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Bristol Myers Squibb to Present Data at ASCO & EHA from More Than 130 Studies Across 25 Diseases Supporting Expansion into New Indications, Demonstrating Long-Term Survival, and Highlighting Novel Modalities and Research Platforms

Bristol Myers Squibb (NYSE: BMY) today announced the presentation of data across its oncology and hematology portfolio at the upcoming 2024 American Society of Clinical Oncology (ASCO) Annual Meeting

Libervant Buccal Film Approved for Seizure Clusters in Patients 2 to 5 Years Old

The approval was based on safety and efficacy data from clinical trials evaluating diazepam rectal gel, as well as adult bioavailability studies comparing Libervant with diazepam rectal gel, adult and pediatric pharmacokinetic data, and an open-label safety study of Libervant.

Libervant Buccal Film Approved for Seizure Clusters in Patients 2 to 5 Years Old

The approval was based on safety and efficacy data from clinical trials evaluating diazepam rectal gel, as well as adult bioavailability studies comparing Libervant with diazepam rectal gel, adult and pediatric pharmacokinetic data, and an open-label safety study of Libervant.

Vanda Pharmaceuticals Fanapt® (iloperidone) Receives U S FDA Approval for the Acute Treatment of Bipolar I Disorder

Vanda Pharmaceuticals Fanapt® (iloperidone) Receives U S FDA Approval for the Acute Treatment of Bipolar I Disorder
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Vanda Pharmaceuticals Fanapt® (iloperidone) Receives U S FDA Approval for the Acute Treatment of Bipolar I Disorder

Vanda Pharmaceuticals Fanapt® (iloperidone) Receives U S FDA Approval for the Acute Treatment of Bipolar I Disorder
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