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Johnson & Johnson submits sNDA to US FDA for Caplyta for prevention of relapse in schizophrenia: Titusville, New Jersey Wednesday, July 9, 2025, 14:00 Hrs [IST] Johnson & Johnson ...
Titusville: Johnson & Johnson has submitted a supplemental New Drug Application (sNDA) to the U.S. Food and Drug ...
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MedPage Today on MSNAntidepressant Discontinuation Symptoms; Medicaid 1115 Waiver Review? RSD ExplainedA 49-study meta-analysis showed that the mean number of discontinuation symptoms 1 week after stopping an antidepressant was ...
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Johnson & Johnson Submits Supplemental Drug Application To FDA For Schizophrenia Drug CaplytaJohnson & Johnson (JNJ) said on Tuesday that it has submitted a supplemental new drug application to the U.S. Food and Drug ...
Johnson & Johnson (NYSE:JNJ) submitted a supplemental New Drug Application for CAPLYTA®, aiming to prevent schizophrenia ...
The supplemental New Drug Application is supported by Phase III data, which showed Caplyta significantly prolonged time to ...
Welcome to Fierce Pharma's regulatory tracker for the second half of 2025. | In this tracker, Fierce Pharma is recording the ...
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Optum Rx officials said they now have eliminated reauthorization requirements for more than 140 chronic disease medications.
What is Schizophrenia?Schizophrenia is a chronic and often debilitating mental disorder, is characterized by symptoms such as ...
Caplyta may cause serious side effects, but these are not common. The following list may not include all possible serious side effects of the drug. For more information, you can refer to Caplyta ...
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