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Atogepant

Generic Name
Atogepant
Brand Names
Qulipta, Aquipta
Drug Type
Small Molecule
Chemical Formula
C29H23F6N5O3
CAS Number
1374248-81-3
Unique Ingredient Identifier
7CRV8RR151

Overview

Atogepant is an oral antagonist of calcitonin gene-related peptide (CGRP) receptors indicated for the prevention of episodic migraine headaches. It was developed by AbbVie and received FDA approval under the brand name Qulipta in September 2021. While its approval was predated by two other members of the same drug family, namely ubrogepant and rimegepant, these agents are indicated only for abortive migraine therapy - atogepant is novel in that it is the first and only oral CGRP antagonist approved for preventative use in migraine. In December 2022, atogepant received Health Canada approval for the prevention of episodic migraine in adults. It also received approval for preventive treatment of adult migraine by the EMA in August 2023. In patients requiring preventative migraine therapy, current practice guidelines recommend the use of certain anti-epileptic medications (e.g. valproic acid or topiramate) or beta-blockers (e.g. propranolol), all of which can be associated with significant adverse effects. The "gepants" family of drugs, including atogepant, are comparatively well-tolerated and may provide a desirable treatment option for patients struggling with adverse reactions to other preventative therapies.

Background

Atogepant is an oral antagonist of calcitonin gene-related peptide (CGRP) receptors indicated for the prevention of episodic migraine headaches. It was developed by AbbVie and received FDA approval under the brand name Qulipta in September 2021. While its approval was predated by two other members of the same drug family, namely ubrogepant and rimegepant, these agents are indicated only for abortive migraine therapy - atogepant is novel in that it is the first and only oral CGRP antagonist approved for preventative use in migraine. In December 2022, atogepant received Health Canada approval for the prevention of episodic migraine in adults. It also received approval for preventive treatment of adult migraine by the EMA in August 2023. In patients requiring preventative migraine therapy, current practice guidelines recommend the use of certain anti-epileptic medications (e.g. valproic acid or topiramate) or beta-blockers (e.g. propranolol), all of which can be associated with significant adverse effects. The "gepants" family of drugs, including atogepant, are comparatively well-tolerated and may provide a desirable treatment option for patients struggling with adverse reactions to other preventative therapies.

Indication

Atogepant is indicated for the preventive treatment of migraine in adults by the FDA, EMA, and Health Canada.

Associated Conditions

  • Episodic Migraine
  • Migraine

FDA Approved Products

Qulipta
Manufacturer:AbbVie Inc.
Route:ORAL
Strength:60 mg in 1 1
Approved: 2024/02/09
NDC:0074-7094
Qulipta
Manufacturer:AbbVie Inc.
Route:ORAL
Strength:30 mg in 1 1
Approved: 2024/02/09
NDC:0074-7096
Qulipta
Manufacturer:AbbVie Inc.
Route:ORAL
Strength:10 mg in 1 1
Approved: 2024/02/09
NDC:0074-7095

Singapore Approved Products

AQUIPTA TABLET 10MG
Manufacturer:Forest Laboratories Ireland, Limited
Form:TABLET
Strength:10.0mg
Online:Yes
Approved: 2024/11/29
Approval:SIN17145P
AQUIPTA TABLET 60MG
Manufacturer:Forest Laboratories Ireland, Limited
Form:TABLET
Strength:60.0mg
Online:Yes
Approved: 2024/11/29
Approval:SIN17146P

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