Corabotase →PlaceboCorabotase dose ACorabotase dose B
Corabotase: Lyophilised powder
Placebo: Excipients without active substance, Lyophilised powder
Corabotase dose A: Lyophilised powder
Corabotase dose B: Lyophilised powder
Study summary
A migraine is a headache with severe throbbing pain or a pulsating sensation, usually on one side of the head. It is often accompanied by feeling or being sick and a sensitivity to bright lights and sound. Migraines are caused by a series of events when the brain gets stimulated or activated, which causes the release of chemicals that cause pain. Corabotase (also known as IPN10200) is a medication that stops the release of these chemical messengers.
Participants with episodic migraine (EM) or chronic migraine (CM) will be included in both Step 1 and Step 2. "Headache days" are when participants experience headaches that meet the criteria for a migraine or a headache without the additional migraine-specific symptoms. "Migraine days" occur when the headache displays clear migraine characteristics.
This study aims to determine:
* The safety and efficacy of injecting Corabotase directly into the muscles of the head and neck to prevent EM and CM,
* The right amount (dose) of Corabotase to inject at each point,
* The total amount (dose) of Corabotase that provides the best balance between safety and efficacy preventing migraines.
Participants will need to complete a daily electronic migraine Diary (eDiary) and questionnaires throughout the study. The total study duration for a participant will be up to 44 weeks.
Eligibility
Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria:
1. Capable of giving signed informed consent, which includes compliance with the requirements and restrictions listed in the ICF. Participant has provided written informed consent and signed privacy/data protection documentation;
2. Male or female ≥18 to 80 years of age at the time of signing the informed consent;
3. Diagnosis of either EM or CM, per ICHD-3 criteria, for at least 12 months prior to the screening visit;
4. Diagnosis of migraine at ≤50 years of age;
5. Participants in the EM group: History of EM diagnosis and headache frequency (i.e. migraine and non-migraine headache): ≤14 headache days in the 4 weeks prior to randomisation on study Day 1 based on information recorded in the eDiary; migraine frequency: ≥6 migraine days in the 4 weeks prior to randomisation on study Day 1 based on information recorded in the eDiary;
6. Participants in the CM group: History of CM diagnosis and headache frequency (i.e. migraine and non-migraine headache): ≥15 headache days in the 4 weeks prior to randomisation on study Day 1 based on information recorded in the eDiary; migraine frequency: ≥8 migraine days in the 4 weeks prior to randomisation on study Day 1 based on information recorded in the eDiary;
7. Participant with a history of use of at least one preventive treatment for migraine.
Exclusion Criteria:
1. History or current diagnosis of migraine with brainstem aura, retinal migraine, complications of migraine, tension-type headache, trigeminal autonomic cephalalgias, hypnic headache, hemicrania continua or new daily persistent headache;
2. Headache attributed to another disorder (e.g. secondary headaches), except medication overuse headache (MOH);
3. Current uncontrolled psychiatric or psychological condition, or one that could confound assessment of headaches/migraines or interfere with study participation;
4. Risk of self-harm or harm to others as evidenced by past suicidal behaviour or endorsing items 3, 4, or 5 on the C-SSRS at screening or Day 1.
5. Participants presenting with a swallowing disorder of any origin which might be exacerbated by botulinum toxin treatment, such as:
\- Grade 3 or 4 on the Dysphagia Severity Scale (severe dysphagia) with swallowing difficulties and requiring a change in diet.
6. Clinically relevant skin condition or infection that could interfere with injection of study intervention;
7. Participant has any medical condition or situation that would make them unsuitable for participation in the study;
8. Participant receiving more than one allowable concomitant migraine preventive treatment;
9. Known history of an inadequate response to \>4 medications prescribed for the prevention of migraine (2 of which have different mechanisms of action to botulinum toxin);
10. Use of any of the following medications in the specified timeframe prior to the screening visit:
* Botulinum toxin for migraine within 24 weeks (or for any other medical/aesthetic reason within 16 weeks);
* Prior use of mAbs blocking CGRP pathway within 12 weeks for preventative treatment of migraine
* Prior use of oral CGRP receptor antagonist (gepants) for preventative treatment of migraine within 2 weeks;
* Anaesthetic or steroid injection in any region targeted for treatment with study medication within 4 weeks;
* Use of cannabidiol or other types of cannabinoids within 30 days;
* Use of medical device to treat migraine within 4 weeks (e.g. non-invasive neuromodulation therapies such as nerve stimulation (gammaCore), transcranial magnetic stimulation (cephaly), external trigeminal nerve stimulation, transcutaneous electrical nerve stimulation and peripheral neuroelectrical stimulation);
* Use of other intervention to treat migraine that is assessed to interfere with study evaluations within 4 weeks (e.g. acupuncture in the head and neck region, cranial traction, nociceptive trigeminal inhibition, occipital nerve block treatments and dental splints for headache);
* Use of opioids or barbiturates for more than 2 days/month within the last 4 weeks.
11. Concurrent participation in another interventional clinical study (or within specified timeframe according to national or local legislation or requirements);
12. Diagnosis of other significant pain disorders that could confound the assessment of headaches/migraines or interfere with study participation, including but not limited to chronic pain disorders such as fibromyalgia, chronic low back pain and complex regional pain syndrome;
13. Pregnant women, nursing women, premenopausal women, or WOCBP (i.e. not surgically sterile or 1 year postmenopausal) not willing to practice an acceptable contraceptive method, at the beginning of the study and for a minimum of 12 weeks following the administration of study treatment;
14. Male subjects who are not vasectomised and who have female partners of childbearing potential and are not willing to use condoms with spermicide for a minimum of 12 weeks following the initial double-blind administration of the treatment;
15. History of alcohol or drug abuse within 5 years of the screening visit (excluding medication overuse for headache);
16. Body mass index (BMI) ≥35 kg/m² at the screening visit;
17. Known clinically significant hypersensitivity to any of the study drugs, excipients or materials used to administer the study drug;
18. Patients who, in the clinician's judgment, are actively suicidal, and therefore, deemed to be at significant risk for suicide.
