Section 03 · Monograph

Tavapadon

Reviewed Nov 2026FDA label
JuvmoD1/D5 dopamine partial agonist
Forms
Tab: 5, 10, 15mg | Titration pack: 0.25, 1mg tabs
Dose
Once daily with or without levodopa (monotherapy in early PD or adjunct for motor fluctuations); ~6-week titration to maintenance dose; no label contraindications
MOA
Selective D1/D5 receptor partial agonism (CYP3A substrate)

Indications

  • Parkinson's disease in adults: monotherapy in early disease and adjunct to levodopa in patients with motor fluctuations (FDA-approved September 2026)FDA-labeled

Mechanism of Action

  • Selective D1/D5 dopamine receptor partial agonist, distinct from D2/D3-targeting dopamine agonists

Full Dosing

Adult / usual

  • Once-daily oral tablets (5, 10, 15mg) with a titration pack of 0.25mg and 1mg tablets; label titration takes about 6 weeks

Renal

  • This is a newly approved product — confirm the exact titration schedule, hepatic/renal adjustments and CYP3A interaction dosing in the current prescribing information

Contraindications

  • None listed in labeling

Drug Interactions

  • CYP3A substrate: strong CYP3A inhibitors or inducers affect exposure — see label
  • Dopamine antagonists may reduce effectiveness

Adverse Effects

  • Dopaminergic class effects per label (for example somnolence and sudden sleep onset, nausea, dizziness, hallucinations and impulse-control behaviors) — verify against the current prescribing information
  • Patients older than 80 years were excluded from pivotal trials

Monitoring Parameters

  • Daytime sleepiness, orthostatic blood pressure, psychiatric and impulse-control symptoms
  • Motor fluctuations and levodopa dose

Pregnancy & Lactation

  • Limited data; confirm in current prescribing information

References

  1. JUVMO (tavapadon) Prescribing Information — AbbVie