Study TV50717-CNS-30081 is a 55-week study in which patients who have successfully completed the parent study (Study TV50717-CNS-30080) may be eligible to enroll in this study.
The primary objective of this study is to evaluate the safety and tolerability of long-term therapy with TEV-50717 in children and adolescents with DCP.
The secondary objective of this study is to evaluate the efficacy of long-term therapy with TEV-50717 in reducing the severity of DCP.
Condition | Cerebral Palsy, Dyskinetic |
---|---|
Treatment | TEV-50717 |
Clinical Study Identifier | NCT04200352 |
Sponsor | Teva Branded Pharmaceutical Products R&D, Inc. |
Last Modified on | 22 September 2023 |
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