Unfortunately, an FDA policy — specifically the Risk Evaluation and Mitigation Strategies (REMS) program — has been largely ...

The U.S. Food and Drug Administration has approved Bristol Myers Squibb's Cobenfy (xanomeline and trospium chloride), a first ...

Revuforj is the first so-called menin inhibitor cleared in the U.S., securing FDA approval for use in adults and certain ...

"Severe neutropenia occurs in a small percentage of patients taking clozapine; however, neutropenia is associated with an ...

An inspection of a Tom's of Maine manufacturing facility found that the brand's toothpaste was produced with water containing ...

With the failure of AbbVie’s emraclidine in two mid-stage trials, Bristol Myers Squibb’s Cobenfy is 'sole muscarinic winner.' ...

The shocking failure of AbbVie’s emraclidine has investors questioning the Big Pharma’s long-term neuroscience strategy, ...

An unnecessary FDA policy is making it nearly impossible for schizophrenics without stable medical care to get clozapine, the only medicine useful for treatment-resistant schizophrenia. In the absence ...

the only FDA-approved drug for treatment-resistant schizophrenia, the most severe form of the disorder. The FDA established REMS in 2007 to ensure safety precautions for certain drugs with ...

The FDA approved clozapine, which is classified as an “atypical” antipsychotic drug, for treatment-resistant schizophrenia in 1990. In 2002, the FDA announced clozapine was effective in reducing the ...