Janssen-Cilag International NV announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA)...
Janssen-Cilag International NV announced that the European Commission (EC) has approved the use of Trevicta (paliperidone palmitate a three monthly...
The FDA has approved Luye Pharma’s paliperidone palmitate (Erzofri) extended-release injectable suspension for the treatment of schizophrenia in adults and schizoaffective disorder in adults as monotherapy, as well as an adjunct to mood stabilizers or antidepressants
A study published in The Journal of Clinical Psychiatry shows that long-acting Invega Sustenna (paliperidone palmitate), from Janssen Pharmaceuticals, was...
Janssen Research & Development, LLC (Janssen) has announced the submission of a New Drug Application (NDA) for three-month atypical antipsychotic...
The FDA approved the supplemental New Drug Applications (sNDAs) for the once-monthly atypical long-acting antipsychotic Invega Sustenna (paliperidone palmitate), from...
The Janssen Pharmaceutical Companies of Johnson & Johnson has announced the FDA has approved long-acting atypical antipsychotic Invega Hafyera (6-month paliperidone palmitate), the first-and-only twice-yearly injectable for the treatment of schizophrenia in adults.
Three-month treatment with Invega Sustenna/Xeplion (paliperidone palmitate), from Janssen Pharmaceuticals, significantly delayed time to relapse compared to placebo in patients...
Janssen Pharmaceuticals, Inc. announced that the FDA approved under priority review the New Drug Application (NDA) for the three-month long-acting...
Janssen Pharmaceuticals has announced results of its landmark PRIDE trial, a prospective, randomized clinical trial to compare Invega Sustenna/Xeplion (paliperidone...