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Cumberland Pharmaceuticals’ Ifetroban Secures the US FDA’s ODD and RPDD for Duchenne Muscular Dystrophy

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Cumberland Pharmaceuticals

Cumberland Pharmaceuticals’ Ifetroban Secures the US FDA’s ODD and RPDD for Duchenne Muscular Dystrophy

Shots:

  • The US FDA has granted ODD & RPDD to ifetroban for treating cardiomyopathy related to Duchenne muscular dystrophy (DMD)
  • Ifetroban (QD, oral) is a selective thromboxane-prostanoid receptor (TPr) antagonist being investigated under P-II (FIGHT DMD) study for its safety, efficacy & PK in DMD patients, with results anticipated during Q4’24
  • The company is also conducting another P-II (FIGHTING FIBROSIS) study for assessing the safety & efficacy of ifetroban vs PBO in patients with idiopathic pulmonary fibrosis (IPF) for over 52wks.

Ref: Cumberland Pharmaceuticals | Image: Cumberland Pharmaceuticals 

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Dipanshu Dixit

A passionate content writer with expertise in delivering high-quality and engaging content, Dipanshu is a keen reader and a versatile writer. Dipanshu dedicatedly covers news ranging from biopharma, life sciences, biotech, and MedTech to diagnostics and animal health companies. He can be contacted at connect@pharmashots.com

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