Last updated: 11/04/2018 13:00:54
A Study of Combination Product (sumatriptan succinate and naproxen sodium) in Migraine Subjects Who Report Poor Response or Intolerance to Short Acting Triptans (Study 2 of 2)
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: A Study of Combination Product (sumatriptan succinate and naproxen sodium) in Migraine Subjects Who Report Poor Response or Intolerance to Short Acting Triptans (Study 2 of 2)
Trial description: This is a randomized, double-blind, placebo-controlled, crossover, two-attack, out-patient, early-intervention evaluation of subjects who have migraine with or without aura and who discontinued use of short acting triptan(s) within the past year due to non-response or intolerance. Subjects will treat 2 separate migraine attacks during the mild phase of each attack; one attack will be treated with one tablet of the Combination Product (sumatriptan succinate and naproxen sodium) and the other attack with one tablet of placebo (crossover design). [Study 2 of 2]
Primary purpose:
Treatment
Trial design:
Crossover Assignment
Masking:
Double (Participant, Investigator)
Allocation:
Randomized
Primary outcomes:
Sustained Freedom From Migraine Pain between 2-24 hours post-dose
Timeframe: 2 - 24 Hours Post-Dose
Secondary outcomes:
Migraine Headache Pain Free at 2 Hours Post-Dose
Timeframe: 2 Hours Post-Dose
Rescue Medication Use During 0 - 24 Hours Post-Dose
Timeframe: 0-24 Hours Post-Dose
Migraine Headache Pain Free at 0.5, 1, 4, and 8 Hours Post-Dose
Timeframe: 0.5, 1, 4, and 8 Hours Post-Dose
Sustained Freedom from Migraine
Timeframe: 2 - 24 hours post-dose
Migraine-Free Assessment at 2, 4, and 8 hours Post-dose
Timeframe: 2, 4 , and 8 hours post-dose
Sustained Freedom From Migraine-Associated Sinus Pain
Timeframe: 2 - 24 hours post-dose
Migraine-Associated Sinus Pain Assessed at Baseline, 2, 4, and 8 hours Post-dose
Timeframe: Baseline, 2, 4, and 8 hours post-dose
Sustained Freedom from Migraine-Associated Neck Pain
Timeframe: 2 - 24 hours post-dose
Migraine-Associated Neck Pain Assessed at Baseline, 2, 4, and 8 hours Post-dose
Timeframe: Baseline, 2, 4, and 8 hours post-dose
Sustained Freedom from Migraine-Associated Photophobia
Timeframe: 2 - 24 hours post-dose
Migraine-Associated Photophobia Assessed at Baseline, 2, 4, and 8 hours Post-dose
Timeframe: Baseline, 2, 4, and 8 hours post-dose
Sustained Freedom from Migraine-Associated Phonophobia
Timeframe: 2 - 24 hours post-dose
Migraine-Associated Phonophobia Assessed at Baseline, 2, 4, and 8 hours Post-dose
Timeframe: Baseline, 2, 4, and 8 hours post-dose
Sustained Freedom from Migraine-Associated Nausea
Timeframe: 2 - 24 hours post-dose
Migraine-Associated Nausea Assessed at Baseline, 2, 4, and 8 hours Post-dose
Timeframe: Baseline, 2, 4, and 8 hours
Sustained Complete Pain/Symptom-Free
Timeframe: 2 - 24 hours post-dose
Complete Pain/Symptom-Free Assessed at Baseline, 2, 4, and 8 hours Post-dose
Timeframe: Baseline, 2, 4, and 8 hours post-dose
Recurrence of Any Migraine Headache Pain
Timeframe: 24 hours and 48 hours
Interventions:
Enrollment:
169
Primary completion date:
2007-15-11
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Mathew N, Landy S, Tietjen G, Stark S, Runken M, Lener S, Derosier F, and Bukenya D. Evaluation of a single fixed-dose tablet of Sumatriptan 85 mg formulated with RT Technology/Naproxen sodium 500 mg (SumaRT/Nap) in Subjects who Reported Poor Response or Intolerance to Short Acting Triptans for the Acute Treatment of Migraine. Headache 2008: S44-45.
