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

Insurer access challenges likely lie ahead for the novel schizophrenia drug Cobenfy, given its considerably higher price than ...

AbbVie Inc.’s disappointing trial results for its new schizophrenia drug bode well for rival Bristol Myers Squibb Co., ...

Bristol Myers Squibb Co. shares surged 12.5% Monday after rival AbbVie Inc. reported disappointing results from the trial of ...

Shares in AbbVie slumped Monday after the company disclosed its psychiatric medicine emraclidine didn’t best placebo in two ...

which the U.S. Food and Drug Administration approved for the treatment of schizophrenia in September 2024. (Bristol Myers Squibb via AP) This image provided by Bristol Myers Squibb in October 2024 ...

US pharma group says patients who took Emraclidine in clinical trials failed to show a significant decline in symptoms ...

More recent acquisitions in 2024—oncology firms Mirati and RayzeBio and neurology firm Karuna—also help support Bristol's strong overall pipeline and wide moat. Bristol has created a strong pipeline ...

If it does prove to be the end of emraclidine for schizophrenia, that looks set to benefit Bristol-Myers Squibb, which ended ...

QoL improvements were also significant, as assessed by the Schizophrenia Quality ... and was first approved by the US Food and Drug Administration (FDA) in 2009. It is marketed by Eli Lilly ...

The S&P 500 added 0.1% on Monday, Nov. 11, 2024, closing above the 6,000-point milestone as investors continued to weigh the ...

The Food and Drug Administration approved Cobenfy on the strength of ... “It’s not any higher or any lower than what we ...