ACHIEVE I STUDY

DEMONSTRATED RAPID RELIEF OF MIGRAINE PAIN VS. PLACEBO

2 hours after an initial dose of UBRELVY 100 mg, significantly more patients reported a reduction in headache severity from moderate or severe pain to mild pain or no pain vs. placebo.1,2†

DEMONSTRATED FREEDOM FROM MIGRAINE PAIN VS. PLACEBO

2 hours after an initial dose, 21.2% of patients receiving UBRELVY 100 mg reported migraine pain freedom vs. 11.8% of patients receiving placebo (co-primary endpoint; p=0.0001).1,2§‡  

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DEMONSTRATED RAPID RELIEF OF MIGRAINE PAIN VS. PLACEBO

2 hours after an initial dose of UBRELVY 100 mg, significantly more patients reported a reduction in headache severity from moderate or severe pain to mild pain or no pain vs. placebo.1,2†

DEMONSTRATED FREEDOM FROM MIGRAINE PAIN VS. PLACEBO

2 hours after an initial dose, 21.2% of patients receiving UBRELVY 100 mg reported migraine pain freedom vs. 11.8% of patients receiving placebo (co-primary endpoint; p=0.0001).1,2§‡  

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SAFETY INFORMATION

Click here for additional safety information and for a link to the Product Monograph discussing:

Contraindications with concomitant use of strong CYP3A4 inhibitors.

Relevant warnings and precautions regarding driving and operating machinery, hypersensitivity reactions, may reduce effectiveness of oral contraceptives, use in pregnant or breast-feeding women and dose selection in geriatric patients.

Conditions of clinical use, adverse reactions, drug interactions and dosing instructions.

 

FOR MORE INFORMATION

For any questions related to UBRELVY, you can contact AbbVie Medical Information at 1-844-241-5011

SAFETY INFORMATION

Click here for additional safety information and for a link to the Product Monograph discussing:

Contraindications with concomitant use of strong CYP3A4 inhibitors.

Relevant warnings and precautions regarding driving and operating machinery, hypersensitivity reactions, may reduce effectiveness of oral contraceptives, use in pregnant or breast-feeding women and dose selection in geriatric patients.

Conditions of clinical use, adverse reactions, drug interactions and dosing instructions.

 

FOR MORE INFORMATION

For any questions related to UBRELVY, you can contact AbbVie Medical Information at 1-844-241-5011

SAFETY INFORMATION

Click here for additional safety information and for a link to the Product Monograph discussing:

Contraindications with concomitant use of strong CYP3A4 inhibitors.

Relevant warnings and precautions regarding driving and operating machinery, hypersensitivity reactions, may reduce effectiveness of oral contraceptives, use in pregnant or breast-feeding women and dose selection in geriatric patients.

Conditions of clinical use, adverse reactions, drug interactions and dosing instructions.

 

FOR MORE INFORMATION

For any questions related to UBRELVY, you can contact AbbVie Medical Information at
1-844-241-5011

Pain relief was defined as a change in the severity of headache pain from moderate or severe pain to mild pain or no pain at 2 hours after the initial dose.

Modified intent-to-treat (mITT) population included all randomized patients who received at least 1 dose of investigational product, recorded a baseline migraine headache severity measurement, and had ≥1 post-dose migraine headache severity measurement at or before the 2-hour timepoint.

§Freedom from pain was defined as a change in the severity of headache pain from moderate or severe pain to the presence of no pain at 2 hours after the initial dose.

References:

1. UBRELVY (ubrogepant) Product Monograph. AbbVie Corporation. 

2. Dodick W, et al. Ubrogepant for the Treatment of Migraine. N Engl J Med 2019;381:2230-2241.

UBRELVY and its design are trademarks of Allergan Pharmaceuticals International Limited, an AbbVie company, used under license by AbbVie Corporation. 

© 2024 AbbVie. All rights reserved. 

CA-UBR-230004A / JN24  

UBRELVY and its design are trademarks of Allergan Pharmaceuticals International Limited, an AbbVie company, used under license by AbbVie Corporation. 

© 2024 AbbVie. All rights reserved. 

CA-UBR-230004A / JN24  

ABOUT THIS STUDY1

ACHIEVE I was a randomized, double-blind, placebo-controlled, single migraine attack study. Patients were randomized to UBRELVY 50 mg (n=423) or 100 mg (n=448) or placebo (n=456).

This study enrolled patients with a history of migraine with and without aura who experienced 2 to 8 migraine attacks per month with moderate to severe headache pain.

Patients were permitted to use standard migraine preventive medications during the study.

Patients were instructed to treat a migraine with moderate to severe headache pain intensity within the first 4 hours of pain onset.

An optional second dose of medication or the patient’s usual acute treatment for migraine was allowed 2 to 48 hours after the initial treatment for a non-responding or recurrent migraine headache. Results shown reflect response after the single initial dose only.

 

Reference:

1. UBRELVY (ubrogepant) Product Monograph. AbbVie Corporation. 

ABOUT THIS STUDY1

ACHIEVE I was a randomized, double-blind, placebo-controlled, single migraine attack study. Patients were randomized to UBRELVY 50 mg (n=423) or 100 mg (n=448) or placebo (n=456).

This study enrolled patients with a history of migraine with and without aura who experienced 2 to 8 migraine attacks per month with moderate to severe headache pain.

Patients were permitted to use standard migraine preventive medications during the study.

Patients were instructed to treat a migraine with moderate to severe headache pain intensity within the first 4 hours of pain onset.

An optional second dose of medication or the patient’s usual acute treatment for migraine was allowed 2 to 48 hours after the initial treatment for a non-responding or recurrent migraine headache. Results shown reflect response after the single initial dose only.

 

Reference:

1. UBRELVY (ubrogepant) Product Monograph. AbbVie Corporation.