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Completed Phase 2 Interventional Results available

A Study to Test if Fremanezumab Reduces Headache in Participants With Posttraumatic Headache (PTH)

ClinicalTrials.gov ID: NCT03347188

Public ClinicalTrials.gov record NCT03347188. 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 25, 2026, 4:00 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 Phase 2, Multicenter, Randomized, Proof-of-Concept, Double-Blind, Placebo-Controlled, Parallel-Group Study, Including an Open-Label Period, Evaluating the Efficacy and Safety of 1 Subcutaneous Dose Regimen of Fremanezumab for the Treatment of Posttraumatic Headache (PTH)

Study identification

NCT ID
NCT03347188
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Teva Branded Pharmaceutical Products R&D, Inc.
Industry
Enrollment
87 participants

Conditions and interventions

Interventions

  • Fremanezumab Drug
  • Placebo Drug

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
Dec 17, 2017
Primary completion
Mar 12, 2020
Completion
Jun 2, 2020
Last update posted
Dec 12, 2022

2017 – 2020

United States locations

U.S. sites
33
U.S. states
18
U.S. cities
32
Facility City State ZIP Site status
Teva Investigational Site 14065 Phoenix Arizona 85018
Teva Investigational Site 14069 Scottsdale Arizona 85259-5452
Teva Investigational Site 14048 Little Rock Arkansas 72205
Teva Investigational Site 30236 Little Rock Arkansas 72205
Teva Investigational Site 14052 Long Beach California 90806
Teva Investigational Site 14053 Los Angeles California 90073
Teva Investigational Site 14060 San Diego California 92161
Teva Investigational Site 14054 San Francisco California 94109
Teva Investigational Site 14045 Fairfield Connecticut 06824
Teva Investigational Site 14063 Miami Florida 33136
Teva Investigational Site 14041 North Miami Florida 33161
Teva Investigational Site 14056 Tampa Florida 33609
Teva Investigational Site 14057 Riverwoods Illinois 60015
Teva Investigational Site 14067 Indianapolis Indiana 46256
Teva Investigational Site 14058 Louisville Kentucky 40207
Teva Investigational Site 14061 Waltham Massachusetts 02451
Teva Investigational Site 14051 Kansas City Missouri 64128-2226
Teva Investigational Site 14043 Springfield Missouri 65810
Teva Investigational Site 14046 St Louis Missouri 63141
Teva Investigational Site 14119 Albany New York 12208
Teva Investigational Site 14229 Amherst New York 14226
Teva Investigational Site 14047 New York New York 10021
Teva Investigational Site 14118 The Bronx New York 10467
Teva Investigational Site 14114 Durham North Carolina 27713
Teva Investigational Site 14059 Salisbury North Carolina 28144
Teva Investigational Site 14049 Portland Oregon 97225
Teva Investigational Site 14064 Philadelphia Pennsylvania 19107
Teva Investigational Site 14040 Pittsburgh Pennsylvania 15236
Teva Investigational Site 14230 Nashville Tennessee 37203
Teva Investigational Site 14055 Dallas Texas 75390-8565
Teva Investigational Site 14050 Waco Texas 76711
Teva Investigational Site 14113 Spokane Washington 99202
Teva Investigational Site 14044 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.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03347188, 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 12, 2022 · Synced Jun 25, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03347188 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →