Eptinezumab (Vyepti)
Humanized IgG1 monoclonal antibody targeting CGRP ligand, administered IV every three months for migraine prevention (100 mg or 300 mg IV q12 weeks). IV administration yields 100% bioavailability and rapid onset (within day 1 post-infusion). Biphasic PK with terminal half-life ~27 days. Well tolerated; nasopharyngitis and rare hypersensitivity reactions reported. Requires infusion center visit - borderline at-home vs clinic-administered tracking.
Projected serum levels — 100 mg, custom (shown daily)
Maintenance schedule: 100 mg custom (shown daily) (iv).
Loading schedule: 300 mg on day 1, then 100 mg custom (shown daily) — reaching therapeutic levels sooner.
Modeled steady state after ~73 days: peak ≈ 3.7k mg, trough ≈ 3.7k mg body load. Population-based estimate over 121 days for a 100 mg dose at a 70 kg reference body mass — the interactive app scales curves to your doses, timing, and body mass.
Key facts
- Category
- Biologic
- Route modeled
- IV
- Model confidence
- inferred
- Half-life
- 27 days
- Common dose
- 100 mg
- Suggested maximum
- 300 mg/day
- Reference dose range
- 50–300 mg (single dose)
- Suggested cadence
- custom (shown daily)
- Validated against
- 100 mg iv — Cmax 27 mg/L at 0.25 h
Documented interactions
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Atogepant (Qulipta) + Eptinezumab (Vyepti)
Atogepant (Qulipta) and Eptinezumab (Vyepti) both push the cgrp receptor in the same direction.
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Erenumab (Aimovig) + Eptinezumab (Vyepti)
Eptinezumab (Vyepti) and Erenumab (Aimovig) both push the cgrp receptor in the same direction.
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Rimegepant (Nurtec ODT) + Eptinezumab (Vyepti)
Eptinezumab (Vyepti) and Rimegepant (Nurtec ODT) both push the cgrp receptor in the same direction.
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Ubrogepant (Ubrelvy) + Eptinezumab (Vyepti)
Eptinezumab (Vyepti) and Ubrogepant (Ubrelvy) both push the cgrp receptor in the same direction.
Serum checks 4 modeled interaction pairings for eptinezumab (vyepti) across your whole stack — absorption conflicts, enzyme inhibition, and nutrient depletion included.
Research behind this entry
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Pharmacokinetics, safety, and tolerability of eptinezumab in patients with migraine
Clinical PK analysis establishing eptinezumab's ~27-day terminal half-life, IV bioavailability, and exposure-response relationship.
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Eptinezumab in episodic migraine: A randomized, double-blind, placebo-controlled study (PROMISE-1)
PROMISE-1 phase 3 trial demonstrating quarterly IV eptinezumab reduces monthly migraine days in episodic migraine.
2 published studies referenced in the app, each with a plain-language summary.