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Medicure Pharma is currently evaluating the safety and efficacy of TARDOXAL® to treat patients with tardive dyskinesia.
Tardive dyskinesia is a serious movement disorder resulting from long-term treatment with antipsychotic medications. Tardive dyskinesia is characterized by repetitive, involuntary, purposeless movements, and can also be accompanied by psychotic symptoms of depression, and feelings of anger and embarrassment. Tardive dyskinesia is associated with poor quality of life and increased medical morbidity and mortality, however the mechanisms involved in the pathogenesis of tardive dyskinesia are poorly understood.
Medicure has filed an FDA IND and conducted a 12-week, randomized, double-blind, placebo-controlled, parallel group comparative study to evaluate the safety and efficacy of TARDOXAL in the treatment of tardive dyskinesia in patients with schizophrenia and schizoaffective disorders. Medicure is evaluating further clinical studies to pursue.
Reuben Saba, PhD
VP, Medical and Business Affairs
Email: rsaba@medicure.com
Recent NewsMedicure Announces Pivotal Phase 3 Trial IND Filing with FDA for Treatment of Seizures Associated with Pyridox(am)ine 5'-phosphate oxidase (PNPO) Deficiency |
Clinical Trials: MC-1Medicure is conducting the MEND-PNPO study, a Phase 3 study to assess the safety and efficacy of MC-1 in patients with confirmed PNPO deficiency via genetic analysis. |
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