BRISTOL MYERS SQUIBB

🇫🇷France
Ownership
-
Established
1989-01-01
Employees
30K
Market Cap
$97.5B
Website
https://www.bms.com/
msn.com
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Bristol-Myers Squibb Gets FDA Approval for Schizophrenia Drug

The article discusses the importance of SSR (Server-Side Rendering) in modern web development, emphasizing its role in improving performance and user experience.
reason.com
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In a Victory for the Free Market, FDA Approves New Schizophrenia Drug

The FDA approved a novel antipsychotic schizophrenia drug, Cobenfy, targeting cholinergic receptors to reduce side effects like weight gain and cognitive impairment. Cobenfy's monthly cost is $1,850, marking a market-driven win over government-funded research, which has yet to significantly benefit patients.
psychiatrictimes.com
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Poll: Do You Feel Prepared to Prescribe the Newly Approved First-In-Class Muscarinic Agonist?

The FDA approved Cobenfy (xanomeline and trospium chloride) for schizophrenia, marking the first novel mechanism in decades, targeting M1 and M4 receptors without blocking D2. Bristol Myers Squibb's CEO highlights the potential to change the treatment paradigm.
kacu.org
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A new kind of drug for schizophrenia promises fewer side effects

The FDA approved Cobenfy, a new schizophrenia drug with fewer side effects than current treatments, targeting muscarinic receptors instead of dopamine. Marketed by Bristol Myers Squibb, it will be available from October at $1,850 a month, pending insurance coverage. While initial studies are promising, long-term safety and efficacy remain uncertain.
pharmacytimes.com
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FDA Approves Cobenfy, Previously KarXT, for Treatment of Schizophrenia

The FDA approved xanomeline and trospium chloride (Cobenfy) for schizophrenia in adults, marking the first in a new class targeting M1 and M2 receptors without blocking D2 receptors. Supported by the EMERGENT clinical program, Cobenfy demonstrated a statistically significant 8.4-point reduction in PANSS scores compared to placebo, with generally well-tolerated safety profile.
qz.com
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The FDA just approved Bristol Myers Squibb's groundbreaking schizophrenia treatment

FDA approves Bristol Myers Squibb's Cobenfy, the first novel schizophrenia treatment in 70 years, targeting muscarinic receptors to reduce dopamine activity without typical antipsychotic side effects. Expected to launch in late October at $22,500/year, with potential peak U.S. sales of $2 billion by 2030.
seekingalpha.com
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Unlocking Value With KarXT (Cobenfy) FDA Approval

Biologist with M.Sc in Biomedicine, PhD in Bioengineerings, and 20+ years in Cell & Gene Therapies (CGT) research and development, focusing on biotech, pharma, Medtech, and healthcare stocks analysis. Long position in BMY shares. Independent SA analyst adhering to Seeking Alpha’s guidelines.
investors.com
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Bristol-Myers Squibb Schizophrenia Drug Wins FDA Approval; BMY Stock Signals Breakout

Bristol-Myers Squibb's novel schizophrenia drug, Cobenfy, received FDA approval. Cobenfy, the first non-dopamine blocking treatment, aims to reduce side effects. Acquired from Karuna Therapeutics for $14 billion, the twice-daily pill will cost $1,850 monthly. BMY stock rose 4.35% to 52.30, signaling a breakout.
nbcrightnow.com
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FDA Approves New Kind of Drug for Schizophrenia

The FDA approved Cobenfy, the first new schizophrenia medication in decades, targeting a new neurochemical pathway via cholinergic receptors to reduce symptoms without typical dopamine-focused drug side effects like weight gain and sluggishness. Cobenfy's short-term trials showed symptom reduction, but long-term effectiveness and safety remain uncertain. The drug, priced at $1,850/month, does not carry atypical antipsychotic class warnings.
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