This website contains information about
INBRIJA® (levodopa inhalation powder)
M-INB-UK-0047
Date of preparation: December 2025
This website is intended for healthcare professionals from the United Kingdom only. Adverse event reporting information can be found at the bottom of the page.
Rapid
Observed relief in as
little as 10 minutes2,3
RELIABLE
Pulmonary route avoids
variability caused by GI
tract absorption4
ON-DEMAND
Supporting patients when
needed, up to 5 times per day4
*The least squares mean difference between the 84 mg dose and placebo was –3.92 (–6.84 to –1.00) as measured by UPDRS motor score from pre dose to 30 minutes post dose.
In a 12-week, randomised, double-blind, placebo-controlled phase III trial of INBRIJA®, adults with Parkinson’s disease experiencing at least 2 hours of daily OFF time despite stable oral levodopa therapy were enrolled. Participants were randomised (1:1:1) to INBRIJA® 60 mg, 84† mg, or placebo, administered as needed for OFF episodes (up to five times daily) in addition to their standard regimen. The primary endpoint was the change in Unified Parkinson’s disease rating scale (UPDRS) Part III motor score from pre-dose to 30 minutes post-dose at week 12 during an in-clinic OFF period.2
GI; Gastrointestinal; UPDRS, Unified Parkinson’s Disease Rating Scale.
†The recommended dose of INBRIJA® is 2 hard capsules each containing 42 mg levodopa. Each delivered dose per capsule contains 33 mg levodopa.
M-INB-UK-0047
Date of preparation: December 2025