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Teva's new monthly schizophrenia injection showed no serious side effects in a large trial and may improve patient adherence.
Teva Pharmaceuticals reported no cases of post-injection delirium/sedation syndrome in the Phase 3 SOLARIS trial for its once-monthly olanzapine LAI (TEV-749) over 56 weeks in over 675 adults with schizophrenia.
The long-acting injectable, using SteadyTeq™ technology, showed a safety profile consistent with other second-generation antipsychotics.
Separate data suggested UZEDY (risperidone) was linked to shorter hospital stays than Invega Sustenna in hospitalized patients, though no direct comparisons were made.
Teva highlighted the potential of olanzapine LAI to improve treatment adherence and outcomes for schizophrenia patients struggling with daily pills.
La nueva inyección mensual contra la esquizofrenia de Teva no mostró efectos secundarios graves en un ensayo de gran tamaño y puede mejorar la adherencia del paciente.