Biohaven Pharmaceuticals, Inc.

An Open-label, Intermediate Size, Expanded Access Study of BHV-3000 in the Acute Treatment of Migraine

Official Title: 
BHV3000-401: An Open-label, Intermediate-size, Expanded Access Study of BHV-3000 in the Acute Treatment of Migraine
Brief Summary: 
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)
EA Type
Treatment IND/Protocol

Drug: rimegepant
rimegepant 75 mg

Eligibility Criteria: 

Inclusion Criteria:

1.Subjects who have completed any BHV3000 (rimegepant) clinical study without significant
protocol violations.

Exclusion Criteria:

1. History of basilar migraine or hemiplegic migraine

2. History with current evidence of uncontrolled, unstable or recently diagnosed cardiovascular disease

3. HIV history

4. Uncontrolled hypertension or uncontrolled diabetes

5. Current diagnosis of major depression, other pain syndromes, psychiatric conditions (e.g., schizophrenia), dementia, or significant neurological disorders (other than migraine) that, in the Investigator's opinion, might interfere with study assessments

6. History of gastric, or small intestinal surgery, or has a disease that causes malabsorption

Eligibility Gender: 
Eligibility Age: 
Minimum: 18 Years

Early Access Care

Biohaven Pharmaceuticals, Inc.
EA Number: 
Migraine prevention, phonophobia, photophobia, nausea
MeSH Terms: 
Migraine Disorders
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