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The purpose of this protocol is to allow subjects who completed any BHV3000 (rimegepant) clinical study to continue to have access to rimegepant while collecting ongoing safety data.
(NOTE: ONLY FOR PATIENTS who participated in a previous BHV-3000/Rimegepant Clinical Trial in the past)
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| rimegepant | Drug | rimegepant 75 mg |
Inclusion Criteria:
1.Subjects who have completed any BHV3000 (rimegepant) clinical study without significant protocol violations.
Exclusion Criteria:
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| ID | Term |
|---|---|
| D008881 | Migraine Disorders |
| D012001 | Hyperacusis |
| D020795 | Photophobia |
| D009325 | Nausea |
| ID | Term |
|---|---|
| D051270 | Headache Disorders, Primary |
| D020773 | Headache Disorders |
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
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| ID | Term |
|---|---|
| C578443 | rimegepant sulfate |
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| D009422 | Nervous System Diseases |
| D006311 | Hearing Disorders |
| D004427 | Ear Diseases |
| D010038 | Otorhinolaryngologic Diseases |
| D012678 | Sensation Disorders |
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D014786 | Vision Disorders |
| D005128 | Eye Diseases |
| D012817 | Signs and Symptoms, Digestive |