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ubrogepant

Generic: UBROGEPANT·Brand: UBRELVY, Ubrelvy

ubrogepant: developed by 1 company · 4 clinical trials tracked · 1 FDA decision.

ubrogepant evidence translation

What we can confirm

1 FDA record · 4 tracked trials

What it means

Source-backed records connect ubrogepant to ABBV; that link alone does not prove the drug works.

What to watch

Watch active trials and any change in FDA or trial status.
BioSniper AIPage evidence connected

Prepared research question

How could ubrogepant → ABBV affect its developer, and what evidence supports the link?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence4 indications · 1 study sponsors

Related indications

Development Pipeline (1)
CompanyPhase
AbbVie Inc. (ABBV)
Migraine; Healthy Volunteer
Phase 3
Clinical Trials (4)

A Two-Part, Phase 1, Open-Label, Randomized Study to Evaluate the Relative Bioavailability (Versus Immediate Release Tablet) and Food Effect of a New Orally Disintegrating Tablet Formulation of Ubrogepant in Healthy Volunteers

NCT07680686·Phase 1·ABBV
Recruiting

Primary endpoint: Number of Participants Experiencing Adverse Events

InterventionalRandomizedopen52 targetStarted 2026-07Completion 2026-101 site · United StatesAbbVie

A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Tolerability of Ubrogepant for the Preventive Treatment of Menstrual Migraine With an Open-Label Extension

NCT06417775·Phase 3·ABBV
Active, not recruiting

Primary endpoint: Change From Baseline in Number of Migraine Days Occurring During Perimenstrual Periods (PMPs) Across the Double-Blind Treatment Period

InterventionalRandomizedquadruple496 targetStarted 2024-09Completion 2027-1150 sites · United StatesAbbVie

Migraine Medication Effects on Urinary Symptoms

Enrolling by invitation

Primary endpoint: changes in OAB symptoms

Observational200 targetStarted 2024-04Completion 2026-121 site · United StatesThe Cleveland Clinic

A Phase 3, Multicenter, Randomized, Double-blind, Placebo-controlled, Single-attack Study to Evaluate the Efficacy, Safety, Tolerability, and Pharmacokinetics of Oral Ubrogepant in the Acute Treatment of Migraine With or Without Aura in Children and Adolescents (Ages 6-17)

NCT05125302·Phase 3·ABBV
Recruiting

Primary endpoint: Percentage of participants with Pain Freedom at 2 Hours After the Initial Dose in pediatric participants aged 6 to 17 years

InterventionalRandomizedtriple1,059 targetStarted 2022-01Completion 2027-0550 sites · United StatesAbbVie
FDA Decisions1 records
NDA211765Type 1 - New Molecular EntityStandardOralTablet

Frequently asked questions

Who is developing ubrogepant?

ubrogepant is being developed by AbbVie Inc..

How many clinical trials involve ubrogepant?

BioSniper tracks 4 clinical trials involving ubrogepant.

What is ubrogepant's latest FDA decision?

The most recent tracked FDA decision for ubrogepant is Approval, dated December 23, 2019.