Safety and Efficacy of Oral Idebenone for Preventive Treatment of Migraine in Adult Migraine Patients

NCT ID: NCT05411978

Last Updated: 2022-06-23

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE4
• Total Enrollment: 900 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-05-09
• Study Completion Date: 2024-06-20

Brief Summary

This is a multi-center, prospective, double-blind randomized controlled trial on a sample of patients with migraine. Subjects will only be enrolled when a physician or research assistant who is familiar with the study protocol is available to enroll patients. Written, informed consent will be obtained from each patient. Consent will include a discussion of the risks and benefits.

Conditions

Migraine

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: DOUBLE

Study Groups

Idebenone 30 mg+ Placebo 60 mg

Idebenone 30 mg+ placebo 60 mg TID Oral ,for 12 weeks

Group Type: PLACEBO_COMPARATOR

Idebenone+ placebo

Intervention Type: DRUG

Participants will receive Idebenone 30 mg+ placebo 60 mg for 12 weeks.

Idebenone 90 mg

Idebenone 90 mg TID Oral ,for 12 weeks

Group Type: EXPERIMENTAL

Idebenone

Intervention Type: DRUG

Participants will receive Idebenone 90 mg for 12 weeks.

Placebo 90 mg

Placebo 90 mg TID Oral,for 12 weeks

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Participants will receive Placebo 90 mg for 12 weeks

Interventions

Idebenone+ placebo

Participants will receive Idebenone 30 mg+ placebo 60 mg for 12 weeks.

Intervention Type: DRUG

Idebenone

Participants will receive Idebenone 90 mg for 12 weeks.

Intervention Type: DRUG

Placebo

Participants will receive Placebo 90 mg for 12 weeks

Intervention Type: DRUG

Other Intervention Names

Idebenone 30 mg+ placebo 60 mg; Idebenone 90 mg; Placebo 90 mg

Eligibility Criteria

Inclusion Criteria

• Male or female participants ages 18 to 65 years;
• At least a 1-year history of migraine with or without aura is consistent with a diagnosis according to the ICHD-3;
• Migraine onset before age 50 years;
• History of 4 to 15 migraine attacks days per month in each of the 3 months prior to the screening visit;
• The number of headache attacks <15 days/month during the 3 months prior to the screening visit;
• Be willing to use effective contraception during the trial and for 28 days after the end of the last dose;
• Sign the informed consent form.
• History of 4 to 14 migraine attacks days within 4 weeks during the screening visit.
• The number of headache attacks <14 days/month within 4 weeks during the screening visit;
• Completed at least 23 days of the electronic diary within 28 days during the screening visit. And the participant is to be able to read, understand and complete the study questionnaire and headache diary;
• Understand and comply with the study procedures and methods, and voluntarily participate in this study.

Exclusion Criteria

• Participants diagnosed with probable migraine by ICHD-3
• Current or previous diagnosis of primary, secondary, or painful cranial neuropathy other than migraine (diagnostic criteria according to ICHD-3)
• Prior ineffectiveness after adequate treatment with more than 2 medications, which are listed below: Divalproex, sodium valproate; topiramate; beta-blockers; Tricyclic antidepressants; serotonin-norepinephrine reuptake inhibitors; Flunarizine, Verapamil; Lisinopril, Candesartan.

Definition of failure to treat: frequency, duration, and severity of headache 6 weeks after administration of the degree of the above drug does not decrease.

• Use of other devices or prohibited medications such as painkillers containing opioids for the treatment of migraine within 2 months before or during the screening visit
• Therapeutic injections of Botulinum toxin in the head, face, or neck within 4 months before screening and during the study periods
• Simultaneous use of 2 or more drugs within 2 months before or during the screening visit may be prophylactic Medications for migraine effects (if used only 1 prophylactic drug, the dose must be stable for 2 months before the screening visit and throughout the study period)
• The following situations occur within 2 months before the screening period begins: take ergotamines or triptans at least 10 days per month, or take non-steroidal anti-inflammatory drugs (NSAID) only every month ≥15 days, NSAID combination ≥10 days, or use opioid or barbiturate analgesics ≥4 days per month;
• Participants use the prohibited drugs such as painkillers containing opioids, devices, or regimens during treatment.
• History of active chronic pain syndrome (e.g., fibromyalgia, chronic pelvic pain, face Pain, etc.);
• History of mental illness (e.g., schizophrenia or bipolar disorder) or Patient Health Questionnaire (PHQ-9) score ≥15. If the participant has a history of anxiety or depression (PHQ-9 score < 15) and takes no more than one psychotropic drug, the participant will be allowed to enter. (participant must take a steady dose of treatment within 3 months before the screening visit)
• Severe neurological disorders other than migraines (including febrile seizures);
• History of a malignant tumor within 5 years before the screening visit, except for non-melanoma skin cancer, cervical or ductal carcinoma in situ;
• The screening visit meets any of the following laboratory test values: Alanine transaminase (ALT) or aspartate aminotransferase(AST) >1.5×ULN, or total bilirubin >1.5×ULN (except for participants diagnosed with Gilbert syndrome);
• History of myocardial infarction, stroke, or transient ischemic attack, unstable angina or coronary bypass surgery within 12 months before the screening visit
• Expose participants to significant risk or confuse the study
• Based on clinical interviews or C-SSRS, the investigator believes that the subject has self-harmed or harmed him Human risk;
• History of drugs or alcohol abuse within 12 months before the screening visit
• Pregnant, planning pregnancy, or Lactating women;
• Fertile female participants are unwilling to use an effective contraceptive during the study period Method.

Infertile women as follows: history of menopause, age ≥ 55 years, menopause ≥12 months.

Age < 55 years, free from spontaneous menstruation for at least 2 years. Age < 55, has spontaneous menstruation in the past 1 year, but currently amenorrhea (e.g., Spontaneous or secondary to hysterectomy), and postmenopausal gonadotropin levels gonadotropin Luteinizing hormone (LH), follicle-stimulating Hormone> 40 IU/L or postmenopausal estradiol level <5 ng/dL History of bilateral oophorectomy, hysterectomy, or bilateral salpingectomy

• Participated in other clinical trials within the first 3 months
• Known allergy to Idebenone or any of its ingredients(e.g., lactose intolerant)；
• The participants are employees or immediate family members of the research center (parents, spouses, siblings, or children).

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Beijing Tiantan Hospital

OTHER

Sponsor Role: lead

Responsible Party

Yonggang.wang

Director

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Yonggang Wang

Beijing, , China

Site Status: RECRUITING

Countries

China

Central Contacts

YONGGANG WANG

Role: CONTACT

w100yg@163.com

15010066622

YAQING ZHANG

Role: CONTACT

Zhyq0401@126.com

13910760399

Facility Contacts

Yonggang Wang

Role: primary

w100yg@163.com

Other Identifiers

ADBK-3101-303-002

Identifier Type: -

Identifier Source: org_study_id