drugset / Trial / NCT02790034

Evaluation of the Efficacy, Safety, and Tolerability of Sarizotan in Rett Syndrome With Respiratory Symptoms

NCT02790034 ↗

Phase 2/3 Terminated 129 enrolled Newron Pharmaceuticals SPA
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study evaluates the safety, tolerability and efficacy of Sarizotan in reducing respiratory abnormalities in Rett Syndrome in an initial double blind 24 week period followed by an open label treatment phase of up to 168 weeks (the latter for patients with no safety and tolerability issues).

Timeline

Start
2016-10-26
Primary completion
2019-08-06
Completion
2020-05-04

Outcome

Missed primary endpoint

Stopped: “The study did not demonstrate evidence of efficacy on the primary or secondary efficacy variables”

registry analysis (superiority test); Sarizotan High Dose vs Placebo; p = 0.6411; Mean Difference (Final Values) -5.292 (95% CI -27.741 to 17.157); Mixed Models Analysis NCT02790034 ↗

registry analysis (superiority test); Sarizotan Low Dose vs Placebo; p = 0.2011; Mean Difference (Final Values) -16.966 (95% CI -43.119 to 9.186); Mixed Models Analysis NCT02790034 ↗

release “STARS clinical study evaluating sarizotan in patients with Rett syndrome did not demonstrate evidence of efficacy on the primary or secondary efficacy variables.” newron.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Sarizotan Small molecule 2 mg —
Subject Sarizotan Small molecule 5 mg —
Subject Sarizotan Small molecule 10 mg —

Indications