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-0.000621491200132176 -0.000277174745765365 0.000239299935784974 -0.00165444056323285 0.00230519866198633 -0.00217091524478319 -0.00217091524478319 -0.00217091524478319
Stock impact report

bluebird (BLUE) Underperforms Industry YTD Amid Challenges [Yahoo! Finance]

CRISPR Therapeutics AG - Common Shares (CRSP) 
Last crispr therapeutics ag - common shares earnings: 8/7 05:01 pm Check Earnings Report
US:NASDAQ Investor Relations: nasdaq.com/symbol/crsp/real-time
Company Research Source: Yahoo! Finance
While the approval of its three gene therapies bodes well, the uptake of the same has not gained traction as expected. Image Source: Zacks Investment Research The FDA approved Zynteglo for the treatment of beta-thalassemia in adult and pediatric patients requiring regular red blood cell transfusion on Aug 17, 2022. It also approved Skysona for treating early, active cerebral adrenoleukodystrophy on Sep 16, 2022. The FDA recently approved its third gene therapy, lovotibeglogene autotemcel (lovo-cel), under the brand name Lyfgenia, for the treatment of sickle cell disease (SCD) in patients aged 12 years and older with a history of vaso-occlusive events. However, revenues in 2023 totaled only $29.5 million. Of this amount, $16.7 million was attributable to Zynteglo and $12.4 million to Skysona, with gross-to-net discounts of 19% across both products. bluebird anticipates 85-105 patient starts (cell collections), combined across all three of its FDA-approved therapies (Lyfgenia, Show less Read more
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