Shots:
- The US FDA has approved Yorvipath (QD) tablets for treating hypoparathyroidism patients, with its initial supply planned during Q1’25
- The approval was supported by the P-II (PaTH Forward) as well as P-III (PaTHway) clinical trials conducted worldwide
- Ascendis will further introduce the US Ascendis Signature Access Program (A.S.A.P.) for treatment support & financial assistance during the product launch. In addition, it seeks the US FDA’s approval to market currently manufactured product, will be launched by Q4’24 on approval
Ref: FDA | Image: Ascendis Pharma| Press Release
Related News:- The US FDA Approves Citius Pharmaceuticals’ Lymphir to Treat R/R Cutaneous T-Cell Lymphoma (CTCL)
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