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Novo Nordisk to Buy Forma Therapeutics for $1.1 Billion

Novo Nordisk to Buy Forma Therapeutics for $1.1 Billion

  • Posted by ISPE Boston
  • On September 8, 2022

Watertown-based Forma Therapeutics, a clinical-stage biopharma focused on sickle cell disease (SCD) and rare blood disorders, is being acquired by Novo Nordisk for $1.1 billion. The acquisition includes Forma’s lead development candidate, etavopivat, and is aligned with Novo Nordisk’s strategy to complement and accelerate its scientific presence and pipeline in hemoglobinopathies, a group of disorders in which there is abnormal production or structure of the hemoglobin protein in the red blood cells. The transaction is expected to close in the fourth quarter of 2022.

The FDA has granted etavopivat Fast Track, Rare Pediatric Disease and Orphan Drug designations. Additionally, etavopivat was granted Orphan Drug designation from the European Commission based on a positive opinion from the Committee for Orphan Medicinal Products of the European Medicines Agency for the treatment of patients with SCD.

Sickle cell disease (SCD) is a chronic and progressive inherited disorder associated with a decrease in the health and lifespan of red blood cells. People living with SCD have red blood cells that are crescent shaped, rendering them inflexible, fragile, and unable to effectively deliver oxygen. The health of these sickle red blood cells is impaired and characterized by reduced cellular energy, poor deformability, decreased membrane repair, and increased adhesion.

Around 17 million people worldwide live with SCD, including approximately 100,000 people in the United States, as well as approximately 30,000 in France, Germany, Italy, Spain, and the United Kingdom. Despite recent advances in treatment, most patients with SCD still suffer from pain crises, lifelong disability, reduced quality of life, and shortened life expectancy.

Etavopivat, a selective pyruvate kinase-R (PKR) activator, works by activating the red blood cell’s natural PKR activity, allowing sickle hemoglobin to hold on to oxygen longer and resulting in decreased polymerization, hemolysis, and sickling. Etavopivat-mediated PKR activation also increases adenosine triphosphate (ATP) levels, to improve red blood cell function, which can lead to improved deformability, capacity for membrane repair, red blood cell health, and lifespan. Together, these effects are anticipated to improve the health of sickle red blood cell and lead to a reduction in anemia, hemolysis, vaso-occlusive crises, and end organ damage. (Source: Forma Therapeutics Website, 01 September, 2022)

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