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                                      author：comprehensive   
                                        
                                      
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browse：5338
                                  
                                    
          
                                    
            
          
 
          Eli Lilly headquarters in Indianapolis – pharmaceutical coverage from STAT
          Darron Cummings/AP
          Scientists at the Food and Drug Administration have two big questions about Eli Lilly’s experimental Alzheimer’s drug donanemab ahead of a panel of outside experts that it is convening on Monday:
          Should the patients who receive the medicine be limited based on PET scans of a protein called tau that Eli Lilly used as a key criteria for trying to determine whether they should receive the drug? That could reduce usage of the medicine by adding a barrier to its use.
          advertisement
          And how do the potential risks of using the drug compare to its benefits? The FDA points to one analysis, admittedly with missing data, that could indicate patients who receive the drug have a higher risk of dying.
          STAT+ Exclusive Story
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          Unlock this article — plus daily coverage and analysis of the biotech sector — by subscribing to STAT+.
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