drugset / Trial / NCT05475483

Efficacy and Safety on SOM3355 in Huntington's Disease Chorea

NCT05475483 ↗

Phase 2 Completed 139 enrolled SOM Innovation Biotech SA
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Phase IIb, randomized, double-blind, placebo-controlled study in parallel groups assessing the efficacy and safety of two doses of SOM3355 in patients suffering from Huntington's Disease with choreic movements.

Timeline

Start
2022-08-02
Primary completion
2024-06-25
Completion
2024-07-15

Outcome

Met primary endpoint

registry analysis (other test); Placebo vs SOM3355 600 mg/Day; p = 0.045; Mean Difference (Final Values) -1.27 (95% CI -2.51 to -0.03); Mixed Models Analysis NCT05475483 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject BEVANTOLOL Small molecule 200 mg —
Subject BEVANTOLOL Small molecule 300 mg —

Indications