Bristol Myers Squibb Schizophrenia Drug Fails Pivotal Test as an Add-On to Antipsychotics
- Bristol Myers Squibb's drug Cobenfy failed a pivotal Phase 3 trial on Tuesday.
- The test aimed to support expanding Cobenfy's use as an adjunctive schizophrenia treatment.
- Researchers evaluated Cobenfy alongside standard antipsychotics in adults with uncontrolled symptoms.
- Cobenfy showed a numerical improvement but did not achieve statistical significance versus placebo at week six.
- This outcome impacts commercial prospects and prompted analysts to reduce revenue projections for the drug.
15 Articles
15 Articles


Bristol Myers Squibb Schizophrenia Drug Fails Pivotal Test as an Add-On to Antipsychotics
Bristol Myers Squibb’s Cobenfy failed to outdistance a placebo in a Phase 3 test that evaluated the drug as an adjunct to antipsychotics in schizophrenia patients. Last September, the FDA approved Cobenfy as a standalone schizophrenia treatment. The post Bristol Myers Squibb Schizophrenia Drug Fails Pivotal Test as an Add-On to Antipsychotics appeared first on MedCity News.
Bristol Myers Sheds 6% After Promising Schizophrenia Drug Flops In Phase 3 Test
Shares of Bristol Myers Squibb tumbled late Tuesday after the company's schizophrenia drug, Cobenfy, failed in a Phase 3 study. The post Bristol Myers Sheds 6% After Promising Schizophrenia Drug Flops In Phase 3 Test appeared first on Investor's Business Daily.
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