Levodopa formulations for rapid relief of parkinson's disease
A levodopa, Parkinson's disease technology, applied in the field of levodopa preparations for rapid relief of Parkinson's disease, capable of solving problems such as poor intestinal uptake
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Embodiment 1
[0095] overview
[0096] The 90 / 8 / 2 dry powder levodopa formulation is provided to evaluate the safety, tolerability, and Dopa Pharmacokinetics (PK). The pulmonary levodopa powder described in these examples consisted of 90% levodopa granules, 8% dipalmitoylphosphatidylcholine, and 2% sodium chloride (all on a dry basis) and is referred to herein as "90 / 8 / 2". This data provides an indication of the PK of levodopa following a single inhaled dose of 90 / 8 / 2, compared to oral levodopa (LD) administered under fasted and fed conditions, and with and without carbidol. Comparison of PK in the case of bar (CD) pretreatment. This was a two-part study in healthy adult male and female subjects, as follows: Part A - dose escalation segment compared to oral levodopa; and Part B - 90 / 8 / 2 plus or minus carb Dopa pretreatment link.
[0097] Part A is an open-label, 3-period crossover, single dose escalation study. Each subject received a single oral dose of CD / LD (25 / 100 mg) in the fed...
Embodiment 2
[0189] A phase 2 study testing two doses of pulmonary levodopa (25 mg and 50 mg of study drug) was a multicentre, randomized, double-blind, placebo-controlled, single-dose, with three arms (placebo, 25 mg, and 50 mg ) and included an "open-label" oral Sinemet arm. Twenty-four (24) patients treated in this study were serially assessed for L-dopa plasma levels, exercise response, and safety at each visit. Study drug was administered to patients in the off state and serial assessments began prior to dosing and continued for up to 180 minutes after dosing. Motor function was assessed using the tap test, the Unified Parkinson's Disease Rating Scale Part III (UPDRS III), and subjective assessments of "meaningful" on and off. Safety parameters monitored included pulmonary function, clinical laboratory data, EGC, and vital signs (blood pressure, heart rate, and orthostatic blood pressure). This study was designed to measure the timing, magnitude, and persistence of pulmonary levodop...
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