Jubbonti® (denosumab-bddz)

news

European Commission grants first-of-a-kind biosimilar approval

22 May 2024 | By Catherine Eckford (European Pharmaceutical Review)

The approval means Sandoz’s Wyost® and Jubbonti® are the first biosimilars of denosumab authorised in Europe.

news

CHMP meeting highlights: March 2024

26 March 2024 | By Catherine Eckford (European Pharmaceutical Review)

At the Committee for Medicinal Products for Human Use (CHMP)’s March meeting, twelve medicines received positive opinions for marketing authorisations, including a new antibiotic and a novel oral medicine for a rare blood disorder.

news

Sandoz granted novel biosimilars approval

6 March 2024 | By Catherine Eckford (European Pharmaceutical Review)

The approval authorises the interchangeability of denosumab biosimilars in the US to treat primary and secondary bone loss.

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Recommended

Jubbonti® (denosumab-bddz)

European Commission grants first-of-a-kind biosimilar approval

CHMP meeting highlights: March 2024

Sandoz granted novel biosimilars approval