Bristol-Myers Squibb received FDA's approval for Cobenfy, which is poised to be a game changer in the treatment of ...
PureTech Health has obtained approval from the US Food and Drug Administration (FDA) for KarXT to treat schizophrenia in ...
In a phase II trial of moderate-to-severe major depressive disorder, 6 weeks of intensive treatment with psilocybin or ...
The medication is the first in decades to have a different mode of action than do current drugs, achieving better symptom ...
After more than three decades, schizophrenia patients have a new treatment option. The US FDA has approved a drug, known as ...
Bristol Myers Squibb's drug, KarXT, improved symptoms of adults with schizophrenia and had fewer side effects than antipsychotic treatments ...
This approval triggers 2 milestone payments totaling $29 million, as per agreements with Royalty Pharma and PureTech's founded entity, Karuna Therapeutics, which was acquired by Bristol Myers Squibb ...
Nine years on from securing $3.84 million for a phase I clinical trial to test the formulation, with results showing it ...
KarXT — now with the brand name Cobenfy— is expected to be available in October with a list price of about $22,500 annually.
Invented KarXT Receives U.S. Food and Drug Administration Approval for the Treatment of Schizophrenia in Adults ...
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