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Bristol Myers Squibb to Present Late-Breaking Data for Breyanzi (lisocabtagene maraleucel) in Relapsed or Refractory Follicular Lymphoma and Mantle Cell Lymphoma at 2023 International Conference on Malignant Lymphoma

Pivotal trials TRANSCEND FL and TRANSCEND NHL 001 continue to underscore the transformative potential of Breyanzi and its clinically meaningful benefit across the broadest array of B-cell... | May 30, 2023
Bristol Myers Squibb Frank Morschhauser Michael Wang Anne Kerber International Conference On Malignant Lymphoma Drug Administration

Johnson & Johnson : Janssen Submits New Drug Application to U.S. FDA Seeking Approval of Investigational Single Tablet Combination Therapy of Macitentan and Tadalafil for Treatment of Patients with Pulmonary Arterial Hypertension (PAH)

RARITAN, NJ,May 30, 2023 - The Janssen Pharmaceutical Companies of Johnson & Johnson announced today the submission of a New Drug Application to the U.S. Food and Drug Administration ... | May 30, 2023
Shelly Orlacchio Tina Kitt World Health Organization Group Janssen Research Development Companies Of Johnson European Society Of Cardiology Respiratory

Legend Biotech Corporation: Legend Biotech Announces Submission to the European Medicines Agency for Expanded Use of CARVYKTI (ciltacabtagene autoleucel)

The application to the European Medicines Agency is supported by data from the Phase 3 CARTITUDE-4 study, evaluating the safety and efficacy of cilta-cel in the treatment of patients with relapsed
United States New Jersey Gewinn Nur Ying Huang Hemophagocytic Lymphohistiocytosis Joanne Choi

Legend Biotech Announces Submission to the European Medicines Agency for Expanded Use of CARVYKTI® (ciltacabtagene autoleucel)

The application to the European Medicines Agency is supported by data from the Phase 3 CARTITUDE-4 study, evaluating the safety and efficacy of cilta-cel in the treatment of patients with relapsed... | May 25, 2023
New Jersey United States Hemophagocytic Lymphohistiocytosis Ying Huang Drug Administration European Commission

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Bristol Myers Squibb's Breyanzi (lisocabtagene maraleucel) is First and Only CAR T to Deliver Deep and Durable Efficacy in Pivotal Multicenter Trial in Relapsed or Refractory Chronic Lymphocytic Leukemia, Based on Data Presented at ASCO 2023

TRANSCEND CLL 004 is the first pivotal multicenter trial to evaluate a CAR T cell therapy in heavily pre-treated patients with relapsed or refractory chronic lymphocytic leukemia or small lymphocytic... | May 25, 2023
United States Bristol Myers Squibb Anne Kerber Tanya Siddiqi Division Of Lymphoma American Society Of Clinical Oncology

FDA approves extended-release buprenorphine injection for opioid use disorder

The FDA announced that it has approved Brixadi, an extended-release subcutaneous injection for the treatment of moderate to severe opioid use disorder.Brixadi (buprenorphine, Braeburn Inc.) is the first long-acting buprenorphine injectable that can be given in weekly or monthly doses to patients with opioid use disorder (OUD) who have already initiated treatment with transmucosal buprenorphine or
Shenaz Bagha Robertm Califf Mental Health Services Administration Braeburn Inc Substance Abuse Risk Evaluation
Source: healio.com

ACOG session provides latest updates, guidance on mifepristone availability

BALTIMORE — A special late-breaking session at the ACOG Annual Scientific & Clinical meeting featured the most up-to-date information and guidance on availability of the abortion drug mifepristone. Kristyn M. Brandi, MD, MPH, FACOG, the Darney-Landy Fellow at ACOG for 2022-2023 and OB/GYN physician and complex family planning subspecialist, discussed the current controversy
United States Bykatie Kalvaitis Kristynm Brandi Richard Smith Drug Administration Breaking Updates
Source: healio.com

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