Mathew NT, Landy S, Stark S, Tietjen GE, Derosier FJ, White J, Lener SE, Bukenya D. Fixed-dose sumatriptan and naproxen in poor responders to triptans with a short half-life. Headache 2009; 49:971-982 (DOI:10.1111/j.1526-4610.2009.01458.x).
Medical condition
Migraine Disorders
Product
sumatriptan
Collaborators
Not applicable
Study date(s)
December 2006 to November 2007
Type
Interventional
Phase
3
Participation criteria
Sex
Female & Male
Age
18 - 65 years
Accepts healthy volunteers
No
- Subject is male or female between 18 and 65 years old.
- Subject has migraine with or without aura (2004 ICHD-II criteria).
- Subjects with any of the following criteria may not enroll in the study:
- Subject has non-migraine headache, retinal migraine, basilar or hemiplegic migraine, cluster headache, or headaches secondary to trauma, cranial or cervical disorders, infections, alterations of homeostasis, ENT disorders, psychiatric disorders or cranial neuralgias.
Inclusion and exclusion criteria
Inclusion criteria:
- Subject is male or female between 18 and 65 years old.
- Subject has migraine with or without aura (2004 ICHD-II criteria).
- Subject has 1-8 migraines per month over the previous 3 months and less than 15 total headache days per month.
- Subject has recently (within 1 year) discontinued the use of eletriptan, rizatriptan, sumatriptan, almotriptan, or zolmitriptan, due to nonresponse or intolerable adverse events. Non-response is defined as documented discontinuation of treatment with eletriptan, rizatriptan, sumatriptan, almotriptan, or zolmitriptan for reasons related to response, including (but not limited to): slow onset of efficacy, inconsistent efficacy, inadequate overall efficacy, or inadequate sustained efficacy through 24 hours. Intolerance is defined as documented discontinuation of treatment with eletriptan, rizatriptan, sumatriptan, almotriptan, or zolmitriptan for other reasons, attributable to the triptan, outside of non-response. A female is eligible to enter and participate in this study if she is of:
- non-childbearing potential (i.e., physiologically incapable of becoming pregnant); or,
- child-bearing potential, has a negative urine pregnancy test at screen, and agrees to one of the following acceptable measures of contraception:
- Complete abstinence from intercourse from 2 weeks prior to administration of the investigational product, throughout the study, and for a time interval after completion or premature discontinuation from the study to account for elimination of the investigational drug (a minimum of 5 days); subjects utilizing this method must agree to use an alternate method of contraception if they should become sexually active and will be queried on whether they have been abstinent in the preceding 2 weeks when they present to the clinic for the Final Visit; or,
- Female sterilization; or,
- Sterilization of male partner; or,
- Implants of levonorgestrel; or,
- Injectable progestogen; or,
- Oral contraceptive (combined or progestogen only); or,
- Any intrauterine device (IUD) with published data showing that the highest expected failure rate is less than 1% per year (not all IUDs meet this criterion); or,
- Spermicide plus a mechanical barrier (e.g., spermicide plus a male condom or a female diaphragm); or,
- Any other methods with published data showing that the highest expected failure rate for that method is less than 1% per year; or,
- Any other barrier methods only if used in combination with any of the above acceptable methods.
- Subject taking oral contraceptives has been on a stable regimen for at least 2 months prior to screening.
- Subject is willing and able to provide informed consent prior to entry into this treatment phase of the study.
- Subject is able to understand and complete the diary card.
Exclusion criteria:
- Subjects with any of the following criteria may not enroll in the study:
- Subject has non-migraine headache, retinal migraine, basilar or hemiplegic migraine, cluster headache, or headaches secondary to trauma, cranial or cervical disorders, infections, alterations of homeostasis, ENT disorders, psychiatric disorders or cranial neuralgias.
- Subject has confirmed or suspected ischemic heart disease (angina pectoris, history of myocardial infarction, documented silent ischemia), Prinzmetal’s angina/coronary vasospasm, or signs/symptoms consistent with any of the above.
- Subject has evidence or history of ischemic abdominal syndromes, peripheral vascular disease or Raynaud’s Syndrome.
