Horizon’s Procysbi (Cysteamine Bitartrate) Receives the US FDA’s Approval for Delayed Release Oral Tablets
Horizon Therapeutics’ Tepezza (teprotumumab-trbw) Receives the US FDA’s Approval as the First Therapy for Thyroid Eye Disease
Shots:
- The US FDA has approved Procysbi for adults and children one year of age and older living with nephropathic cystinosis
- Procysbi (cysteamine bitartrate) is a delayed-release capsules and delayed-release oral granules also a cystine-depleting agent indicated to treat nephropathic cystinosis in adults and pediatric patients 1 year of age and older
- Procysbi will continue to be available in 25 mg and 75 mg strengths while the 75mg and 300mg is expected to be available in H1’20
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