FDA Approves New Formulation of Hyrimoz Adalimumab Biosimilar

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FDA Approves New Formulation of Hyrimoz Adalimumab Biosimilar
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The FDA approved a citrate-free, 100 mg/mL formulation of the biosimilar adalimumab-adaz TwitteRx RheumTwitter

The US Food and Drug Administration has approved a citrate-free, 100 mg/mL formulation of the biosimilar adalimumab-adaz , according to aHyrimoz, a tumor necrosis factor blocker that is biosimilar to its reference product Humira, was approved by the FDA in 2018 at a concentration of 50 mg/mL for rheumatoid arthritis, juvenile idiopathic arthritis, psoriatic arthritis, ankylosing spondylitis, Crohn's disease, ulcerative colitis, and plaque psoriasis.

Sandoz said that it intends to launch the citrate-free formulation in the United States on July 1. It will be one of up to nine other adalimumab biosimilars that are expected to launch in July. On January 31, Amjevita became the

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