A Dose-Finding Study of MK-1602 in the Treatment of Acute Migraine (MK-1602-006)

Migraine Clinical Trial

Official title:

A Phase IIb, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Dose-Finding Study of MK-1602 in the Treatment of Acute Migraine

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01613248
• Other study ID #: 1602-006
• Status: Completed
• Phase: Phase 2
• Start date: July 1, 2012
• Est. completion date: December 1, 2012

Study information

• Verified date: December 2018
• Source: Allergan
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to assess the effectiveness, safety and tolerability of a range of doses of MK-1602 versus placebo in the treatment of acute migraine.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 834
• Est. completion date: December 1, 2012
• Est. primary completion date: December 1, 2012
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• > 1 year history of migraine with or without aura as defined by International Headache Society (IHS) criteria 1.1 and/or 1.2

• Migraines typically last between 4 to 72 hours, if untreated

• = 2 and = 8 moderate or severe migraine attacks per month in each of

the two months prior to screening

• Male, female who is not of reproductive potential, or female of

reproductive potential with a screening serum ß-human chorionic gonadotropin (ß-hCG) level consistent with a not-pregnant state, and who agrees to use acceptable contraception

Exclusion Criteria:

• Pregnant or breast-feeding, or is a female expecting to conceive within the projected duration of study participation

• Participant has difficulty distinguishing his/her migraine attacks from tension-type headaches

• History of predominantly mild migraine attacks or migraines that usually

resolve spontaneously in less than two hours

• More than 15 headache-days per month or has taken medication for acute headache on more than 10 days per month in any of the three months prior to screening

• Basilar-type or hemiplegic migraine headache

• > 50 years old at age of migraine onset

• Taking migraine prophylactic medication where the prescribed daily dose

has changed during the 3 months prior to screening and will not be changed

during the study

• Taking a proton pump inhibitor (PPI) or a histamine receptor 2 (H2) blocker on a daily or near daily basis (> 3 days per week)

• Taking the following medications from 1 month prior to screening through study period:

potent cytochrome P450 (CYP) 3A4 inhibitors (e.g., cyclosporine, itraconazole, ketoconazole, fluconazole, erythromycin, clarithromycin, nefazodone, telithromycin, cimetidine, quinine, diltiazem, verapamil, and human immunodeficiency virus [HIV] protease inhibitors), moderate or marked CYP3A4 inducers (e.g., rifampicin, rifabutin, barbiturates [e.g., phenobarbital and primidone], systemic glucocorticoids, nevirapine, efavirenz, pioglitazone, carbamazepine, phenytoin, and St. Johns wort), or drugs with narrow therapeutic margins and potential for drug interactions in the CYP2C family (e.g., warfarin)

• Participant is unable to refrain from consumption of grapefruit or grapefruit juice during study

• History of hypersensitivity to, or has experienced a serious adverse event

in response to 3 or more classes of drugs (prescription and over-the-counter)

• Clinical or laboratory evidence of uncontrolled diabetes, human immunodeficiency virus (HIV) disease, or significant pulmonary, renal, hepatic, endocrine, or other systemic disease

• Other confounding pain syndromes, psychiatric conditions such as uncontrolled major depression, dementia or significant neurological disorders other than migraine. Patients who are currently being treated with non-prohibited medication for depression and symptoms are well controlled are eligible to participate

• Participant is at imminent risk of self-harm

• History of malignancy = 5 years prior to study, except for adequately treated basal cell or squamous cell skin cancer, or in situ cervical cancer

• History of gastric or small intestinal surgery (including gastric bypass

surgery or banding), or presence of a disease that causes malabsorption

• Participant has recent history (within the last year) of drug or alcohol abuse or dependence or is a user of recreational or illicit drugs

• Participant is legally or mentally incapacitated

• Donation of blood products or phlebotomy of > 300 ml within 8

weeks of study, or intent to donate blood products or receive

blood products within 30 days of screening and throughout study

• Intent to donate eggs or sperm within the projected duration of the

study

• Current participation in or participation within 30 days of screening

in a study with an investigational compound or device

• Previous exposure to MK-0974 and/or MK-3207

• Use within the past 2 months of an opioid- or barbiturate-containing

analgesic for migraine relief

• Inpatient or emergency department treatment of an acute migraine

attack within the past 2 months

Related Conditions & MeSH terms

• Migraine
• Migraine Disorders

Intervention

Drug:
• MK-1602
Single 1, 10, 25, 50 or 100 mg dose of MK-1602 taken at onset of migraine of moderate or severe intensity. Dosage form is film coated tablet for oral administration. Dose is provided to participants as a blinded bottle of tablets packaged to achieve the various MK-1602 dose levels to be studied. Participants will be instructed to take all study medication from the bottle when they treat their migraine headache.
• Placebo-matching MK-1602
Single administration of placebo-matching MK-1602 taken at onset of migraine of moderate or severe intensity. Dosage form is film coated tablet for oral administration. Dose is provided to participants as a blinded bottle of tablets packaged to achieve placebo study medication. Participants will be instructed to take all study medication from the bottle when they treat their migraine headache.
• Rescue medication
If moderate or severe migraine headache pain continues 2 hours after dose of study medication or if migraine headache comes back within 48 hours, Participants will be allowed to take their own rescue migraine medication, which may include analgesics (e.g., nonsteroidal anti-inflammatory drugs [NSAIDs]), anti-emetics, triptans or other medication not explicitly excluded.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Allergan

