- Company says it has completed its rolling submission of an NDA to the FDA for setmelanotide for the treatment of pro-opiomelanocortin deficiency obesity and leptin receptor deficiency obesity
- Rhythm has requested priority review for the application which, if granted, could provide a target FDA review period of six months from the application filing date
- Company continues to anticipate that it will submit a Marketing Authorization Application to the
European Medicines Agency in the second quarter of 2020 - Says ...
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