A Study of Galcanezumab (LY2951742) in Participants 6 to 17 Years of Age With Episodic Migraine
REBUILD-1
A Randomized, Double-Blind, Placebo-Controlled Study of Galcanezumab in Patients 6 to 17 Years of Age With Episodic Migraine - the REBUILD-1 Study
3 other identifiers
interventional
533
10 countries
73
Brief Summary
The main purpose of this study is to evaulate the efficacy and safety of galcanezumab in participants 6 to 17 years of age for the preventive treatment of episodic migraine. The primary objective is to demonstrate the superiority of galcanezumab versus placebo in the reduction of monthly migraine headache days across the 3-month double-blind treatment period.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for phase_3
Started Mar 2018
Longer than P75 for phase_3
73 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 8, 2018
CompletedFirst Posted
Study publicly available on registry
February 14, 2018
CompletedStudy Start
First participant enrolled
March 14, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 14, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
November 1, 2026
ExpectedJanuary 26, 2026
January 1, 2026
7.7 years
February 8, 2018
January 23, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change from Baseline in the Number of Monthly Migraine Headache Days
Change from baseline in the number of monthly migraine headache days
Baseline, 3 Months
Secondary Outcomes (15)
Percentage of Participants with Reduction from Baseline ≥50%, ≥75% and 100% in Monthly Migraine Headache Days
3 Months
Change from Baseline in the Number of Monthly Migraine Headache Days with Nausea and/or Vomiting
Baseline, 3 Months
Change from Baseline in the Number of Monthly Migraine Headache Days with Photophobia and Phonophobia
Baseline, 3 Months
Change from Baseline in the Number of Monthly Migraine Headaches with Prodromal Symptoms
Baseline, 3 Months
Change from Baseline in the Number of Migraine Headache Days on which Acute Headache Medication is Taken
Baseline, 3 Months
- +10 more secondary outcomes
Study Arms (2)
Galcanezumab
EXPERIMENTALGalcanezumab administered by SQ injection. Participants may be eligible for optional open-label extension at the end of the double-blind period.
Placebo
PLACEBO COMPARATORPlacebo administered by SQ injection. Participants may be eligible for optional open-label extension at the end of the double-blind period.
Interventions
Eligibility Criteria
You may qualify if:
- Have a diagnosis of migraine with or without aura as defined by the IHS ICHD-3 guidelines (1.1 or 1.2 according to ICHD-3 \[2018\]), with a history of migraine headaches of at least 6 months prior to screening.
You may not qualify if:
- Participants who are taking, or are expected to take, therapeutic antibodies during the course of the study (adalimumab, infliximab, trastuzumab, bevacizumab, etc.). Prior use of therapeutic antibodies is allowed if that use was more than 12 months prior to baseline.
- Known hypersensitivity to monoclonal antibodies or other therapeutic proteins, or to galcanezumab or its excipients.
- Current use or prior exposure to galcanezumab, another CGRP antibody, or CGRP receptor antibody, including those who have previously completed or withdrawn from this study or any other study investigating a CGRP antibody.
- History of IHS ICHD-3 diagnosis of new daily persistent headache, cluster headache or migraine subtypes including hemiplegic (sporadic or familial) migraine and migraine with brainstem aura (previously basilar-type migraine).
- History of significant head or neck injury within 6 months prior to screening; or traumatic head injury at any time that is associated with significant change in the quality or frequency of their headaches, including new onset of migraine following traumatic head injury.
- Participants with a known history of intracranial tumors or developmental malformations including Chiari malformations.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (73)
Rehabilitation & Neurological Services
Huntsville, Alabama, 35805, United States
21st Century Neurology, a Division of Xenoscience, Inc.
Phoenix, Arizona, 85004, United States
Phoenix Children's Hospital
Phoenix, Arizona, 85016, United States
Center for Neurosciences
Tucson, Arizona, 85718, United States
Miller Children's & Women's Hospital Long Beach
Long Beach, California, 90806, United States
Wr-McCr, Llc
San Diego, California, 92108, United States
Children's Hospital Colorado
Aurora, Colorado, 80045, United States
Clinical Neuroscience Solutions, Inc. dba CNS Healthcare
Jacksonville, Florida, 32256, United States
University of Miami Don Suffer Clinical Research Building
Miami, Florida, 33136, United States
Ezy Medical Research
Miami Lakes, Florida, 33015, United States
Clinical Neuroscience Solutions
Orlando, Florida, 32801, United States
Avanza Medical Research Center
Pensacola, Florida, 32503, United States
USF Health
Tampa, Florida, 33612, United States
Premiere Research Institute at Palm Beach Neurology
West Palm Beach, Florida, 33407, United States
Clinical Integrative Research Center of Atlanta, LLC
Atlanta, Georgia, 30328, United States
Meridian Clinical Research, LLC
Savannah, Georgia, 31406, United States
Medical Research Partners
Ammon, Idaho, 83406, United States
Elite Clinical Trials
Blackfoot, Idaho, 83221, United States
Northwest Clinical Trials
Boise, Idaho, 83704, United States
Inpatient Pharmacy
Hoffman Estates, Illinois, 60169, United States
University of Kentucky Chandler Medical Center
Lexington, Kentucky, 40536, United States
Pharmasite Research, Inc.
