BioMarin to Acquire Amicus Therapeutics in $4.8 Billion Deal, Bolstering Leadership in Rare Diseases and Driving Growth

BioMarin to Acquire Amicus Therapeutics for $4.8 Billion, Bolstering Leadership in Rare Diseases, Driving Revenue Growth, and Enhancing Financial Outlook BioMarin Pharmaceutical Inc. and Amicus Therapeutics announced today that BioMarin…

Read MoreBioMarin to Acquire Amicus Therapeutics in $4.8 Billion Deal, Bolstering Leadership in Rare Diseases and Driving Growth

BioNTech Completes Acquisition of CureVac N.V., Including Follow-on Offering, to Bolster Leadership in mRNA Innovation

BioNTech Completes Acquisition of CureVac N.V., Including Follow-on Offering Period, to Bolster Its Leading Position in the mRNA Space BioNTech SE today announced the closing of its acquisition of CureVac N.V…

Read MoreBioNTech Completes Acquisition of CureVac N.V., Including Follow-on Offering, to Bolster Leadership in mRNA Innovation

Johnson & Johnson Secures FDA Approval for TRUFILL n-BCA Liquid Embolic System to Treat Symptomatic Chronic Subdural Hematoma

Johnson & Johnson Secures FDA Approval for TRUFILL n-BCA Liquid Embolic System to Treat Symptomatic Chronic Subdural Hematoma Johnson & Johnson MedTech, a leader in neurovascular care, announced that the U.S.…

Read MoreJohnson & Johnson Secures FDA Approval for TRUFILL n-BCA Liquid Embolic System to Treat Symptomatic Chronic Subdural Hematoma

Novo Nordisk Seeks FDA Approval for CagriSema—First Once-Weekly Combination of GLP-1 and Amylin Analogues for Weight Management

Novo Nordisk Submits FDA Application for CagriSema—First Once-Weekly Combination of GLP-1 and Amylin Analogues for Weight Management Today, Novo Nordisk announced the submission of a New Drug Application (NDA) to…

Read MoreNovo Nordisk Seeks FDA Approval for CagriSema—First Once-Weekly Combination of GLP-1 and Amylin Analogues for Weight Management

Incyte Announces EC Approval of Minjuvi® (Tafasitamab) for Relapsed or Refractory Follicular Lymphoma

Incyte Announces EU Approval of Minjuvi® for R/R Follicular Lymphoma Incyte today announced that the European Commission (EC) has approved Minjuvi® (tafasitamab) in combination with lenalidomide and rituximab for the treatment of adult…

Read MoreIncyte Announces EC Approval of Minjuvi® (Tafasitamab) for Relapsed or Refractory Follicular Lymphoma