Atogepant (Qulipta)
Small-molecule CGRP receptor antagonist approved for episodic and chronic migraine prevention; 10 mg, 30 mg, or 60 mg once daily. Plasma half-life ~11h. Unlike rimegepant is not dosed acutely. Metabolized by CYP3A4; dose-reduce with strong inhibitors.
Projected serum levels — 60 mg, once daily
Maintenance schedule: 60 mg once daily (oral).
Loading schedule: 74.7 mg on day 1, then 60 mg once daily — reaching therapeutic levels sooner.
Modeled steady state after ~2 days: peak ≈ 14.7 mg, trough ≈ 3.4 mg body load. Population-based estimate over 15 days for a 60 mg dose at a 70 kg reference body mass — the interactive app scales curves to your doses, timing, and body mass.
Key facts
- Category
- CGRP Antagonist
- Route modeled
- Oral
- Model confidence
- inferred
- Half-life
- 11 h
- Common dose
- 60 mg
- Suggested maximum
- 60 mg/day
- Reference dose range
- 30–60 mg (single dose)
- Suggested cadence
- once daily
- Validated against
- 60 mg oral — Cmax 0.20 mg/L at 2 h
Documented interactions
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contraindicated
Carbamazepine (Tegretol) + Atogepant (Qulipta)
Carbamazepine (Tegretol) inducer of CYP3A4 predicted to change Atogepant (Qulipta) AUC by ~0.20x
-
contraindicated
Clarithromycin (Biaxin) + Atogepant (Qulipta)
Clarithromycin (Biaxin) mechanism_based of CYP3A4 predicted to change Atogepant (Qulipta) AUC by ~10.00x
-
contraindicated
Dasatinib (Sprycel) + Atogepant (Qulipta)
Dasatinib (Sprycel) time_dependent_inhibitor of CYP3A4 predicted to change Atogepant (Qulipta) AUC by ~5.00x
-
contraindicated
Diltiazem + Atogepant (Qulipta)
Diltiazem mechanism_based of CYP3A4 predicted to change Atogepant (Qulipta) AUC by ~10.00x
-
contraindicated
Efavirenz (Sustiva) + Atogepant (Qulipta)
Efavirenz (Sustiva) inducer of CYP3A4 predicted to change Atogepant (Qulipta) AUC by ~0.12x
-
contraindicated
Grapefruit (whole fruit) + Atogepant (Qulipta)
Grapefruit (whole fruit) mechanism_based of CYP3A4 predicted to change Atogepant (Qulipta) AUC by ~10.00x
Serum checks 94 modeled interaction pairings for atogepant (qulipta) across your whole stack — absorption conflicts, enzyme inhibition, and nutrient depletion included.
Research behind this entry
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Single-dose pharmacokinetics and safety of atogepant in participants with hepatic impairment
PK study in hepatic impairment informing dose recommendations and characterizing atogepant's ~11h half-life.
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Atogepant for the preventive treatment of migraine (ADVANCE)
ADVANCE phase 3 trial demonstrating atogepant 10/30/60 mg daily significantly reduced monthly migraine days in episodic migraine prevention.
2 published studies referenced in the app, each with a plain-language summary.