References & Publications (1)

Voss T, Lipton RB, Dodick DW, Dupre N, Ge JY, Bachman R, Assaid C, Aurora SK, Michelson D. A phase IIb randomized, double-blind, placebo-controlled trial of ubrogepant for the acute treatment of migraine. Cephalalgia. 2016 Aug;36(9):887-98. doi: 10.1177/0333102416653233. Epub 2016 Jun 6. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Percentage of Participants Reporting Pain Freedom (PF) at 2 Hours Post-Dose	PF was defined as a reduction in headache severity from Grade 2 or 3 at Baseline to Grade 0. Headache severity was reported by the participant using a 4-point scale where: 0=no pain, 1=mild pain, 2=moderate pain and 3=severe pain.	2 hours post-dose
Primary	Percentage of Participants Reporting Pain Relief (PR) at 2 Hours Post-Dose	PR was defined as a reduction of a moderate or severe migraine headache (Grade 2 or 3) at Baseline to a mild headache or no headache (Grade 1 or 0) 2 hours post-dose. Headache severity was reported by the participant using a 4-point scale where: 0=no pain, 1=mild pain, 2=moderate pain and 3=severe pain.	2 hours post-dose
Primary	Number of Participants With One or More Adverse Events Within 48 Hours Post-Dose	An AE is any unfavorable and unintended change in the structure (signs), function (symptoms), or chemistry (laboratory data) of the body temporally associated with any use of a sponsor product, whether or not considered related to the use of the product.	Up to 48 hours post-dose
Primary	Number of Participants With One or More Adverse Events Within 14 Days Post-Dose	An AE is any unfavorable and unintended change in the structure (signs), function (symptoms), or chemistry (laboratory data) of the body temporally associated with any use of a sponsor product, whether or not considered related to the use of the product.	Up to 14 days post-dose
Primary	Number of Participants Who Discontinued From Study Due to Adverse Events		Up to 5 weeks post-dose
Secondary	Percentage of Participants Reporting Absence of Phonophobia at 2 Hours Post-Dose	Phonophobia is sensitivity to loud sounds.	2 hours post-dose
Secondary	Percentage of Participant Reporting Absence of Photophobia at 2 Hours Post-Dose	Photophobia is sensitivity to bright light.	2 hours post-dose
Secondary	Percentage of Participants Reporting Absence of Nausea at 2 Hours Post-Dose		2 hours post-dose
Secondary	Percentage of Participants Reporting Sustained Pain Freedom (SPF) 2-24 Hours Post-Dose	SPF was defined as PF at 2 hours post-dose, with no administration of any rescue medication and with no occurrence of a mild/moderate/severe headache during the 24 hour period after dosing with study medication.	2-24 hours post-dose
Secondary	Percentage of Participants Reporting SPF 2-48 Hours Post-Dose	SPF was defined as PF at 2 hours post-dose, with no administration of any rescue medication and with no occurrence of a mild/moderate/severe headache during the 48 hour period after dosing with study medication.	2-48 hours post-dose
Secondary	Percentage of Participants Reporting Sustained Pain Relief (SPR) 2-24 Hours Post-Dose	SPR was defined as PR at 2 hours post-dose, with no administration of any rescue medication and with no occurrence of a moderate/severe headache during the 24 hour period after dosing with study medication.	2-24 hours post-dose
Secondary	Percentage of Participants Reporting SPR 2-48 Hours Post-Dose	SPR was defined as PR at 2 hours post-dose, with no administration of any rescue medication and with no occurrence of a moderate/severe headache during the 48 hour period after dosing with study medication.	2-48 hours post-dose
Secondary	Percentage of Participants Reporting Total Migraine Freedom (TMF) at 2 Hours Post-Dose	TMF at 2 hours post dose was defined as PF with no photophobia, phonophobia, nausea, or vomiting at 2 hours post-dose.	2 hours post-dose
Secondary	Percentage of Participants Reporting TMF at 2-24 Hours Post-Dose	TMF at 2-24 hours post-dose was defined as SPF with no photophobia, phonophobia, nausea, or vomiting during the 2 to 24 hour period after dosing with study medication.	2-24 hours post-dose
Secondary	Percentage of Participants Reporting TMF at 2-48 Hours Post-Dose	TMF at 2-48 hours post-dose was defined as SPF with no photophobia, phonophobia, nausea, or vomiting during the 2 to 48 hour period after dosing with study medication.	2-48 hours post-dose