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Completed Phase 3 Interventional Results available

Efficacy and Safety of Subcutaneous Administration of Fremanezumab (TEV-48125) for the Preventive Treatment of Migraine

ClinicalTrials.gov ID: NCT02638103

Public ClinicalTrials.gov record NCT02638103. 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 Oct 17, 2026, 2:29 PM 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, Parallel-Group Study Evaluating the Long-Term Safety, Tolerability, and Efficacy of Subcutaneous Administration of Fremanezumab (TEV-48125) for the Preventive Treatment of Migraine

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

A study to evaluate the long-term safety, tolerability, and efficacy of subcutaneous (SC) administration of TEV-48125 in adult participants with chronic migraine (CM) or episodic migraine (EM). Participants with CM or EM who complete the pivotal efficacy studies of TEV-48125 (TV48125-CNS-30049 \[NCT02621931\] and TV48125-CNS-30050 \[NCT02629861\]) and agree to participate in this study; and new participants meeting eligibility criteria (not rolling over from pivotal studies), will be enrolled in this study.

Study identification

NCT ID
NCT02638103
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
1,890 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 70 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
Feb 26, 2016 (Actual)
Primary completion
Jun 6, 2018 (Actual)
Completion
Dec 8, 2018 (Actual)
Last update posted
Nov 9, 2021

