TY - JOUR
T1 - Oral ENT-01 Targets Enteric Neurons to Treat Constipation in Parkinson Disease A Randomized Controlled Trial
AU - Camilleri, Michael
AU - Subramanian, Thyagarajan
AU - Pagan, Fernando
AU - Isaacson, Stuart
AU - Gil, Ramon
AU - Hauser, Robert A.
AU - Feldman, Mary
AU - Goldstein, Mark
AU - Kumar, Rajeev
AU - Truong, Daniel
AU - Chhabria, Nisha
AU - Walter, Benjamin L.
AU - Eskenazi, Jonathan
AU - Riesenberg, Robert
AU - Burdick, Daniel
AU - Tse, Winona
AU - Molho, Eric
AU - Robottom, Bradley
AU - Bhatia, Perminder
AU - Kadimi, Srinath
AU - Klos, Kevin
AU - Shprecher, David
AU - Marquez-Mendoza, Otto
AU - Hidalgo, Gonzalo
AU - Grill, Stephen
AU - Li, George
AU - Mandell, Howard
AU - Hughes, Mary
AU - Stephenson, Sharisse
AU - Vandersluis, Joel
AU - Pfeffer, Michael
AU - Duker, Andrew
AU - Shivkumar, Vikram
AU - Kinney, William
AU - MacDougall, James
AU - Zasloff, Michael
AU - Barbut, Denise
N1 - Publisher Copyright:
© 2022 American College of Physicians. All rights reserved.
PY - 2022/12
Y1 - 2022/12
N2 - Background: Parkinson disease (PD) is associated with a-synuclein (aS) aggregation within enteric neurons. ENT-01 inhibits the formation of aS aggregates and improved constipation in an open-label study in patients with PD. Objective: To evaluate the safety and efficacy of oral ENT-01 for constipation and neurologic symptoms in patients with PD and constipation. Design: Randomized, placebo-controlled phase 2b study. (ClinicalTrials.gov: NCT03781791) Setting: Outpatient. Patients: 150 patients with PD and constipation. Intervention: 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. Measurements: 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]). Results: 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). Limitation: Longer treatment periods need to be investigated in future studies. Conclusion: ENT-01 was safe and significantly improved constipation.
AB - Background: Parkinson disease (PD) is associated with a-synuclein (aS) aggregation within enteric neurons. ENT-01 inhibits the formation of aS aggregates and improved constipation in an open-label study in patients with PD. Objective: To evaluate the safety and efficacy of oral ENT-01 for constipation and neurologic symptoms in patients with PD and constipation. Design: Randomized, placebo-controlled phase 2b study. (ClinicalTrials.gov: NCT03781791) Setting: Outpatient. Patients: 150 patients with PD and constipation. Intervention: 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. Measurements: 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]). Results: 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). Limitation: Longer treatment periods need to be investigated in future studies. Conclusion: ENT-01 was safe and significantly improved constipation.
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U2 - 10.7326/M22-1438
DO - 10.7326/M22-1438
M3 - Article
C2 - 36343348
AN - SCOPUS:85144589441
SN - 0003-4819
VL - 175
SP - 1666
EP - 1675
JO - Annals of Internal Medicine
JF - Annals of Internal Medicine
IS - 12
ER -