A Study to Evaluate Botulinum Toxin Type A for Injection（HengLi®）for Prophylactic Treatment of Chronic Migraine

A Multi-center, Randomized, Double-blind, Placebo Parallel-Controlled Clinical Study to Evaluate the Safety and Efficacy of Botulinum Toxin Type A for Injection (HengLi ®) for Prophylactic Treatment of Chronic Migraine in Adults

A study, multi-center, randomized, double-blind, placebo parallel-controlled method, will be carried out to evaluate the safety and efficacy of Botulinum Toxin Type A for injection (HengLi®) for prophylactic treatment with chronic migraine in adults. In the core phase, two treatments of HengLi® or the placebo will be administrated (randomized at a ratio of 2:1, the target number is 288 subjects). In the extension phase, three treatments of HengLi® will be still administrated on 288 subjects recruited ever.

Study Overview

• Status: Unknown
• Conditions: Chronic Migraine
• Intervention / Treatment: Drug: Botulinum Toxin Type A for Injection; Drug: Placebo

Detailed Description

Subjects in the core phase will be randomized into two groups: Botulinum Toxin Type A (HengLi®) (155U to 195U) or placebo. Study include a 28-day baseline screening period, a 24-week core phase with 2 administrations, and a 32-week extension phase with 3 administrations .Subjects enrolled will get a e-headache-diary in recording their headache symptoms and acute headache medications.

HengLi® was administered as 31 fixed-site, fixed-dose (5U), i.m. injections across 7 specific head/neck muscle areas every 12 weeks (weeks 0, 12, 24, 36, and 48). At the investigator's discretion, up to 40 U of additional HengLi® could have been administered among 3 muscle groups (occipitalis, temporalis, or trapezius) using a protocol-defined paradigm. Hence the maximum dose per treatment cycle was 195 U over 39 sites.

Efficacy Outcome Measures should be evaluated by headache diary, HIT-6 score and MIDAS score . The primary Outcome Measure: Change from baseline in the average number of days with headache per month (The last 4 weeks during the core phase and the 4 weeks during the baseline period should be compared with the number of headache days per month on average.)

• Study Type: Interventional
• Enrollment (Anticipated): 288
• Phase: Phase 3

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 65 years (ADULT, OLDER_ADULT)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Age≥18 and ≤65, male or female;
• Subjects voluntarily sign the informed consent.
• Patients complying with the ICHD-3(β) diagnostic criteria for chronic migraine.

Exclusion Criteria:

• Females who are pregnant, nursing, or planning a pregnancy during the study period, or females of childbearing potential, not using a reliable means of contraception;
• Known allergy or sensitivity to study medication or its component;
• Subjects having accepted prophylactic treatments of migraine (e.g. propranolol, metoprolol, bisoprolol, flunarizine, valproate, topiramate, gabapentin, naproxen, aspirin, amitriptyline, candesartan, lisinopril, etc.) within the 4 weeks before screening;
• Subjects with cardiac functional insufficiency;
• Subjects with renal insufficiency (serum creatinine>1.5 times ULN);
• Subjects with hepatic diseases (ALT or AST>twice ULN);
• Subjects with systemic myoneural junction diseases (e.g. myasthenia, Eaton-Lambert syndrome, amyotrophic lateral sclerosis, etc.);
• Subjects with a history of facial palsy;
• Infection or dermatological condition at the injection sites;
• Patients with other types of migraine that do not comply with the diagnostic criteria for chronic migraine;
• Subjects ever took any type of botulinum toxin therapy in the past 6 months;
• Subjects who have used aminoglycoside antibiotics in the recent week or need to use aminoglycoside antibiotics during conduct of the clinical study;
• Subjects live with severe cognitive disorder or mental illness, outcomes will not be measured objectively;
• Subjects live with alcohol or drug abuse;
• Subjects who have been involved in other clinical studies over the 3 months prior to this study;
• Investigator's opinion that the subject has a concurrent condition(s) that may put the subject at significant risk, may confound the study results, or may interfere significantly with the conduct of the study.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: TREATMENT
• Allocation: RANDOMIZED
• Interventional Model: PARALLEL
• Masking: DOUBLE

