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Eliminates hundreds of treatments! Pfizer (PFE.US) gene therapy approved for listing by FDA
Pfizer/PFE.us (Pfizer/PFE.us) announced that the US FDA has approved the single-use gene therapy Beqvez (fidanacogene elaparvovec) it has developed to treat adults with moderate to severe hemophilia B aged 18 or above.
Zhitong Finance04:08 ET
Pfizer Options Spot-On: On April 26th, 118.91K Contracts Were Traded, With 3.21 Million Open Interest
On April 26th ET, $Pfizer(PFE.US)$ had active options trading, with a total trading volume of 118.91K options for the day, of which put options accounted for 37.64% of the total transactions, and call
moomoo News16:30 ET
Sector Update: Health Care Stocks Edge Higher Late Afternoon
Health care stocks were advancing late Friday afternoon, with the NYSE Health Care Index adding 0.2% and the Health Care Select Sector SPDR Fund (XLV) up 0.1%. The iShares Biotechnology ETF (IBB) rose
MT Newswires15:57 ET
Express News | NYSE Order Imbalance 3209310.0 Shares on Sell Side
Reuters15:50 ET
Pfizer is the first gene therapy approved in the US! Treating hemophilia B
On Friday, April 26, the US Food and Drug Administration (FDA) announced that it has officially approved a new drug called Beqvez developed by Pfizer to treat hemophilia B. According to reports, this is the first gene therapy drug approved by Pfizer in the US market. Hemophilia B is a rare hereditary bleeding disorder that mainly affects men. The cause is a lack or complete absence of a blood clotting protein called factor IX in the patient's body. This lack of protein makes it difficult for blood to clot, making patients prone to bruising and prolonged bleeding time. In severe cases, patients can even experience ignorance
wallstreetcn15:24 ET
More Than Half of the S&P 500 Names That Reported Results This Week Beat Top and Bottom Line - Earnings Scorecard
Seeking Alpha15:11 ET
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