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Amneal Pharmaceuticals’s Releuko (biosimilar, filgrastim) Receives the US FDA’s Approval of BLA for the Treatment of Neutropenia

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Amneal Pharmaceuticals’s Releuko (biosimilar, filgrastim) Receives the US FDA’s Approval of BLA for the Treatment of Neutropenia

Shots:

  • The US FDA has approved the BLA for filgrastim-ayow, a biosimilar referencing Neupogen to treat neutropenia. Releuko has been developed in collaboration with Kashiv & will be marketed under the name Releuko
  • The company is expected to launch Releuko in Q3’22 along with a full patient support program & is planning to launch pegfilgrastim biosimilar referencing Neulasta and a bevacizumab biosimilar referencing Avastin in 2022
  • Releuko is supplied in single-dose vials & prefilled syringes containing 300/480mcg of filgrastim-ayow in a preservative-free solution

Ref: Amneal | Image: Amneal

Click here to­ read the full press release 

Senior Editor

Neha is a Senior Editor at PharmaShots. She is passionate and very enthusiastic about recent updates and developments in the life sciences and pharma industry. She covers Biopharma, MedTech, and Digital health segments along with different reports at PharmaShots. She can be contacted at connect@pharmashots.com.

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