina 27405-6962
Teva Investigational Site 118 Raleigh North Carolina 27607
Teva Investigational Site 168 Winston-Salem North Carolina 27103
Teva Investigational Site 122 Canton Ohio 44718
Teva Investigational Site 141 Cincinnati Ohio 45227
Teva Investigational Site 142 Cincinnati Ohio 45229-3039
Teva Investigational Site 155 Cleveland Ohio 44195
Teva Investigational Site 102 Columbus Ohio 43221
Teva Investigational Site 127 Oklahoma City Oklahoma 73112
Teva Investigational Site 111 Philadelphia Pennsylvania 19107
Teva Investigational Site 120 Goose Creek South Carolina 29445
Teva Investigational Site 153 Bristol Tennessee 37620
Teva Investigational Site 126 Memphis Tennessee 38119
Teva Investigational Site 154 Nashville Tennessee 37203
Teva Investigational Site 128 Arlington Texas 76012
Teva Investigational Site 121 Austin Texas 78731
Teva Investigational Site 136 Austin Texas 78745
Teva Investigational Site 123 Charlottesville Virginia 22911
Teva Investigational Site 144 Roanoke Virginia 24018

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02021773, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 8, 2021 · Synced Jun 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02021773 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →