Bristol Myers Squibb gets Reblozyl EC approval for anemia associated with NTD beta thalassemia

Bristol Myers Squibb gets Reblozyl EC approval for anemia associated with NTD beta thalassemia

Bristol Myers Squibb (BMY) has secured full marketing authorization for Reblozyl (luspatercept) from the European Commission (EC) for treating anemia associated with non-transfusion-dependent (NTD) beta thalassemia in adult patients. Presently, Reblozyl is approved in the European Union (EU), the US, and Canada for addressing anemia resulting from transfusion-dependent beta thalassemia and transfusion-dependent lower-risk myelodysplastic syndromes. […]

Novo Nordisk acquires SCD drug developer Forma Therapeutics

Novo Nordisk acquires SCD drug developer Forma Therapeutics

Novo Nordisk acquisition of Forma Therapeutics : Danish pharma company Novo Nordisk has closed the previously announced $1.1 billion acquisition of Forma Therapeutics, a clinical-stage biopharma company focused on developing drugs for the treatment of sickle cell disease (SCD) and rare blood disorders. As per the terms of the deal announced last month, shareholders of […]

Pfizer to acquire Oxbryta developer Global Blood Therapeutics for $5.4bn

Pfizer to acquire Oxbryta developer Global Blood Therapeutics for $5.4bn

Pfizer has agreed to acquire Global Blood Therapeutics (GBT), a publicly-listed American biopharma company, in a deal worth around $5.4 billion with an aim to boost its presence in rare hematology. Global Blood Therapeutics is particularly focused on developing drugs for the treatment of sickle cell disease (SCD). The company’s sickle cell disease drug Oxbryta […]

Agios Pharmaceuticals gets PYRUKYND FDA approval for hemolytic anemia

Agios Pharmaceuticals gets PYRUKYND FDA approval for hemolytic anemia

Agios Pharmaceuticals has secured approval for PYRUKYND (mitapivat) from the US Food and Drug Administration (FDA) for the treatment of hemolytic anemia in adult patients having pyruvate kinase (PK) deficiency. PYRUKYND is an oral pyruvate kinase activator, which is now the first approved disease-modifying therapy for the rare, debilitating, lifelong hemolytic anemia. The FDA approval […]

Celgene, Acceleron bag Reblozyl FDA approval for anemia in beta thalassemia

Celgene, Acceleron bag Reblozyl FDA approval for anemia in beta thalassemia

Reblozyl FDA approval : Celgene and Acceleron Pharma have bagged approval from the US Food and Drug Administration (FDA) for Reblozyl (luspatercept-aamt) for the treatment of anemia associated with beta thalassemia in adults who need regular red blood cell (RBC) transfusions. Reblozyl is now the first and only erythroid maturation agent to be approved by […]

Modus Therapeutics secures $15.7m for sickle cell disease drug development

Modus Therapeutics secures $15.7m for sickle cell disease drug development

Modus Therapeutics, a Swedish biotech firm specializing in sickle cell disease therapies, has successfully raised SEK 140 million ($15.76 million) in a funding round spearheaded by HealthCap, a leading European venture capital firm known for investing in innovative therapies for diseases with significant unmet medical needs. The Series A funding round saw HealthCap contribute SEK […]