An Open-Label, Long-Term Safety, Tolerability, and Efficacy Study of TEV-50717 (Deutetrabenazine) for the Treatment of Dyskinesia in Cerebral Palsy in Children and Adolescents (Open RECLAIM-DCP)

  • STATUS
    Recruiting
  • participants needed
    185
  • sponsor
    Teva Branded Pharmaceutical Products R&D, Inc.
Updated on 22 September 2023

Summary

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.

Details
Condition Cerebral Palsy, Dyskinetic
Treatment TEV-50717
Clinical Study IdentifierNCT04200352
SponsorTeva Branded Pharmaceutical Products R&D, Inc.
Last Modified on22 September 2023

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