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Efficacy and safety of ecopipam for Tourette syndrome: An updated systematic review and meta-analysis of randomized controlled trials

Journal
Therapeutic advances in psychopharmacology (Q1)
Published
2 September 2026
Study design
Systematic review / meta-analysis of RCTs
Evidence level
Level 1, High (CEBM 1a)
Authors
Aasim Ali, Abdullah Shahid, Muhammad Usman, Asad Ullah Ansari, Labeeba Abdul Ghafoor, Csilla Dézsi, et al.
PMID
42694316
DOI
10.1177/20451253261487299

Why clinicians should know about it

  • Picked for Pharmacology (medical) (top studies of the week, 6 September 2026): Ecopipam efficacy and safety for Tourette syndrome (RCTs)

Abstract

BACKGROUND: Tourette syndrome is a neurodevelopmental disorder characterized by persistent motor and vocal tics. Dopamine D2 receptor antagonists can reduce tic severity but are frequently limited by metabolic, sedative, and extrapyramidal adverse effects. Ecopipam is a selective dopamine D1/D5 receptor antagonist with a potentially distinct tolerability profile. OBJECTIVES: To evaluate the efficacy and safety of ecopipam in patients with Tourette syndrome using updated randomized evidence. DESIGN: Systematic review and random-effects meta-analysis of randomized placebo-controlled trials. DATA SOURCES AND METHODS: PubMed/MEDLINE, Embase, Scopus, ClinicalTrials.gov, reference lists, and conference sources were searched from database inception to May 31, 2026. The primary outcome was change in Yale Global Tic Severity Scale Total Tic Score. Headache and insomnia were evaluated as safety outcomes. Treatment estimates were pooled using random-effects models with Hartung-Knapp adjustment. Risk of bias was assessed using the Cochrane RoB 2 tool. RESULTS: Three randomized trials involving 297 unique randomized participants were included. Ecopipam improved tic severity compared with placebo (mean difference, -3.72; 95% confidence interval, -5.96 to -1.47). The result remained significant after exclusion of the phase 3 randomized-withdrawal trial (mean difference, -3.33; 95% confidence interval, -4.85 to -1.81). No statistical heterogeneity was detected for efficacy outcomes, although the small number of trials limits interpretation. Headache was not significantly increased (risk ratio, 1.36; 95% confidence interval, 0.52-3.51). Insomnia showed an imprecise, nonsignificant association (risk ratio, 2.44; 95% confidence interval, 0.07-79.93; I2=62.2%). CONCLUSION: Short-term randomized evidence suggests that ecopipam reduces tic severity. Evidence concerning insomnia and long-term psychiatric and metabolic safety remains insufficient, requiring larger independent trials with longer follow-up.

Abstract as published, via PubMed.

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For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.