Overview

Long-term Safety Study of BHV-3500 (Zavegepant*) for the Acute Treatment of Migraine

Status:
Active, not recruiting
Trial end date:
2022-01-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to evaluate the long-term safety of BHV-3500/vazegepant intranasal in the acute treatment of migraine. * BHV-3500, formerly "vazegepant", is now referred to as "zavegepant" (za ve' je pant). The World Health Organization (WHO) International Nonproprietary Names (INN) Expert Committee revised the name to "zavegepant" which was accepted by the United States Adopted Names (USAN ) Council for use in the U.S. and is pending formal adoption by the INN for international use.
Phase:
Phase 2/Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Biohaven Pharmaceuticals, Inc.
Criteria
Inclusion Criteria:

- 2-8 moderate to severe migraines/month within the last 3 months

- Migraine attacks present for more than 1 year with age of onset of migraines prior to
50 years of age

- Migraine attacks, on average, lasting about 4-72 hours if untreated

- Less than 15 days with headaches (migraine or non-migraine) per month in each of the 3
months prior to the screening visit

- Ability to distinguish migraine attacks from tension/cluster headaches

- Subjects with contraindications for use of triptans may be included provided they meet
all other study entry criteria

Exclusion Criteria:

- History of HIV disease

- History of basilar or hemiplegic migraine

- Current diagnosis of major depressive disorder requiring treatment with atypical
antipsychotics, schizophrenia, bipolar disorder, or borderline personality disorder

- History of nasal surgery in the 6 months preceding the screening visit

- History of gallstones or cholecystectomy

- History of gastric, or small intestinal surgery (including Gastric Bypass, Gastric
Banding, Gastric Sleeve, Gastric Balloon, etc.), or other disease or condition (e.g.
chronic pancreatitis, ulcerative colitis, etc.) that causes malabsorption.

- BMI ≥ 33

- HbA1c ≥6.5%