Condition: Migraine · Acute Treatment of Migraine · Sponsor: Pfizer
Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.
The primary purpose of this study is to evaluate the efficacy of rimegepant (BMS-927711) compared with placebo in the acute treatment of migraine as measured by Pain Freedom (headache pain intensity level reported as "no pain") at 2 hours post dose using a four point numeric rating scale (no pain, mild pain, moderate pain, severe pain) while identifying an optimal dose to support the Phase 3 clinical trials.
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
Key Inclusion Criteria: * Patient with at least 1-year history of migraines (with or without aura) including the following: * Migraine attacks more than 1 year with age of onset prior to 50 years of age * Migraine attacks, on average, last about 4 - 72 hours if untreated * No more than 8 attacks of moderate to severe intensity per month within last 3 months * Patient must be able to distinguish migraine attacks from tension/cluster attacks and must have consistent migraine headaches of at least 2 migraine headaches attacks of moderate to severe intensity in each of the last 3 months * Less than 15 days of headache (migraine or non-migraine) per month in each of 3 months prior to screening * Male and female ≥ 18 years and ≤ age 65 * No clinically significant abnormality identified on the medical or laboratory evaluation Key Exclusion Criteria: * Patient has a history of basilar migraine or hemiplegic migraine * Patient does not receive migraine relief from triptan migraine treatment * Medications that may alter the pH of the stomach (acid reducing agents), such as H-2 antagonists, Proton Pump inhibitors (PPI), antacids * History of ergotamine or triptan intake greater than/equal 10 days per month on a regular basis for greater than 3 months * History of non-narcotic analgesic intake on greater then/equal 15 days per month for greater than/equal 3 months
Reproduced word-for-word from the public registry record — the study team can answer questions about it.
| Mayo Clinic Arizona | Scottsdale, Arizona, United States | — |
| Clinical Res. Advantage Inc/ Desert Clinical Research Llc | Tempe, Arizona, United States | — |
| University Of California, San Francisco | San Francisco, California, United States | — |
| California Medical Clinic For Headache | Santa Monica, California, United States | — |
| Encompass Clinical Research | Spring Valley, California, United States | — |
| Diablo Clinical Research, Inc. | Walnut Creek, California, United States | — |
| Radiant Research, Inc. | Denver, Colorado, United States | — |
| Miami Research Associates | Miami, Florida, United States | — |
| Renstar Medical Research | Ocala, Florida, United States | — |
| Compass Research, Llc | Orlando, Florida, United States | — |
| Broward Research Group | Pembroke Pines, Florida, United States | — |
| Comprehensive Clinical Development, Inc | St. Petersburg, Florida, United States | — |
+ 29 more locations — full list on the registry record.
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