19. A diagnosis of a neuromuscular disorder or respiratory disorder, such as myasthenia gravis, Lambert-Eaton syndrome or amyotrophic lateral sclerosis that in the opinion of the investigator would compromise the safety of the study participant.
Primary outcome measure(s)
Percentage of participants experiencing any Adverse Event (AEs) including treatment emergent adverse events (TEAEs), serious adverse events (SAEs), adverse event of special interest (AESI) and AE leading to treatment discontinuation — For step 1: From baseline until end of study at Week 36 An Adverse event (AE) is any untoward medical occurrence in a clinical study participant, temporally associated with the use of study intervention, whether or not considered related to the study intervention. TEAE is an AE for which the start date is on or after the date that the intervention began.
Percentage of Participants with clinically significant changes from baseline in Laboratory Parameters — For step 1: At all timepoints post injection until Week 36 Clinically significant change in laboratory parameters will be reported. The clinical significance will graded by the investigator.
Percentage of Participants With Clinically Significant Changes from baseline in Vital Signs — For step 1: At all timepoints post injection until Week 36 Clinically significant changes in vital signs will be reported. The clinical significance will be graded by the investigator.
Percentage of participants with clinically significant change from baseline in facial examination — For step 1: At all timepoints post injection until Week 36 Clinically significant changes in facial examination and focused neurological/physical examinations will be reported. The clinical significance will be graded by the investigator.
Percentage of participants with clinically significant change from baseline in 12-lead Electrocardiogram (ECG) readings — For step 1: At all timepoints post injection until Week 36
Treatment-emergence of suicidal ideation/suicidal behaviour — For step 1: At all timepoints post injection until Week 36 It will be assessed by the Columbia-Suicide Severity Rating Scale (C-SSRS) questionnaire that consists of 2 subscales:
1. Ideation severity subscale: questions answered yes/no, severity of ideation scored 1-5 with 5 being most severe
2. Intensity of ideation subscale : scores range from 2-25 with higher scores indicating more severe intensity of ideation.
Percentage of participants with Binding antibodies to IPN10200 — For step 1: At baseline, Week 4, Week 12 and Week 36.
Percentage of participants with neutralising antibodies to IPN10200 — For step 1: At baseline, Week 4, Week 12 and Week 36.
Change from baseline in the number of Monthly migraine days (MMD)s — For step 2: At Week 12 (Weeks 9-12).
Trial sites (162)
Facility
City
Region
Status
Central Research Associates
Birmingham
Alabama
Rehabilitation & Neurological Services, LLC
Huntsville
Alabama
MD First Research - Chandler - Neurology
Chandler
Arizona
MD First Research - Chandler
Chandler
Arizona
Axiom Research, LLC
Apple Valley
California
Profound Research. LLC - NCSC
Carlsbad
California
M3Wake -PRI Encino
Encino
California
WR-PRI Encino
Encino
California
Neuro-Pain Medical Center
Fresno
California
Fullerton Neurological Center - Neurology
Fullerton
California
Neurology Center of North Orange County
Fullerton
California
Kaizen Brain Center
La Jolla
California
Pharmacology Research Institute (PRI)
Los Alamitos
California
Pharmacology Research Institute (PRI) - Los Alamitos/Long Beach
Newport Beach
California
Profound Research, LLC
Pasadena
California
Acclaim Clinical Research - Internal Medicine
San Diego
California
Clinical Trials Management LLC
Thousand Oaks
California
Alliance Clinical West Hills (Focus Clinical Research)
West Hills
California
Advanced Neuroscience Research Center, LLC
Fort Collins
Colorado
Advanced Neuroscience Research Center, LLC - Neurology
Fort Collins
Colorado
New England Institute for Neurology and Headache (NEINH)/Medical Practice
Stamford
Connecticut
Neurology Offices
Boca Raton
Florida
AGA Clinical Trials
Hialeah
Florida
M3 Wake Research/MSRA, LLC
Lake City
Florida
M3 Wake Research/MSRA,LLC
Lake City
Florida
Renstar Medical Research
Ocala
Florida
Clinical Neuroscience Solutions, Inc.
Orlando
Florida
Emerald Coast Center For Neurological Disorders
Pensacola
Florida
Conquest Research
Winter Park
Florida
NeuroTrials Research, Inc.
Atlanta
Georgia
Crescent City Headache and Neurology Center, LLC
Chalmette
Louisiana
Ochsner Health Center - Covington
Covington
Louisiana
DelRicht Research
New Orleans
Louisiana
DelRicht Research at Touro Medical Center
New Orleans
Louisiana
LSU Healthcare Network Orthopedic & Sports Medicine
New Orleans
Louisiana
MedStar Neurosciences and Rehabilitation Research Network
Baltimore
Maryland
MedStar Neurosciences and Rehabilitation
Baltimore
Maryland
MedStar Franklin Square Hospital Center
Baltimore
Maryland
Medstar Franklin Square Medical Center
Baltimore
Maryland
Neurology Center of NE,PC - Neurology
Foxborough
Massachusetts
+ 122 more sites — see the full list on the official registry below.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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