AbbVie Wins EU Approval for TEPKINLY in Combination with Lenalidomide and Rituximab
The European Commission has approved AbbVie's TEPKINLY with lenalidomide and rituximab as the first bispecific, chemotherapy-free treatment for Relapsed or Refractory Follicular Lymphoma in the second-line setting.
Roopal Thakkar | 07/07/2026 | By News Bureau
European Commission Approves AbbVie's MAVIRET for Acute Hepatitis C
The European Commission (EC) has approved AbbVie’s MAVIRET for acute Hepatitis C Virus (HCV) infection, enabling earlier treatment initiation to help reduce disease progression, cirrhosis, and liver cancer risk.
Roopal Thakkar | 24/06/2026 | By News Bureau
EU Approves AQUIPTA for Acute Migraine Treatment in Adults
The EC has approved AQUIPTA (atogepant) for the acute treatment and prevention of migraine in adults, based on phase 3 ECLIPSE trial results demonstrating rapid pain relief, sustained efficacy, and consistent benefits across multiple migraine attacks. The approval expands AbbVie’s migraine treatment portfolio across EU.
Roopal Thakkar | 03/06/2026 | By News Bureau | 109
US FDA Approves DECNUPAZ for Treatment of Blastic Plasmacytoid Dendritic Cell Neoplasm
AbbVie has received US FDA approval for DECNUPAZ to treat adults with Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN), marking the first and only outpatient-initiated ADC for BPDCN and AbbVie’s first approved Antibody Drug Conjugate (ADC) for hematologic malignancies.
Roopal Thakkar | 30/05/2026 | By News Bureau | 122
AbbVie to Acquire Gilgamesh's Psychedelic Antidepressant Bretisilocin in USD 1.2 Billion Deal
AbbVie has announced a USD 1.2 billion deal to acquire Gilgamesh Pharmaceuticals’ lead candidate bretisilocin, a next-generation psychedelic compound in clinical development for treating moderate-to-severe major depressive disorder.
Roopal Thakkar | 26/08/2025 | By Mrinmoy Dey | 226
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