|Day Low/High||77.70 / 80.07|
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Ultragenyx scored its second FDA drug approval in six months. The orphan disease specialist also picked up its second Rare Pediatric Disease Priority Review Voucher; its first sold for $130 million.
A look at three names to consider in the biotech and biopharma space.
The most recent short interest data has been released for the 01/31/2018 settlement date, which shows a 919,934 share decrease in total short interest for Ultragenyx Pharmaceutical Inc , to 4,819,058, a decrease of 16.03% since 01/12/2018. Total short interest is just one way to look at short data; another metric that we here at Dividend Channel find particularly useful is the "days to cover" metric because it considers both the total shares short and the average daily volume of shares traded.
Newman Ferrara LLP announced today that the firm is conducting an investigation on behalf of shareholders of Ultragenyx Pharmaceutical Inc.
Early Evidence of Normalization of Ureagenesis in One Patient in Lowest-Dose Cohort and Acceptable Initial Safety Profile
Ultragenyx to Provide Additional Information to FDA for Consideration of Possible Early Filing on Current Phase 2 Data
If approved, Burosumab would be the first targeted disease-modifying treatment for XLH
The Cambridge, Mass.-based Ironwood unveiled top-line data from a pair of Phase 2a studies evaluating IW-1973 in patients that have type 2 diabetes and hypertension.
Further improvement in disease symptoms and fracture healing observed through 48 weeks of treatment with burosumab
The hotly debated tax reform championed by the Trump White House needs to be paid for by spending cuts. One proposed change could eliminate the tax credit for companies developing treatments through the Orphan Drug Act.
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First Cohort Data Expected in Early 2018
Ultragenyx to Host Conference Call Today at 5:00pm ET
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