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
ACTIVE_COMPARATOR: Botulinum Toxin Type A for Injection; Botulinum Toxin Type A is a specific formulation of a locally injected muscle relaxant whose active ingredient is botulinum toxin type A produced by clostridium botulinum A strain Hall. Excipients contain sucrose, dextran and gelatin.	Drug: Botulinum Toxin Type A for Injection; In these studies ,patients received a minimum intramuscular (IM) dose of 155 U of Botulinum Toxin Type A（HengLi®）administered to 31 injection sites across 7 head and neck muscles using a fixed-site, fixed-dose injection paradigm (each injection was 5 U in 0.1 mL). In addition, up to 40 U Botulinum Toxin Type A,administered IM to 8 additional injection sites across 3 head and neck muscles, was allowed, using a follow-the-pain approach. Thus, the minimum dose was 155 U and the maximum dose was 195 U. In the core phase, two doses of HengLi® will be injected.In the extension phase, three doses of HengLi® will be injected.; Other Names: HengLi®
PLACEBO_COMPARATOR: Placebo; The placebo does not include botulinum toxin A ,but includes sucrose, dextran and gelatin.	Drug: Placebo; In these studies, patients received placebo administered to 31 injection sites across 7 head and neck muscles using a fixed-site, fixed-dose injection paradigm (each injection was 0.1 mL). In addition, up to 0.8 mL placebo, administered IM to 8 additional injection sites across 3 head and neck muscles, was allowed, using a follow-the-pain approach. In the core phase, two doses of placebo will be injected.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change from baseline in average number of days with headache per month	The last 4 weeks during the core phase and the 4 weeks during the baseline period should be compared with the number of headache days per month on average.	Baseline (week -4 to 0) and core phase (week 21 to 24)

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
the average number of days with headache per month	Change in the average number of days with headache per month versus the baseline	Baseline and Week 4, 8, 12, 16, 20, 28, 32, 36, 40, 44, 48, 52, 56
the average frequency of headache per month	Change in the average frequency of headache per month versus the baseline	Baseline and Week 4,8,12,16,20,24,28,32,36,40,44,48,52,56
the average frequency of migraine per month	Change in the average frequency of migraine per month versus the baseline	Baseline and Week 4,8,12,16,20,24,28,32,36,40,44,48,52,56
Proportions of subjects	Proportions of subjects with a reduction in the average frequency of migraine per month≥50% and ≥30%	Baseline and Week 4,8,12,16,20,24,28,32,36,40,44,48,52,56
Change in the average frequency of needing emergency analgesics per month	The number of days with the need of emergency analgesics during the observation period divided by the number of days in the observation period and multiplied by 28. The need of emergency analgesics refers to use of analgesics in case of attacks or use of drugs in advance to prevent pain attacks.	Baseline and Week 4,8,12,16,20,24,28,32,36,40,44,48,52,56
Change in the average severity of migraine	Sum of severity scores of migraine episodes during the observation period divided by the number of migraine episodes. The severity of each migraine episode is the severity when the pain is the fiercest, expressed using VAS (0-10).	Baseline and Week 4,8,12,16,20,24,28,32,36,40,44,48,52,56
Change in the average duration of migraine	Sum of durations of migraine episodes during the observation period divided by the number of migraine episodes.	Baseline and Week 4,8,12,16,20,24,28,32,36,40,44,48,52,56
Migraine Disability Assessment Questionnaire score(MIDAS)	Change in the MIDAS per month versus the baseline	Week 0,12,24,36,48,56
Headache Impact Test (HIT)	Change in the HIT per month versus the baseline	Week0,4,8,12,16,20,24,28,32,36,40,44,48,52,56

Collaborators and Investigators

• Sponsor: Lanzhou Institute of Biological Products Co., Ltd
• Investigators: Study Director: Sheng yuan Yu, The General Hospital of People's Liberation Army(301 hospital)

Study record dates

Study Major Dates

• Study Start: September 1, 2014
• Primary Completion (ANTICIPATED): December 1, 2019
• Study Completion (ANTICIPATED): June 1, 2020

Study Registration Dates

• First Submitted: November 11, 2014
• First Submitted That Met QC Criteria: November 13, 2014
• First Posted (ESTIMATE): November 14, 2014

Study Record Updates

• Last Update Posted (ACTUAL): January 3, 2018
• Last Update Submitted That Met QC Criteria: January 1, 2018
• Last Verified: January 1, 2018

More Information

Terms related to this study

• Keywords: Chronic Migraine; Botulinum Toxin Type A for Injection
• Additional Relevant MeSH Terms: Brain Diseases; Central Nervous System Diseases; Nervous System Diseases; Headache Disorders, Primary; Headache Disorders; Migraine Disorders; Physiological Effects of Drugs; Neurotransmitter Agents; Molecular Mechanisms of Pharmacological Action; Peripheral Nervous System Agents; Cholinergic Agents; Membrane Transport Modulators; Acetylcholine Release Inhibitors; Neuromuscular Agents; Botulinum Toxins; Botulinum Toxins, Type A; abobotulinumtoxinA
• Other Study ID Numbers: HengLi003

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO