Amneal Announces Positive Interim Phase 4 ELEVATE-PD Results With CREXONT® for Parkinson's Disease

Core Insights - Amneal Pharmaceuticals announced positive interim results from its Phase 4 ELEVATE-PD study for CREXONT, a new treatment for Parkinson's disease, showcasing significant clinical benefits for patients [1][2]. Group 1: Study Results - The first 55 patients in the study showed substantial improvements after six weeks of treatment with CREXONT, including an increase in daily "Good On" time by 1.86 hours, a reduction in "Off" time by 0.77 hours, and an increase in "Good On" time per dose by 0.79 hours [3][4]. - The MDS-UPDRS total score improved by an average of -14.2 points, indicating enhanced motor function [4]. - CREXONT demonstrated a longer duration of benefit with each dose compared to other oral carbidopa/levodopa therapies, highlighting its differentiated clinical performance [4][5]. Group 2: Safety and Efficacy - Treatment-emergent adverse events (TEAEs) were generally mild to moderate, with common side effects including nausea (5.5%), falls (3.6%), dizziness (3.6%), and urinary tract infection (3.6%) [6]. - The ongoing ELEVATE-PD study aims to provide longer-term data and patient-reported outcomes in 2026, further supporting CREXONT's impact on motor symptom control and functional independence [6][8]. Group 3: Product Information - CREXONT is an innovative formulation that combines immediate-release granules and extended-release pellets, designed to optimize levodopa delivery and absorption, providing the longest-lasting plasma levels of any oral CD/LD therapy available [2][7]. - The ELEVATE-PD study is an open-label, multi-center clinical trial designed to evaluate the real-world efficacy and safety of switching to CREXONT in adults with moderately severe Parkinson's disease [8].