Ozmosi | Ubrogepant Drug Profile
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Ubrogepant

Alternative Names: ubrogepant, mk-1602, ubrelvy
Clinical Status: Active
Latest Update: 2025-10-24
Latest Update Note: Clinical Trial Update

Product Description

Ubrogepant is an oral, small-molecule calcitonin gene-related peptide receptor antagonist for acute migraine treatment. (Sourced from: https://pubmed.ncbi.nlm.nih.gov/31800988/)

Mechanisms of Action: CGRP Antagonist

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: *

Approval Status: Approved

Approved Countries: Israel | Saudi Arabia | United Arab Emirates | United States

Approved Indications: None

Known Adverse Events: None

Company: AbbVie
Company Location: Eastern America
Company CEO: Richard A. Gonzalez
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Ubrogepant

Countries in Clinic: Puerto Rico, United States

Active Clinical Trial Count: 4

Recent & Upcoming Milestones

Highest Development Phases

Phase 3: Migraine Disorders

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT05125302

Ubro Peds

P3

Recruiting

Migraine Disorders

2026-05-01

24%

2025-01-03

Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments

NCT06578585

20527A

P1

Completed

Migraine Disorders

2025-07-11

50%

2025-10-15

Patient Enrollment|Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments|Trial Status

NCT05127954

UBRO PEDS OLE

P3

Enrolling by invitation

Migraine Disorders

2028-01-01

64%

2025-07-22

Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments

NCT06417775

UBRO MM

P3

Recruiting

Migraine Disorders

2027-06-01

38%

2025-10-28