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Oral ENT-01 Targets Enteric Neurons to Treat Constipation in Parkinson Disease

医学 便秘 耐受性 安慰剂 内科学 泻药 胃肠病学 临床终点 排便 随机对照试验 不利影响 病理 替代医学
作者
Michael Camilleri,Thyagarajan Subramanian,Fernando Pagán,Stuart Isaacson,Ramon Gil,Robert A. Hauser,Mary Feldman,Larry B. Goldstein,Rajeev Kumar,Daniel Truong,Nisha Chhabria,Benjamin L. Walter,Jonathan Eskenazi,Robert Riesenberg,Daniel Burdick,Winona Tse,Eric Molho,B. Robottom,Perminder Bhatia,Srinath Kadimi,Kevin J. Klos,David Shprecher,Otto Marquez-Mendoza,Gonzalo Hidalgo,Stephen Grill,George Li,Howard Mandell,Mary Hughes,Sharisse Stephenson,Joel Vandersluis,Michael A. Pfeffer,Andrew P. Duker,Vikram Shivkumar,William A. Kinney,James E. MacDougall,Michael Zasloff,Denise Barbut
出处
期刊:Annals of Internal Medicine [American College of Physicians]
卷期号:175 (12): 1666-1674 被引量:27
标识
DOI:10.7326/m22-1438
摘要

Parkinson disease (PD) is associated with α-synuclein (αS) aggregation within enteric neurons. ENT-01 inhibits the formation of αS aggregates and improved constipation in an open-label study in patients with PD.To evaluate the safety and efficacy of oral ENT-01 for constipation and neurologic symptoms in patients with PD and constipation.Randomized, placebo-controlled phase 2b study. (ClinicalTrials.gov: NCT03781791).Outpatient.150 patients with PD and constipation.ENT-01 or placebo daily for up to 25 days. After baseline assessment of constipation severity, daily dosing was escalated to the prokinetic dose, the maximum dose (250 mg), or the tolerability limit, followed by a washout period.The primary efficacy end point was the number of complete spontaneous bowel movements (CSBMs) per week. Neurologic end points included dementia (assessed using the Mini-Mental State Examination [MMSE]) and psychosis (assessed using the Scale for the Assessment of Positive Symptoms adapted for PD [SAPS-PD]).The weekly CSBM rate increased from 0.7 to 3.2 in the ENT-01 group versus 0.7 to 1.2 in the placebo group (P < 0.001). Improvement in secondary end points included SBMs (P = 0.002), stool consistency (P < 0.001), ease of passage (P = 0.006), and laxative use (P = 0.041). In patients with dementia, MMSE scores improved by 3.4 points 6 weeks after treatment in the ENT-01 group (n = 14) versus 2.0 points in the placebo group (n = 14). Among patients with psychosis, SAPS-PD scores improved from 6.5 to 1.7 six weeks after treatment in the ENT-01 group (n = 5) and from 6.3 to 4.4 in the placebo group (n = 6). ENT-01 was well tolerated, with no deaths or drug-related serious adverse events. Adverse events were predominantly gastrointestinal, including nausea (34.4% [ENT-01] vs. 5.3% [placebo]; P < 0.001) and diarrhea (19.4% [ENT-01] vs. 5.3% [placebo]; P = 0.016).Longer treatment periods need to be investigated in future studies.ENT-01 was safe and significantly improved constipation.Enterin, Inc.
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