2016 – 2018

United States locations

U.S. sites
90
U.S. states
37
U.S. cities
78
Facility City State ZIP Site status
Teva Investigational Site 13628 Birmingham Alabama 35211 —
Teva Investigational Site 13577 Birmingham Alabama 35216 —
Teva Investigational Site 13606 Phoenix Arizona 85018 —
Teva Investigational Site 13579 Phoenix Arizona 85023 —
Teva Investigational Site 13602 Little Rock Arkansas 72205 —
Teva Investigational Site 13568 Encino California 91316 —
Teva Investigational Site 13546 Fullerton California 92835 —
Teva Investigational Site 13540 Long Beach California 90806 —
Teva Investigational Site 13632 Redlands California 92374 —
Teva Investigational Site 13571 Redondo Beach California 90277 —
Teva Investigational Site 13573 San Diego California 92103 —
Teva Investigational Site 13538 Santa Monica California 90404 —
Teva Investigational Site 13594 Santa Rosa California 95405 —
Teva Investigational Site 13595 Walnut Creek California 94598 —
Teva Investigational Site 13629 Aurora Colorado 80014 —
Teva Investigational Site 13557 Boulder Colorado 80301 —
Teva Investigational Site 13593 Colorado Springs Colorado 80918 —
Teva Investigational Site 13633 Denver Colorado 80210 —
Teva Investigational Site 13612 Denver Colorado 80239 —
Teva Investigational Site 13631 Englewood Colorado 80113 —
Teva Investigational Site 13563 East Hartford Connecticut 06118 —
Teva Investigational Site 13550 Stamford Connecticut 06905 —
Teva Investigational Site 13635 Bradenton Florida 34201 —
Teva Investigational Site 13597 Gainesville Florida 32607 —
Teva Investigational Site 13607 Hialeah Florida 33012 —
Teva Investigational Site 13559 Jacksonville Florida 32205 —
Teva Investigational Site 13584 Ocala Florida 34471 —
Teva Investigational Site 13587 Orlando Florida 32806 —
Teva Investigational Site 13567 Palm Beach Gardens Florida 33410 —
Teva Investigational Site 13553 Pembroke Pines Florida 33026 —
Teva Investigational Site 13616 Pinellas Park Florida 33781 —
Teva Investigational Site 13620 Atlanta Georgia 30312 —
Teva Investigational Site 13537 Atlanta Georgia 30342 —
Teva Investigational Site 13604 Boise Idaho 83642 —
Teva Investigational Site 13585 Chicago Illinois 60607 —
Teva Investigational Site 13621 Chicago Illinois 60654 —
Teva Investigational Site 13627 Evanston Illinois 60201 —
Teva Investigational Site 13596 Indianapolis Indiana 46254 —
Teva Investigational Site 13617 Wichita Kansas 67207 —
Teva Investigational Site 13598 Wichita Kansas 67211 —
Teva Investigational Site 13566 Louisville Kentucky 40207 —
Teva Investigational Site 13603 Metairie Louisiana 70006 —
Teva Investigational Site 13582 Pikesville Maryland 21208 —
Teva Investigational Site 13590 Boston Massachusetts 02131 —
Teva Investigational Site 13589 New Bedford Massachusetts 02301 —
Teva Investigational Site 13543 Watertown Massachusetts 02472 —
Teva Investigational Site 13539 Ann Arbor Michigan 48104 —
Teva Investigational Site 13542 Golden Valley Minnesota 55422 —
Teva Investigational Site 13534 Kansas City Missouri 64114 —
Teva Investigational Site 13536 Springfield Missouri 65807 —
Teva Investigational Site 13619 St Louis Missouri 63141 —
Teva Investigational Site 13618 Fremont Nebraska 68025 —
Teva Investigational Site 13605 Las Vegas Nevada 89106 —
Teva Investigational Site 13578 Lebanon New Hampshire 03756 —
Teva Investigational Site 13575 Martinsville New Jersey 08836 —
Teva Investigational Site 13622 Princeton New Jersey 08540 —
Teva Investigational Site 13588 Albuquerque New Mexico 87102 —
Teva Investigational Site 13576 Amherst New York 14226 —
Teva Investigational Site 13565 Plainview New York 11803 —
Teva Investigational Site 13544 Greensboro North Carolina 27405 —
Teva Investigational Site 13574 Greensboro North Carolina 27408 —
Teva Investigational Site 13545 Raleigh North Carolina 27612 —
Teva Investigational Site 13609 Akron Ohio 44311 —
Teva Investigational Site 13625 Akron Ohio 44311 —
Teva Investigational Site 13634 Akron Ohio 44311 —
Teva Investigational Site 13533 Cincinnati Ohio 45227 —
Teva Investigational Site 13624 Cincinnati Ohio 45249 —
Teva Investigational Site 13569 Cleveland Ohio 44195 —
Teva Investigational Site 13626 Columbus Ohio 43212 —
Teva Investigational Site 13561 Oklahoma City Oklahoma 73112 —
Teva Investigational Site 13601 Eugene Oregon 97401 —
Teva Investigational Site 13591 Jenkintown Pennsylvania 19046 —
Teva Investigational Site 13554 Philadelphia Pennsylvania 19107 —
Teva Investigational Site 13608 Uniontown Pennsylvania 15401 —
Teva Investigational Site 13615 Greer South Carolina 29650 —
Teva Investigational Site 13556 Mt. Pleasant South Carolina 29464 —
Teva Investigational Site 13560 Bristol Tennessee 37620 —
Teva Investigational Site 13551 Memphis Tennessee 38119 —
Teva Investigational Site 13532 Nashville Tennessee 37203 —
Teva Investigational Site 13552 Nashville Tennessee 37203 —
Teva Investigational Site 13541 Austin Texas 78731 —
Teva Investigational Site 13623 Dallas Texas 75214 —
Teva Investigational Site 13611 Plano Texas 75024 —
Teva Investigational Site 13572 San Antonio Texas 78229 —
Teva Investigational Site 13614 Murray Utah 84107 —
Teva Investigational Site 13581 West Jordan Utah 84088 —
Teva Investigational Site 13630 Virginia Beach Virginia 23454 —
Teva Investigational Site 13564 Seattle Washington 98105 —
Teva Investigational Site 13586 Seattle Washington 98105 —
Teva Investigational Site 13600 Morgantown West Virginia 26506 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 49 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02638103, 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 Nov 9, 2021 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02638103 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →