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Assessment of LBR-101 In Chronic Migraine

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ClinicalTrials.gov Identifier: NCT02021773
Recruitment Status : Completed
First Posted : December 27, 2013
Last Update Posted : April 4, 2018
Sponsor:
Information provided by (Responsible Party):
Teva Pharmaceutical Industries

Study Description
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Brief Summary:
The purpose of the study is to determine whether monthly subcutaneous administration of LBR-101 is safe and provides migraine prevention in patients with chronic migraine.

Condition or disease Intervention/treatment Phase
Chronic Migraine Biological: LBR-101 High Dose Biological: LBR-101 Low Dose Biological: Placebo Phase 2

Detailed Description:
Two distinct doses of subcutaneous LBR-101 administered monthly will be compared to placebo for safety and efficacy. The mean change from baseline in the number of cumulative headache hours measured at the 28-day period ending with week 12.
Study Design
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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 277 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Prevention
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 Start Date : January 2014
Actual Primary Completion Date : February 2015
Actual Study Completion Date : March 2015

Resource links provided by the National Library of Medicine

MedlinePlus Genetics related topics: Migraine
MedlinePlus related topics: Migraine

Arms and Interventions
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Arm Intervention/treatment
Experimental: LBR-101 High Dose
Subcutaneous High Dose LBR-101 Administered Monthly x 3
 Biological: LBR-101 High Dose
Subcutaneously Administered LBR-101 Monthly x 3
Experimental: LBR-101 Low Dose
Subcutaneous Low Dose LBR-101 Administered Monthly x 3
 Biological: LBR-101 Low Dose
Subcutaneously Administered LBR-101 Monthly x 3
Placebo Comparator: Placebo
Subcutaneous Placebo Administered Monthly x 3
 Biological: Placebo
Subcutaneously Administered Placebo (Vehicle) Monthly x 3


Outcome Measures
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Primary Outcome Measures :
  1. Mean change from baseline in the number of monthly cumulative headache hours of any severity on headache days relative to the 28-day post-treatment period ending with week 12 [ Time Frame: 12 weeks after first dose of blinded study drug ]
  2. Safety as determined by the presence of Adverse events by treatment group [ Time Frame: 12 weeks after first dose of blinded study drug ]

Secondary Outcome Measures :
  1. Mean change from baseline in the number of headache days of at least moderate severity relative to the 28-day post-treatment period ending with week 12. [ Time Frame: 12 weeks after first dose of blinded study drug ]

Eligibility Criteria
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Ages Eligible for Study:   18 Years to 65 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Males or females aged 18 to 65 years of age.
  • A signed and dated informed consent document indicating that the subject has been informed of all pertinent aspects of the study including any known and potential risks and available alternative treatments.
  • Chronic migraine meeting the diagnostic criteria listed in the International Classification of Headache Disorders (ICHD-III beta version, 2013)
  • Body Mass Index (BMI) of 17.5 to 37.5 kg/m2, and a total body weight between 50 kg and 120 kg inclusive.
  • Demonstrated compliance with the electronic headache diary during the run-in period headache data on a minimum of 22/28 days (80% diary compliance)

Exclusion Criteria:

  • Onset of chronic migraine after the age of 50 years.
  • Subject has received onabotulinum toxin A for migraine or for any medical or cosmetic reasons requiring injections in the head, face, or neck during the 6 months prior to study entry.
  • Subject is using medications containing opioids (including codeine) or barbiturates (including Fiorinal®, Fioricet®, or any other combination containing butalbital) on more than 4 days per month for the treatment of migraine or for any other reason.
  • Failed > 2 medication categories or > 3 preventive medications (within two medication categories) due to lack of efficacy for prophylactic treatment of episodic or chronic migraine after an adequate therapeutic trial
  • Treatment with an investigational drug or device within 30 days of study entry or any prior exposure to a monoclonal antibody targeting the CGRP pathway.
Contacts and Locations
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Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02021773


Locations
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Sponsors and Collaborators
Teva Pharmaceutical Industries
More Information
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Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

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Responsible Party: Teva Pharmaceutical Industries
ClinicalTrials.gov Identifier: NCT02021773    
Other Study ID Numbers: LBR-101-021
First Posted: December 27, 2013    Key Record Dates
Last Update Posted: April 4, 2018
Last Verified: April 2018
Keywords provided by Teva Pharmaceutical Industries:
Headache
Migraine
Chronic Migraine
Additional relevant MeSH terms:
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Migraine Disorders
Headache Disorders, Primary
Headache Disorders
 Brain Diseases
Central Nervous System Diseases
Nervous System Diseases