Baltimore, Maryland, 21208, United States
Boston Clinical Trials
Boston, Massachusetts, 02131, United States
MedVadis Research Corporation
Waltham, Massachusetts, 02451, United States
Minneapolis Clinic of Neurology - Burnsville Office
Burnsville, Minnesota, 55337, United States
Children Mercy Pediatric Clinical Research Unit
Kansas City, Missouri, 64108, United States
Dent Neurologic Institute
Amherst, New York, 14226, United States
Cohen Children's Northwell Health Physician Partners - Pediatric Neurology
New Hyde Park, New York, 11042, United States
Velocity Clinical Research at Raleigh Neurology
Raleigh, North Carolina, 27607, United States
Cincinnati Children's Hospital Medical Center
Cincinnati, Ohio, 45229, United States
Providence Health & Services
Portland, Oregon, 97225, United States
UPMC Children's Hospital of Pittsburgh
Pittsburgh, Pennsylvania, 15224, United States
Office 18
Pittsburgh, Pennsylvania, 15236, United States
Velocity Clinical Research, Providence
East Greenwich, Rhode Island, 02818, United States
Tribe Clinical Research, LLC
Greenville, South Carolina, 29607, United States
Pain and Headache Centers of Texas
Houston, Texas, 77054, United States
Northwest Clinical Research Center
Bellevue, Washington, 98007, United States
Seattle Children's Hospital
Seattle, Washington, 98105, United States
Sanos Clinic - Nordjylland
Aalborg, 9362, Denmark
Herlev and Gentofte Hospital
Copenhagen, 2730, Denmark
Praxis Dr. Astrid Gendolla
Essen, 45133, Germany
Mangala Hospital & Mangala Kidney Foundation
Mangalore, 575003, India
Getwell Hospital and Research Institute
Nagpur, 440012, India
Central India Cardiology and Research Institute
Nagpur, 440015, India
All India Institute of Medical Sciences (AIIMS) - Nagpur
Nagpur, 441108, India
G.B. Pant Institute of Postgraduate Medical Education & Research
New Delhi, 110002, India
All India Institute of Medical Sciences
New Delhi, 110029, India
Sir Ganga Ram Hospital
New Delhi, 110060, India
Medipoint Hospitals Pvt. Ltd.
Pune, 411007, India
IRCCS Istituto Neurologico Carlo Besta
Milan, 20133, Italy
Ospedale Pediatrico Bambino Gesù
Roma, 00165, Italy
Policlinico Umberto I
Roma, 161, Italy
Konan Hospital
Kobe, 658-0064, Japan
Umenotsuji Clinic
Kochi, 780-8011, Japan
Tatsuoka Neurology Clinic
Kyoto, 600-8811, Japan
Yamaguchi Clinic
Nishinomiya, 663-8204, Japan
Tominaga Hospital
Osaka, 556-0017, Japan
Sendai Headache and Neurology Clinic
Sendai, 982-0014, Japan
Tokyo Medical University Hospital
Shinjuku-ku, 160-0023, Japan
Tokyo Headache Clinic
Tokyo, 151-0051, Japan
Centro de Investigacion Medica Aguascalientes (CIMA)
Aguascalientes, 20116, Mexico
Operadora Unidad de Investigación en Salud de Chihuahua S.A. de C.V.
Chihuahua City, 31203, Mexico
Hospital Civil Fray Antonio Alcalde
Guadalajara, 44280, Mexico
PanAmerican Clinical Research - Guadalajara
Guadalajara, 44670, Mexico
Clinica De Enfermedades Cronicas y Procedimientos Especiales
Morelia, 58249, Mexico
Isala, locatie Zwolle
Zwolle, 8025 AB, Netherlands
Dr. Samuel Sanchez PSC
Caguas, 727, Puerto Rico
Ponce Medical School Foundation Inc.
Ponce, 00716, Puerto Rico
Hospital Universitari Vall d'Hebron
Barcelona, 8035, Spain
Hospital de la Santa Creu i Sant Pau
Barcelona, 8041, Spain
Hospital Universitario Virgen Del Rocio
Seville, 41013, Spain
Hospital Clinico de Valencia
Valencia, 46010, Spain
Hospital Clínico Universitario de Valladolid
Valladolid, 47005, Spain
Related Links
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 8 AM - 8 PM Eastern time (UTC/GMT - 5 hours, EST)
Eli Lilly and Company
Study Design
- Study Type
- interventional
- Phase
- phase 3
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, INVESTIGATOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 8, 2018
First Posted
February 14, 2018
Study Start
March 14, 2018
Primary Completion
November 14, 2025
Study Completion (Estimated)
November 1, 2026
Last Updated
January 26, 2026
Record last verified: 2026-01
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, CSR
- Time Frame
- Data are available 6 months after the primary publication and approval of the indication studied in the US and EU, whichever is later. Data will be indefinitely available for requesting.
- Access Criteria
- A research proposal must be approved by an independent review panel and researchers must sign a data sharing agreement.
Anonymized individual patient level data will be provided in a secure access environment upon approval of a research proposal and a signed data sharing agreement.