- Subject has cardiac arrhythmias requiring medication or a history of a clinically significant electrocardiogram abnormality that, in the investigator’s opinion, contraindicates participation in this study.
- Subject has a history of cerebrovascular pathology including stroke and/or transient ischemic attacks (TIAs).
- Subject has a history of congenital heart disease.
- Subject has uncontrolled hypertension at screening (sitting systolic pressure ≥140mmHg, diastolic pressure ≥90mmHg).
- Subject, in the investigator’s opinion, is likely to have unrecognized cardiovascular or cerebrovascular disease (based on history or the presence of risk factors including but not limited to, hypertension, hypercholesterolemia, smoker, obesity, diabetes, strong family history of coronary artery disease, female with surgical or physiological menopause, or male over 40 years of age).
- Subject has a history of epilepsy or structural brain lesions which lower the convulsive threshold or treated with an antiepileptic drug for seizure control within 5 years prior to screening.
- Subject has a history of impaired hepatic or renal function that, in the investigator’s opinion, contraindicates participation in this study.
- Subject is currently taking a monoamine oxidase inhibitor (MAOI), or has taken a MAOI within 2 weeks prior to screening or plans to take within 2 weeks after treatment.
- Subject is currently taking, or has taken in the previous three months, a migraine prophylactic medication containing methysergide or dihydroergotamine; or is taking a medication that is not stabilized (i.e. change of dose within the past 2 months) for either chronic or intermittent migraine prophylaxis or for a co-morbid condition that is not stabilized..
- Subject is currently taking any anti-coagulant (e.g., warfarin).
- Subject has a recent history of regular use of opioids or barbiturates for treatment of their migraine headache and/or other non-migraine pain. Regular use is defined as an average of 4 days per month over the last 6 months.
- Subject is currently taking or has taken in the previous 4 weeks, herbal preparations containing St. John’s Wort (Hypericum perforatum).
- Subject has hypersensitivity, intolerance, or contraindication to the use of sumatriptan or naproxen sodium or any of their components or any other 5-HT1 receptor agonist.
- Subject has a history of allergic reactions to naproxen preparations, including subject in whom aspirin or other NSAID drugs induce the syndrome of asthma, rhinitis, and nasal polyps.
- Subject has a history of any gastrointestinal surgery that specifically indicates a past history of bleeding, ulceration or perforation.
- Subject has a history of gastric bypass or stapling surgery.
- Subject has a history of GI ulceration in the past six months or gastrointestinal bleeding in the past year.
- Subject has a history of inflammatory bowel disease.
- Subject has a history of any bleeding disorder.
- Subject is taking any antiplatelet agent (except low-dose aspirin ≤ 325mg/day for cardioprotective reasons).
- Subject is taking any angiotensin-converting enzyme (ACE) inhibitor or angiotensin receptor blocker.
- Subject is pregnant, actively trying to become pregnant or breast-feeding.
- Subject has evidence of alcohol or substance abuse within the last year which, in the investigator’s judgment, will likely interfere with the study conduct, subject cooperation, or evaluation and interpretation of the study results.
- Subject has any concurrent medical or psychiatric condition which, in the investigator’s opinion, may affect the interpretation of efficacy and safety data or which otherwise contraindicates participation in this clinical trial.
- Subject has participated in an investigational drug trial within the previous four weeks or plans to participate in another study at any time during this study.
Trial location(s)
Location
GSK Investigational Site
Toledo, Ohio, United States, 43614-5809
Status
Study Complete
Location
GSK Investigational Site
Nashville, Tennessee, United States, 37203
Status
Study Complete
Location
GSK Investigational Site
Allentown, Pennsylvania, United States, 18103
Status
Study Complete
Location
GSK Investigational Site
Philadelphia, Pennsylvania, United States, 19107
Status
Study Complete
Location
GSK Investigational Site
Williamsville, New York, United States, 14221
Status
Study Complete
Showing 1 - 6 of 28 Results
Study documents
Clinical study report
Available language(s): English
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Results posted on ClinicalTrials.gov
Recruitment status
Study complete
Actual primary completion date
2007-15-11
Actual study completion date
2007-15-11
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
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