J&J's paliperidone LA shows 13-week control

22 December 2008

Johnson & Johnson's investigational long-acting schizophrenia drug paliperidone palmitate demonstrated statistically-significant symptom control compared with placebo, according to the results of a 13-week study.

The US health care major says that statistical significance was seen at all doses of the antipsychotic tested (25mg, 100mg, and 150mg equivalent), when given every four weeks with a 150mg initiation dose.

The agent is a long-acting formulation of the oral drug Invega (paliperidone extended-release), which is approved for the acute and maintenance treatment of schizophrenia. Because of the delivery systems used, LA formulations may produce more consistent levels of the drug, J&J noted.

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